rs138619017 |
47126807 |
G |
J40-J47 Chronic lower respiratory diseases |
0.004338 |
0.33989 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
G25 Other extrapyramidal and movement disorders |
0.00030432 |
0.64912 |
0.003692 |
0.01803 |
genotyped |
1.23 |
rs138619017 |
47126807 |
G |
G20 Parkinson's disease |
0.0012391 |
0.17257 |
0.003692 |
0.01803 |
genotyped |
1.57 |
rs138619017 |
47126807 |
G |
L72 Follicular cysts of skin and subcutaneous tissue |
0.00022373 |
0.92647 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
oesophageal disorder |
-0.0041937 |
0.3195 |
0.003692 |
0.01803 |
genotyped |
0.935 |
rs138619017 |
47126807 |
G |
bacterial infection |
-6.9441e-05 |
0.96812 |
0.003692 |
0.01803 |
genotyped |
0.993 |
rs138619017 |
47126807 |
G |
psychological/psychiatric problem |
-0.010223 |
0.023373 |
0.003692 |
0.01803 |
genotyped |
0.864 |
rs138619017 |
47126807 |
G |
J34 Other disorders of nose and nasal sinuses |
0.0030591 |
0.15902 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
H15-H22 Disorders of sclera, cornea, iris and ciliary body |
0.0009309 |
0.39385 |
0.003692 |
0.01803 |
genotyped |
1.27 |
rs138619017 |
47126807 |
G |
O26 Maternal care for other conditions predominantly related to pregnancy |
0.0031336 |
0.12835 |
0.003692 |
0.01803 |
genotyped |
1.48 |
rs138619017 |
47126807 |
G |
O20 Haemorrhage in early pregnancy |
0.00018458 |
0.90154 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
heart valve problem/heart murmur |
-0.0032268 |
0.036052 |
0.003692 |
0.01803 |
genotyped |
0.661 |
rs138619017 |
47126807 |
G |
O94-O99 Other obstetric conditions, not elsewhere classified |
0.0030058 |
0.1428 |
0.003692 |
0.01803 |
genotyped |
1.47 |
rs138619017 |
47126807 |
G |
other fractures |
0.00044099 |
0.52988 |
0.003692 |
0.01803 |
genotyped |
1.31 |
rs138619017 |
47126807 |
G |
glaucoma |
0.00076632 |
0.65717 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
O20-O29 Other maternal disorders predominantly related to pregnancy |
0.0027384 |
0.30208 |
0.003692 |
0.01803 |
genotyped |
1.23 |
rs138619017 |
47126807 |
G |
A30-A49 Other bacterial diseases |
0.0042637 |
0.022653 |
0.003692 |
0.01803 |
genotyped |
1.45 |
rs138619017 |
47126807 |
G |
K44 Diaphragmatic hernia |
-0.0016131 |
0.69903 |
0.003692 |
0.01803 |
genotyped |
0.974 |
rs138619017 |
47126807 |
G |
K40 Inguinal hernia |
-0.0019106 |
0.54922 |
0.003692 |
0.01803 |
genotyped |
0.949 |
rs138619017 |
47126807 |
G |
K41 Femoral hernia |
0.00030628 |
0.65172 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
K42 Umbilical hernia |
9.6642e-06 |
0.99528 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
K43 Ventral hernia |
0.0012892 |
0.40971 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
G51 Facial nerve disorders |
-3.3851e-05 |
0.96597 |
0.003692 |
0.01803 |
genotyped |
0.984 |
rs138619017 |
47126807 |
G |
G57 Mononeuropathies of lower limb |
-0.001218 |
0.2678 |
0.003692 |
0.01803 |
genotyped |
0.737 |
rs138619017 |
47126807 |
G |
G56 Mononeuropathies of upper limb |
-0.00064365 |
0.81213 |
0.003692 |
0.01803 |
genotyped |
0.975 |
rs138619017 |
47126807 |
G |
G55 Nerve root and plexus compressions in diseases classified elsewhere |
-0.0021537 |
0.20232 |
0.003692 |
0.01803 |
genotyped |
0.797 |
rs138619017 |
47126807 |
G |
gastric/stomach ulcers |
-0.0039528 |
0.0071467 |
0.003692 |
0.01803 |
genotyped |
0.574 |
rs138619017 |
47126807 |
G |
E66 Obesity |
0.0013248 |
0.62544 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
M05-M14 Inflammatory polyarthropathies |
0.0047995 |
0.17893 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
mumps / epidemic parotitis |
-0.0007927 |
0.32401 |
0.003692 |
0.01803 |
genotyped |
0.689 |
rs138619017 |
47126807 |
G |
other renal/kidney problem |
0.00054258 |
0.67125 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
G40-G47 Episodic and paroxysmal disorders |
0.00085922 |
0.78474 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
G00-G09 Inflammatory diseases of the central nervous system |
-0.00061788 |
0.35763 |
0.003692 |
0.01803 |
genotyped |
0.659 |
rs138619017 |
47126807 |
G |
J22 Unspecified acute lower respiratory infection |
-0.000573 |
0.80493 |
0.003692 |
0.01803 |
genotyped |
0.968 |
rs138619017 |
47126807 |
G |
hypothyroidism/myxoedema |
0.0033599 |
0.33678 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium |
0.0016777 |
0.34357 |
0.003692 |
0.01803 |
genotyped |
1.34 |
rs138619017 |
47126807 |
G |
D73 Diseases of spleen |
7.8757e-05 |
0.89919 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
D70 Agranulocytosis |
0.0042181 |
0.0058529 |
0.003692 |
0.01803 |
genotyped |
1.73 |
rs138619017 |
47126807 |
G |
B25-B34 Other viral diseases |
-0.00042423 |
0.72059 |
0.003692 |
0.01803 |
genotyped |
0.912 |
rs138619017 |
47126807 |
G |
epilepsy |
0.0016339 |
0.2993 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
D75 Other diseases of blood and blood-forming organs |
5.6031e-06 |
0.99337 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
N92 Excessive, frequent and irregular menstruation |
-0.0025938 |
0.62828 |
0.003692 |
0.01803 |
genotyped |
0.954 |
rs138619017 |
47126807 |
G |
N93 Other abnormal uterine and vaginal bleeding |
0.002445 |
0.43757 |
0.003692 |
0.01803 |
genotyped |
1.15 |
rs138619017 |
47126807 |
G |
N90 Other noninflammatory disorders of vulva and perineum |
0.0006691 |
0.7552 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
N97 Female infertility |
0.00067949 |
0.66378 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
N94 Pain and other conditions associated with female genital organs and menstrual cycle |
-0.0051055 |
0.072986 |
0.003692 |
0.01803 |
genotyped |
0.709 |
rs138619017 |
47126807 |
G |
N95 Menopausal and other perimenopausal disorders |
-4.2347e-05 |
0.99311 |
0.003692 |
0.01803 |
genotyped |
0.999 |
rs138619017 |
47126807 |
G |
F05 Delirium, not induced by alcohol and other psychoactive substances |
-0.00076824 |
0.23463 |
0.003692 |
0.01803 |
genotyped |
0.572 |
rs138619017 |
47126807 |
G |
D51 Vitamin B12 deficiency anaemia |
0.0016144 |
0.043801 |
0.003692 |
0.01803 |
genotyped |
2.14 |
rs138619017 |
47126807 |
G |
hiatus hernia |
-0.0030303 |
0.23978 |
0.003692 |
0.01803 |
genotyped |
0.874 |
rs138619017 |
47126807 |
G |
L20-L30 Dermatitis and eczema |
0.0012457 |
0.40848 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
eczema/dermatitis |
0.0018561 |
0.49323 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
other neurological problem |
0.0031864 |
0.12124 |
0.003692 |
0.01803 |
genotyped |
1.26 |
rs138619017 |
47126807 |
G |
M70-M79 Other soft tissue disorders |
-0.0030656 |
0.47147 |
0.003692 |
0.01803 |
genotyped |
0.952 |
rs138619017 |
47126807 |
G |
gastritis/gastric erosions |
0.00028198 |
0.68175 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
I51 Complications and ill-defined descriptions of heart disease |
0.00056748 |
0.74282 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
I50 Heart failure |
0.0022041 |
0.2599 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
N03 Chronic nephritic syndrome |
-0.00091397 |
0.2495 |
0.003692 |
0.01803 |
genotyped |
0.645 |
rs138619017 |
47126807 |
G |
N02 Recurrent and persistent haematuria |
0.00080088 |
0.26449 |
0.003692 |
0.01803 |
genotyped |
1.6 |
rs138619017 |
47126807 |
G |
H18 Other disorders of cornea |
1.0724e-05 |
0.98747 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
C43 Malignant melanoma of skin |
0.0012814 |
0.31622 |
0.003692 |
0.01803 |
genotyped |
1.27 |
rs138619017 |
47126807 |
G |
M24 Other specific joint derangements |
0.0002155 |
0.87534 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
H11 Other disorders of conjunctiva |
-6.4571e-06 |
0.99308 |
0.003692 |
0.01803 |
genotyped |
0.996 |
rs138619017 |
47126807 |
G |
M20 Acquired deformities of fingers and toes |
0.00075571 |
0.77054 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
M21 Other acquired deformities of limbs |
-0.00038246 |
0.73074 |
0.003692 |
0.01803 |
genotyped |
0.91 |
rs138619017 |
47126807 |
G |
M22 Disorders of patella |
0.00088231 |
0.28513 |
0.003692 |
0.01803 |
genotyped |
1.48 |
rs138619017 |
47126807 |
G |
M23 Internal derangement of knee |
0.006053 |
0.06056 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions |
-0.0009751 |
0.479 |
0.003692 |
0.01803 |
genotyped |
0.856 |
rs138619017 |
47126807 |
G |
kidney stone/ureter stone/bladder stone |
-0.0010794 |
0.4772 |
0.003692 |
0.01803 |
genotyped |
0.87 |
rs138619017 |
47126807 |
G |
carpal tunnel syndrome |
-0.0002229 |
0.74993 |
0.003692 |
0.01803 |
genotyped |
0.871 |
rs138619017 |
47126807 |
G |
breast disease (not cancer) |
0.0017816 |
0.52165 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
D86 Sarcoidosis |
0.0001003 |
0.87239 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
O60-O75 Complications of labour and delivery |
0.0043774 |
0.30161 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
gynaecological disorder (not cancer) |
0.0045247 |
0.48124 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
E50-E64 Other nutritional deficiencies |
0.00070623 |
0.48314 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
J95-J99 Other diseases of the respiratory system |
-0.0011496 |
0.55792 |
0.003692 |
0.01803 |
genotyped |
0.914 |
rs138619017 |
47126807 |
G |
depression |
-0.0053877 |
0.17668 |
0.003692 |
0.01803 |
genotyped |
0.906 |
rs138619017 |
47126807 |
G |
K90-K93 Other diseases of the digestive system |
-0.00026167 |
0.92989 |
0.003692 |
0.01803 |
genotyped |
0.991 |
rs138619017 |
47126807 |
G |
E05 Thyrotoxicosis [hyperthyroidism] |
-0.0012408 |
0.28242 |
0.003692 |
0.01803 |
genotyped |
0.755 |
rs138619017 |
47126807 |
G |
pleurisy |
0.00011871 |
0.90702 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
K35 Acute appendicitis |
-0.00056661 |
0.69653 |
0.003692 |
0.01803 |
genotyped |
0.922 |
rs138619017 |
47126807 |
G |
gestational hypertension/pre-eclampsia |
0.00075359 |
0.70851 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
B98 Other specified infectious agents as the cause of diseases classified to other chapters |
-0.00036344 |
0.64347 |
0.003692 |
0.01803 |
genotyped |
0.836 |
rs138619017 |
47126807 |
G |
B96 Other bacterial agents as the cause of diseases classified to other chapters |
-0.0069081 |
0.0057068 |
0.003692 |
0.01803 |
genotyped |
0.717 |
rs138619017 |
47126807 |
G |
B97 Viral agents as the cause of diseases classified to other chapters |
-0.0007674 |
0.22204 |
0.003692 |
0.01803 |
genotyped |
0.554 |
rs138619017 |
47126807 |
G |
B95 Streptococcus and staphylococcus as the cause of diseases classified to other chapters |
0.0011885 |
0.48862 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
L00-L08 Infections of the skin and subcutaneous tissue |
0.0010853 |
0.69113 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
D37-D48 Neoplasms of uncertain or unknown behaviour |
0.00077941 |
0.4958 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
cerebrovascular disease |
0.00029013 |
0.90102 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
K20-K31 Diseases of oesophagus, stomach and duodenum |
-0.0081855 |
0.16879 |
0.003692 |
0.01803 |
genotyped |
0.937 |
rs138619017 |
47126807 |
G |
F10 Mental and behavioural disorders due to use of alcohol |
0.0038093 |
0.049914 |
0.003692 |
0.01803 |
genotyped |
1.35 |
rs138619017 |
47126807 |
G |
I69 Sequelae of cerebrovascular disease |
-0.0011532 |
0.22689 |
0.003692 |
0.01803 |
genotyped |
0.68 |
rs138619017 |
47126807 |
G |
N30-N39 Other diseases of urinary system |
-0.00050388 |
0.90898 |
0.003692 |
0.01803 |
genotyped |
0.992 |
rs138619017 |
47126807 |
G |
H25-H28 Disorders of lens |
0.0037157 |
0.30618 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
disc problem |
-0.0045789 |
0.053381 |
0.003692 |
0.01803 |
genotyped |
0.784 |
rs138619017 |
47126807 |
G |
mania/bipolar disorder/manic depression |
-0.00088324 |
0.33441 |
0.003692 |
0.01803 |
genotyped |
0.728 |
rs138619017 |
47126807 |
G |
I74 Arterial embolism and thrombosis |
0.0010351 |
0.20558 |
0.003692 |
0.01803 |
genotyped |
1.6 |
rs138619017 |
47126807 |
G |
I72 Other aneurysm |
0.0011237 |
0.057076 |
0.003692 |
0.01803 |
genotyped |
2.67 |
rs138619017 |
47126807 |
G |
L43 Lichen planus |
9.7319e-05 |
0.87862 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
angina |
0.0052578 |
0.074212 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
E27 Other disorders of adrenal gland |
-0.00067037 |
0.25076 |
0.003692 |
0.01803 |
genotyped |
0.55 |
rs138619017 |
47126807 |
G |
A00-A09 Intestinal infectious diseases |
0.0047298 |
0.059643 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
E21 Hyperparathyroidism and other disorders of parathyroid gland |
0.0010723 |
0.16233 |
0.003692 |
0.01803 |
genotyped |
1.74 |
rs138619017 |
47126807 |
G |
measles / morbillivirus |
-0.00016505 |
0.86885 |
0.003692 |
0.01803 |
genotyped |
0.951 |
rs138619017 |
47126807 |
G |
O80 Single spontaneous delivery |
-0.0010435 |
0.63368 |
0.003692 |
0.01803 |
genotyped |
0.89 |
rs138619017 |
47126807 |
G |
O82 Single delivery by Caesarean section |
-0.00036745 |
0.75177 |
0.003692 |
0.01803 |
genotyped |
0.861 |
rs138619017 |
47126807 |
G |
H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction |
-9.6907e-05 |
0.94736 |
0.003692 |
0.01803 |
genotyped |
0.986 |
rs138619017 |
47126807 |
G |
G20-G26 Extrapyramidal and movement disorders |
0.0011572 |
0.33207 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
urinary tract infection/kidney infection |
0.0022914 |
0.079447 |
0.003692 |
0.01803 |
genotyped |
1.5 |
rs138619017 |
47126807 |
G |
O16 Unspecified maternal hypertension |
0.00099944 |
0.40719 |
0.003692 |
0.01803 |
genotyped |
1.46 |
rs138619017 |
47126807 |
G |
other respiratory problems |
0.0013711 |
0.45358 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
M91-M94 Chondropathies |
-0.0012721 |
0.17535 |
0.003692 |
0.01803 |
genotyped |
0.645 |
rs138619017 |
47126807 |
G |
appendicitis |
-0.0004777 |
0.76124 |
0.003692 |
0.01803 |
genotyped |
0.944 |
rs138619017 |
47126807 |
G |
D50-D53 Nutritional anaemias |
0.0033477 |
0.17531 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
K00-K14 Diseases of oral cavity, salivary glands and jaws |
-0.0012594 |
0.70267 |
0.003692 |
0.01803 |
genotyped |
0.966 |
rs138619017 |
47126807 |
G |
L30 Other dermatitis |
0.00035504 |
0.73535 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
M60-M63 Disorders of muscles |
0.00031695 |
0.72746 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
allergy/hypersensitivity/anaphylaxis |
0.0034691 |
0.43337 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
F41 Other anxiety disorders |
0.0011821 |
0.56631 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
F40 Phobic anxiety disorders |
0.0010823 |
0.090478 |
0.003692 |
0.01803 |
genotyped |
2.24 |
rs138619017 |
47126807 |
G |
F43 Reaction to severe stress, and adjustment disorders |
0.00065357 |
0.28749 |
0.003692 |
0.01803 |
genotyped |
1.69 |
rs138619017 |
47126807 |
G |
K31 Other diseases of stomach and duodenum |
-0.0012357 |
0.58677 |
0.003692 |
0.01803 |
genotyped |
0.931 |
rs138619017 |
47126807 |
G |
K30 Dyspepsia |
-0.0006135 |
0.83266 |
0.003692 |
0.01803 |
genotyped |
0.978 |
rs138619017 |
47126807 |
G |
M48 Other spondylopathies |
0.00041724 |
0.80673 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
other abdominal problem |
0.0012907 |
0.51017 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
N48 Other disorders of penis |
-0.0022 |
0.4126 |
0.003692 |
0.01803 |
genotyped |
0.816 |
rs138619017 |
47126807 |
G |
allergy or anaphylactic reaction to food |
0.0014559 |
0.2117 |
0.003692 |
0.01803 |
genotyped |
1.38 |
rs138619017 |
47126807 |
G |
N41 Inflammatory diseases of prostate |
-0.0030614 |
0.18709 |
0.003692 |
0.01803 |
genotyped |
0.685 |
rs138619017 |
47126807 |
G |
N40 Hyperplasia of prostate |
0.00080159 |
0.8902 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
N43 Hydrocele and spermatocele |
0.0031472 |
0.14545 |
0.003692 |
0.01803 |
genotyped |
1.56 |
rs138619017 |
47126807 |
G |
N42 Other disorders of prostate |
0.0016506 |
0.44429 |
0.003692 |
0.01803 |
genotyped |
1.26 |
rs138619017 |
47126807 |
G |
N45 Orchitis and epididymitis |
0.0024287 |
0.15393 |
0.003692 |
0.01803 |
genotyped |
1.75 |
rs138619017 |
47126807 |
G |
N47 Redundant prepuce, phimosis and paraphimosis |
-0.00023293 |
0.93092 |
0.003692 |
0.01803 |
genotyped |
0.979 |
rs138619017 |
47126807 |
G |
heart arrhythmia |
-0.0023408 |
0.2673 |
0.003692 |
0.01803 |
genotyped |
0.856 |
rs138619017 |
47126807 |
G |
K80 Cholelithiasis |
0.00083681 |
0.78803 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
B95-B98 Bacterial, viral and other infectious agents |
-0.0067227 |
0.026465 |
0.003692 |
0.01803 |
genotyped |
0.802 |
rs138619017 |
47126807 |
G |
K82 Other diseases of gallbladder |
0.00045999 |
0.68694 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
K83 Other diseases of biliary tract |
0.00076532 |
0.5173 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
K85 Acute pancreatitis |
0.0001828 |
0.77748 |
0.003692 |
0.01803 |
genotyped |
1.14 |
rs138619017 |
47126807 |
G |
K86 Other diseases of pancreas |
0.00030714 |
0.73441 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
sarcoidosis |
-0.0010718 |
0.15797 |
0.003692 |
0.01803 |
genotyped |
0.571 |
rs138619017 |
47126807 |
G |
ankylosing spondylitis |
-0.00030403 |
0.73607 |
0.003692 |
0.01803 |
genotyped |
0.897 |
rs138619017 |
47126807 |
G |
K76 Other diseases of liver |
0.00045119 |
0.77447 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
viral infection |
-0.00083874 |
0.58252 |
0.003692 |
0.01803 |
genotyped |
0.897 |
rs138619017 |
47126807 |
G |
vasculitis |
0.0019998 |
0.031141 |
0.003692 |
0.01803 |
genotyped |
2.01 |
rs138619017 |
47126807 |
G |
cervical spondylosis |
0.0015416 |
0.29178 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
D41 Neoplasm of uncertain or unknown behaviour of urinary organs |
0.00092421 |
0.17491 |
0.003692 |
0.01803 |
genotyped |
1.83 |
rs138619017 |
47126807 |
G |
soft tissue inflammation |
0.00043938 |
0.53851 |
0.003692 |
0.01803 |
genotyped |
1.3 |
rs138619017 |
47126807 |
G |
A08 Viral and other specified intestinal infections |
0.00022199 |
0.77641 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
A09 Diarrhoea and gastro-enteritis of presumed infectious origin |
0.0023487 |
0.22126 |
0.003692 |
0.01803 |
genotyped |
1.21 |
rs138619017 |
47126807 |
G |
J20-J22 Other acute lower respiratory infections |
-0.00046474 |
0.84277 |
0.003692 |
0.01803 |
genotyped |
0.975 |
rs138619017 |
47126807 |
G |
essential hypertension |
-0.0021954 |
0.058175 |
0.003692 |
0.01803 |
genotyped |
0.61 |
rs138619017 |
47126807 |
G |
fracture head & neck |
0.0010033 |
0.27121 |
0.003692 |
0.01803 |
genotyped |
1.44 |
rs138619017 |
47126807 |
G |
A04 Other bacterial intestinal infections |
0.00050733 |
0.71244 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
anal problem |
-0.0010769 |
0.2744 |
0.003692 |
0.01803 |
genotyped |
0.716 |
rs138619017 |
47126807 |
G |
colitis/not crohns or ulcerative colitis |
0.0014159 |
0.10948 |
0.003692 |
0.01803 |
genotyped |
1.73 |
rs138619017 |
47126807 |
G |
ent disorder/not cancer |
9.0571e-05 |
0.9777 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
I08 Multiple valve diseases |
-0.0010778 |
0.32648 |
0.003692 |
0.01803 |
genotyped |
0.763 |
rs138619017 |
47126807 |
G |
K65-K67 Diseases of peritoneum |
-0.00015721 |
0.92421 |
0.003692 |
0.01803 |
genotyped |
0.983 |
rs138619017 |
47126807 |
G |
K55-K64 Other diseases of intestines |
-0.0025561 |
0.67751 |
0.003692 |
0.01803 |
genotyped |
0.981 |
rs138619017 |
47126807 |
G |
sciatica |
0.00010763 |
0.949 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
M51 Other intervertebral disk disorders |
-0.0034315 |
0.13119 |
0.003692 |
0.01803 |
genotyped |
0.82 |
rs138619017 |
47126807 |
G |
M50 Cervical disk disorders |
-0.00066882 |
0.52298 |
0.003692 |
0.01803 |
genotyped |
0.831 |
rs138619017 |
47126807 |
G |
M53 Other dorsopathies, not elsewhere classified |
0.00069102 |
0.27366 |
0.003692 |
0.01803 |
genotyped |
1.7 |
rs138619017 |
47126807 |
G |
duodenal ulcer |
0.00088701 |
0.42649 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
joint disorder |
0.0011486 |
0.83657 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
C34 Malignant neoplasm of bronchus and lung |
6.3727e-05 |
0.95166 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
H55-H59 Other disorders of eye and adnexa |
0.0015135 |
0.074295 |
0.003692 |
0.01803 |
genotyped |
1.9 |
rs138619017 |
47126807 |
G |
M07 Psoriatic and enteropathic arthropathies |
0.0001876 |
0.79401 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
bone disorder |
0.0032471 |
0.1983 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
H43-H45 Disorders of vitreous body and globe |
0.0004539 |
0.68421 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
H54 Blindness and low vision |
-0.00095824 |
0.22981 |
0.003692 |
0.01803 |
genotyped |
0.632 |
rs138619017 |
47126807 |
G |
haematology |
0.0028312 |
0.16462 |
0.003692 |
0.01803 |
genotyped |
1.23 |
rs138619017 |
47126807 |
G |
L80-L99 Other disorders of the skin and subcutaneous tissue |
3.2328e-05 |
0.99228 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
H50 Other strabismus |
-0.00052059 |
0.52594 |
0.003692 |
0.01803 |
genotyped |
0.791 |
rs138619017 |
47126807 |
G |
H52 Disorders of refraction and accommodation |
-0.00019807 |
0.86311 |
0.003692 |
0.01803 |
genotyped |
0.956 |
rs138619017 |
47126807 |
G |
H53 Visual disturbances |
-0.00092594 |
0.52948 |
0.003692 |
0.01803 |
genotyped |
0.878 |
rs138619017 |
47126807 |
G |
I30-I52 Other forms of heart disease |
-0.0024837 |
0.55876 |
0.003692 |
0.01803 |
genotyped |
0.962 |
rs138619017 |
47126807 |
G |
L08 Other local infections of skin and subcutaneous tissue |
0.00056075 |
0.55499 |
0.003692 |
0.01803 |
genotyped |
1.21 |
rs138619017 |
47126807 |
G |
H90-H95 Other disorders of ear |
0.0029399 |
0.10489 |
0.003692 |
0.01803 |
genotyped |
1.31 |
rs138619017 |
47126807 |
G |
L05 Pilonidal cyst |
-0.00034816 |
0.55984 |
0.003692 |
0.01803 |
genotyped |
0.744 |
rs138619017 |
47126807 |
G |
L03 Cellulitis |
-0.0014725 |
0.51445 |
0.003692 |
0.01803 |
genotyped |
0.917 |
rs138619017 |
47126807 |
G |
J90-J94 Other diseases of pleura |
0.00078502 |
0.71873 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
D70-D77 Other diseases of blood and blood-forming organs |
0.0046314 |
0.011466 |
0.003692 |
0.01803 |
genotyped |
1.52 |
rs138619017 |
47126807 |
G |
rheumatic fever |
-0.00056986 |
0.55062 |
0.003692 |
0.01803 |
genotyped |
0.827 |
rs138619017 |
47126807 |
G |
K81 Cholecystitis |
0.0011042 |
0.42786 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
liver/biliary/pancreas problem |
0.0029725 |
0.29606 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
J09-J18 Influenza and pneumonia |
0.0021058 |
0.4246 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
diabetic eye disease |
0.0015835 |
0.035522 |
0.003692 |
0.01803 |
genotyped |
2.32 |
rs138619017 |
47126807 |
G |
F00-F09 Organic, including symptomatic, mental disorders |
0.00020701 |
0.84682 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
tuberculosis (tb) |
-9.1005e-05 |
0.94037 |
0.003692 |
0.01803 |
genotyped |
0.982 |
rs138619017 |
47126807 |
G |
eye/eyelid problem |
0.0017253 |
0.60752 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
peripheral vascular disease |
-0.0016228 |
0.086479 |
0.003692 |
0.01803 |
genotyped |
0.577 |
rs138619017 |
47126807 |
G |
J84 Other interstitial pulmonary diseases |
0.00045748 |
0.59942 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
G40 Epilepsy |
0.0023153 |
0.15655 |
0.003692 |
0.01803 |
genotyped |
1.3 |
rs138619017 |
47126807 |
G |
G43 Migraine |
0.00031754 |
0.82204 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
G44 Other headache syndromes |
-0.001466 |
0.017685 |
0.003692 |
0.01803 |
genotyped |
0.311 |
rs138619017 |
47126807 |
G |
G45 Transient cerebral ischaemic attacks and related syndromes |
0.0001949 |
0.88592 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
G47 Sleep disorders |
-0.0014077 |
0.46861 |
0.003692 |
0.01803 |
genotyped |
0.895 |
rs138619017 |
47126807 |
G |
L40-L45 Papulosquamous disorders |
0.00080847 |
0.56965 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
E53 Deficiency of other B group vitamins |
0.00063037 |
0.38964 |
0.003692 |
0.01803 |
genotyped |
1.43 |
rs138619017 |
47126807 |
G |
B34 Viral infection of unspecified site |
-0.00027279 |
0.80834 |
0.003692 |
0.01803 |
genotyped |
0.936 |
rs138619017 |
47126807 |
G |
pancreatic disease |
0.00051264 |
0.53752 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
B37 Candidiasis |
-0.0010861 |
0.3858 |
0.003692 |
0.01803 |
genotyped |
0.811 |
rs138619017 |
47126807 |
G |
O48 Prolonged pregnancy |
-0.0022428 |
0.18569 |
0.003692 |
0.01803 |
genotyped |
0.655 |
rs138619017 |
47126807 |
G |
J35 Chronic diseases of tonsils and adenoids |
0.00091452 |
0.2853 |
0.003692 |
0.01803 |
genotyped |
1.46 |
rs138619017 |
47126807 |
G |
J30 Vasomotor and allergic rhinitis |
0.0013306 |
0.12522 |
0.003692 |
0.01803 |
genotyped |
1.71 |
rs138619017 |
47126807 |
G |
J31 Chronic rhinitis, nasopharyngitis and pharyngitis |
0.0015592 |
0.05048 |
0.003692 |
0.01803 |
genotyped |
2.11 |
rs138619017 |
47126807 |
G |
J32 Chronic sinusitis |
0.0023851 |
0.0745 |
0.003692 |
0.01803 |
genotyped |
1.5 |
rs138619017 |
47126807 |
G |
J33 Nasal polyp |
0.0028458 |
0.060261 |
0.003692 |
0.01803 |
genotyped |
1.44 |
rs138619017 |
47126807 |
G |
bowel problem |
-0.0030717 |
0.47228 |
0.003692 |
0.01803 |
genotyped |
0.952 |
rs138619017 |
47126807 |
G |
O42 Premature rupture of membranes |
-0.00059695 |
0.71027 |
0.003692 |
0.01803 |
genotyped |
0.882 |
rs138619017 |
47126807 |
G |
J38 Diseases of vocal cords and larynx, not elsewhere classified |
0.00097413 |
0.38724 |
0.003692 |
0.01803 |
genotyped |
1.26 |
rs138619017 |
47126807 |
G |
J39 Other diseases of upper respiratory tract |
0.00055931 |
0.43878 |
0.003692 |
0.01803 |
genotyped |
1.38 |
rs138619017 |
47126807 |
G |
O46 Antepartum haemorrhage, not elsewhere classified |
-0.00201 |
0.10796 |
0.003692 |
0.01803 |
genotyped |
0.494 |
rs138619017 |
47126807 |
G |
O47 False labour |
0.0020439 |
0.19929 |
0.003692 |
0.01803 |
genotyped |
1.55 |
rs138619017 |
47126807 |
G |
G50-G59 Nerve, nerve root and plexus disorders |
-0.00189 |
0.58575 |
0.003692 |
0.01803 |
genotyped |
0.955 |
rs138619017 |
47126807 |
G |
D06 Carcinoma in situ of cervix uteri |
0.0014084 |
0.5015 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
D05 Carcinoma in situ of breast |
-0.0020361 |
0.31493 |
0.003692 |
0.01803 |
genotyped |
0.761 |
rs138619017 |
47126807 |
G |
D04 Carcinoma in situ of skin |
-0.00052693 |
0.51737 |
0.003692 |
0.01803 |
genotyped |
0.786 |
rs138619017 |
47126807 |
G |
D03 Melanoma in situ |
0.00092376 |
0.24638 |
0.003692 |
0.01803 |
genotyped |
1.56 |
rs138619017 |
47126807 |
G |
I31 Other diseases of pericardium |
-0.00042314 |
0.63303 |
0.003692 |
0.01803 |
genotyped |
0.849 |
rs138619017 |
47126807 |
G |
I35 Nonrheumatic aortic valve disorders |
0.0010878 |
0.42264 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
I34 Nonrheumatic mitral valve disorders |
0.00081083 |
0.53369 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
hayfever/allergic rhinitis |
0.0024168 |
0.53478 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
A41 Other septicaemia |
0.003418 |
0.037917 |
0.003692 |
0.01803 |
genotyped |
1.47 |
rs138619017 |
47126807 |
G |
anaemia |
0.00085412 |
0.62387 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
E15-E16 Other disorders of glucose regulation and pancreatic internal secretion |
-0.00013598 |
0.86859 |
0.003692 |
0.01803 |
genotyped |
0.941 |
rs138619017 |
47126807 |
G |
F17 Mental and behavioural disorders due to use of tobacco |
-0.00050128 |
0.85708 |
0.003692 |
0.01803 |
genotyped |
0.981 |
rs138619017 |
47126807 |
G |
A49 Bacterial infection of unspecified site |
0.00026866 |
0.71688 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
N12 Tubulo-interstitial nephritis, not specified as acute or chronic |
0.0010199 |
0.21132 |
0.003692 |
0.01803 |
genotyped |
1.59 |
rs138619017 |
47126807 |
G |
N13 Obstructive and reflux uropathy |
8.6802e-06 |
0.99499 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
N17 Acute renal failure |
0.0012883 |
0.47421 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
irritable bowel syndrome |
-0.0034229 |
0.19151 |
0.003692 |
0.01803 |
genotyped |
0.862 |
rs138619017 |
47126807 |
G |
G30-G32 Other degenerative diseases of the nervous system |
-0.00054047 |
0.52347 |
0.003692 |
0.01803 |
genotyped |
0.795 |
rs138619017 |
47126807 |
G |
N18 Chronic renal failure |
-0.0020641 |
0.25011 |
0.003692 |
0.01803 |
genotyped |
0.825 |
rs138619017 |
47126807 |
G |
N19 Unspecified renal failure |
0.00093874 |
0.3515 |
0.003692 |
0.01803 |
genotyped |
1.32 |
rs138619017 |
47126807 |
G |
K70 Alcoholic liver disease |
0.00087264 |
0.26553 |
0.003692 |
0.01803 |
genotyped |
1.54 |
rs138619017 |
47126807 |
G |
K75 Other inflammatory liver diseases |
-0.00076558 |
0.27565 |
0.003692 |
0.01803 |
genotyped |
0.623 |
rs138619017 |
47126807 |
G |
K74 Fibrosis and cirrhosis of liver |
0.00018993 |
0.80663 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
I49 Other cardiac arrhythmias |
-0.0027896 |
0.042101 |
0.003692 |
0.01803 |
genotyped |
0.639 |
rs138619017 |
47126807 |
G |
I46 Cardiac arrest |
0.00019914 |
0.81074 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
I47 Paroxysmal tachycardia |
1.452e-05 |
0.99243 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
I44 Atrioventricular and left bundle-branch block |
-0.0017161 |
0.28777 |
0.003692 |
0.01803 |
genotyped |
0.82 |
rs138619017 |
47126807 |
G |
I45 Other conduction disorders |
-0.00045437 |
0.71847 |
0.003692 |
0.01803 |
genotyped |
0.917 |
rs138619017 |
47126807 |
G |
I42 Cardiomyopathy |
0.00031885 |
0.73904 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
M95-M99 Other disorders of the musculoskeletal system and connective tissue |
-0.00090198 |
0.26334 |
0.003692 |
0.01803 |
genotyped |
0.656 |
rs138619017 |
47126807 |
G |
H25 Senile cataract |
0.0018975 |
0.42884 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
H26 Other cataract |
0.0023031 |
0.4579 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
M65-M68 Disorders of synovium and tendon |
0.0032374 |
0.2055 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
O85-O92 Complications predominantly related to the puerperium |
0.0017788 |
0.14933 |
0.003692 |
0.01803 |
genotyped |
1.9 |
rs138619017 |
47126807 |
G |
N99 Postprocedural disorders of genito-urinary system, not elsewhere classified |
-0.00098623 |
0.28584 |
0.003692 |
0.01803 |
genotyped |
0.704 |
rs138619017 |
47126807 |
G |
G35-G37 Demyelinating diseases of the central nervous system |
-0.00030131 |
0.77117 |
0.003692 |
0.01803 |
genotyped |
0.92 |
rs138619017 |
47126807 |
G |
obstetric problem |
0.0017246 |
0.30135 |
0.003692 |
0.01803 |
genotyped |
1.41 |
rs138619017 |
47126807 |
G |
O00-O08 Pregnancy with abortive outcome |
0.0040719 |
0.16079 |
0.003692 |
0.01803 |
genotyped |
1.29 |
rs138619017 |
47126807 |
G |
back pain |
0.00095046 |
0.45134 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified |
0.0098178 |
0.048145 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
transient ischaemic attack (tia) |
0.00073013 |
0.49072 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
psoriasis |
-0.00012137 |
0.9465 |
0.003692 |
0.01803 |
genotyped |
0.989 |
rs138619017 |
47126807 |
G |
blistering/desquamating skin disorder |
-0.0021535 |
0.0037382 |
0.003692 |
0.01803 |
genotyped |
0.304 |
rs138619017 |
47126807 |
G |
abdominal hernia |
0.0018834 |
0.1492 |
0.003692 |
0.01803 |
genotyped |
1.39 |
rs138619017 |
47126807 |
G |
neck problem/injury |
0.0017482 |
0.2581 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
deep venous thrombosis (dvt) |
-0.001912 |
0.4268 |
0.003692 |
0.01803 |
genotyped |
0.907 |
rs138619017 |
47126807 |
G |
E00-E07 Disorders of thyroid gland |
-0.00052594 |
0.87402 |
0.003692 |
0.01803 |
genotyped |
0.987 |
rs138619017 |
47126807 |
G |
M80-M85 Disorders of bone density and structure |
0.0034338 |
0.1719 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
other urological problem (male) |
-0.0055767 |
0.27323 |
0.003692 |
0.01803 |
genotyped |
0.873 |
rs138619017 |
47126807 |
G |
I10-I15 Hypertensive diseases |
0.010889 |
0.072486 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
J00-J06 Acute upper respiratory infections |
0.0014525 |
0.32138 |
0.003692 |
0.01803 |
genotyped |
1.23 |
rs138619017 |
47126807 |
G |
M10 Gout |
-0.00029854 |
0.8437 |
0.003692 |
0.01803 |
genotyped |
0.962 |
rs138619017 |
47126807 |
G |
M13 Other arthritis |
0.0041683 |
0.14103 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
M15 Polyarthrosis |
-0.00023959 |
0.88731 |
0.003692 |
0.01803 |
genotyped |
0.975 |
rs138619017 |
47126807 |
G |
M17 Gonarthrosis [arthrosis of knee] |
0.00055332 |
0.87856 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
M16 Coxarthrosis [arthrosis of hip] |
0.0030065 |
0.28696 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
M19 Other arthrosis |
0.0019538 |
0.55931 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
M18 Arthrosis of first carpometacarpal joint |
0.00086364 |
0.37719 |
0.003692 |
0.01803 |
genotyped |
1.31 |
rs138619017 |
47126807 |
G |
stomach disorder |
-0.0055339 |
0.0023748 |
0.003692 |
0.01803 |
genotyped |
0.603 |
rs138619017 |
47126807 |
G |
osteoarthritis |
-0.0036217 |
0.43425 |
0.003692 |
0.01803 |
genotyped |
0.954 |
rs138619017 |
47126807 |
G |
L53 Other erythematous conditions |
0.0003876 |
0.53425 |
0.003692 |
0.01803 |
genotyped |
1.35 |
rs138619017 |
47126807 |
G |
L57 Skin changes due to chronic exposure to nonionising radiation |
0.00070872 |
0.58833 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
E11 Non-insulin-dependent diabetes mellitus |
0.0032524 |
0.33618 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
E10 Insulin-dependent diabetes mellitus |
0.0018603 |
0.18488 |
0.003692 |
0.01803 |
genotyped |
1.32 |
rs138619017 |
47126807 |
G |
J47 Bronchiectasis |
7.2031e-05 |
0.9508 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
E14 Unspecified diabetes mellitus |
0.0024736 |
0.05613 |
0.003692 |
0.01803 |
genotyped |
1.56 |
rs138619017 |
47126807 |
G |
J43 Emphysema |
8.8687e-05 |
0.93665 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
E16 Other disorders of pancreatic internal secretion |
-0.00013922 |
0.86529 |
0.003692 |
0.01803 |
genotyped |
0.939 |
rs138619017 |
47126807 |
G |
hepatitis |
0.0024293 |
0.047093 |
0.003692 |
0.01803 |
genotyped |
1.64 |
rs138619017 |
47126807 |
G |
hypertension |
0.0094553 |
0.15368 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
O04 Medical abortion |
0.0014112 |
0.38351 |
0.003692 |
0.01803 |
genotyped |
1.34 |
rs138619017 |
47126807 |
G |
O02 Other abnormal products of conception |
0.0014121 |
0.4227 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
O03 Spontaneous abortion |
0.0015117 |
0.40336 |
0.003692 |
0.01803 |
genotyped |
1.29 |
rs138619017 |
47126807 |
G |
G95 Other diseases of spinal cord |
-0.00015551 |
0.80918 |
0.003692 |
0.01803 |
genotyped |
0.892 |
rs138619017 |
47126807 |
G |
G93 Other disorders of brain |
-0.0013365 |
0.21215 |
0.003692 |
0.01803 |
genotyped |
0.701 |
rs138619017 |
47126807 |
G |
G91 Hydrocephalus |
0.00016767 |
0.77009 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
G99 Other disorders of nervous system in diseases classified elsewhere |
-0.00049434 |
0.5764 |
0.003692 |
0.01803 |
genotyped |
0.825 |
rs138619017 |
47126807 |
G |
K29 Gastritis and duodenitis |
-0.0039908 |
0.34722 |
0.003692 |
0.01803 |
genotyped |
0.937 |
rs138619017 |
47126807 |
G |
K22 Other diseases of oesophagus |
0.0021082 |
0.42146 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
K20 Oesophagitis |
-0.0003673 |
0.88544 |
0.003692 |
0.01803 |
genotyped |
0.983 |
rs138619017 |
47126807 |
G |
I26-I28 Pulmonary heart disease and diseases of pulmonary circulation |
-0.0018224 |
0.3048 |
0.003692 |
0.01803 |
genotyped |
0.841 |
rs138619017 |
47126807 |
G |
K26 Duodenal ulcer |
-0.0018642 |
0.21473 |
0.003692 |
0.01803 |
genotyped |
0.779 |
rs138619017 |
47126807 |
G |
muscle or soft tissue injuries |
0.0014549 |
0.32263 |
0.003692 |
0.01803 |
genotyped |
1.23 |
rs138619017 |
47126807 |
G |
other joint disorder |
0.0025327 |
0.13518 |
0.003692 |
0.01803 |
genotyped |
1.31 |
rs138619017 |
47126807 |
G |
K25 Gastric ulcer |
0.00093727 |
0.59436 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
E86 Volume depletion |
-0.00040212 |
0.77871 |
0.003692 |
0.01803 |
genotyped |
0.942 |
rs138619017 |
47126807 |
G |
E87 Other disorders of fluid, electrolyte and acid-base balance |
0.0011659 |
0.55003 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
E83 Disorders of mineral metabolism |
0.0016423 |
0.18399 |
0.003692 |
0.01803 |
genotyped |
1.38 |
rs138619017 |
47126807 |
G |
malabsorption/coeliac disease |
0.0010046 |
0.36911 |
0.003692 |
0.01803 |
genotyped |
1.26 |
rs138619017 |
47126807 |
G |
E89 Postprocedural endocrine and metabolic disorders, not elsewhere classified |
-0.00093012 |
0.34267 |
0.003692 |
0.01803 |
genotyped |
0.746 |
rs138619017 |
47126807 |
G |
N50 Other disorders of male genital organs |
-0.0044029 |
0.1576 |
0.003692 |
0.01803 |
genotyped |
0.739 |
rs138619017 |
47126807 |
G |
stroke |
0.00022786 |
0.91176 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
dermatology |
-0.00041996 |
0.90274 |
0.003692 |
0.01803 |
genotyped |
0.99 |
rs138619017 |
47126807 |
G |
head injury |
0.00027672 |
0.78169 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
I60-I69 Cerebrovascular diseases |
0.0026454 |
0.26894 |
0.003692 |
0.01803 |
genotyped |
1.15 |
rs138619017 |
47126807 |
G |
C50-C50 Malignant neoplasm of breast |
0.0061545 |
0.18371 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
heart attack/myocardial infarction |
0.0020433 |
0.41831 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
chronic obstructive airways disease/copd |
-0.00064857 |
0.52648 |
0.003692 |
0.01803 |
genotyped |
0.83 |
rs138619017 |
47126807 |
G |
M54 Dorsalgia |
-0.0055736 |
0.07614 |
0.003692 |
0.01803 |
genotyped |
0.847 |
rs138619017 |
47126807 |
G |
B35-B49 Mycoses |
-0.00078424 |
0.57331 |
0.003692 |
0.01803 |
genotyped |
0.885 |
rs138619017 |
47126807 |
G |
diverticular disease/diverticulitis |
-0.0024312 |
0.18145 |
0.003692 |
0.01803 |
genotyped |
0.804 |
rs138619017 |
47126807 |
G |
F20 Schizophrenia |
-0.00048067 |
0.44494 |
0.003692 |
0.01803 |
genotyped |
0.691 |
rs138619017 |
47126807 |
G |
C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue |
0.00035704 |
0.80194 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
D50 Iron deficiency anaemia |
0.0022988 |
0.32632 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
N99-N99 Other disorders of the genitourinary system |
-0.00098623 |
0.28584 |
0.003692 |
0.01803 |
genotyped |
0.704 |
rs138619017 |
47126807 |
G |
N25-N29 Other disorders of kidney and ureter |
0.0021154 |
0.12334 |
0.003692 |
0.01803 |
genotyped |
1.4 |
rs138619017 |
47126807 |
G |
K70-K77 Diseases of liver |
0.00097828 |
0.60691 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
peripheral nerve disorder |
-0.00040251 |
0.75345 |
0.003692 |
0.01803 |
genotyped |
0.928 |
rs138619017 |
47126807 |
G |
prostate problem (not cancer) |
-0.0067467 |
0.15664 |
0.003692 |
0.01803 |
genotyped |
0.83 |
rs138619017 |
47126807 |
G |
I77 Other disorders of arteries and arterioles |
0.00077597 |
0.44629 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
sleep apnoea |
-0.00047702 |
0.62887 |
0.003692 |
0.01803 |
genotyped |
0.862 |
rs138619017 |
47126807 |
G |
N28 Other disorders of kidney and ureter, not elsewhere classified |
0.0018842 |
0.15155 |
0.003692 |
0.01803 |
genotyped |
1.39 |
rs138619017 |
47126807 |
G |
I73 Other peripheral vascular diseases |
0.00050961 |
0.75424 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
I05-I09 Chronic rheumatic heart diseases |
-0.00064126 |
0.61192 |
0.003692 |
0.01803 |
genotyped |
0.885 |
rs138619017 |
47126807 |
G |
I71 Aortic aneurysm and dissection |
-0.00070124 |
0.47759 |
0.003692 |
0.01803 |
genotyped |
0.805 |
rs138619017 |
47126807 |
G |
I70 Atherosclerosis |
0.00056624 |
0.5533 |
0.003692 |
0.01803 |
genotyped |
1.21 |
rs138619017 |
47126807 |
G |
N23 Unspecified renal colic |
-0.0006167 |
0.59835 |
0.003692 |
0.01803 |
genotyped |
0.873 |
rs138619017 |
47126807 |
G |
N21 Calculus of lower urinary tract |
-0.00089397 |
0.23174 |
0.003692 |
0.01803 |
genotyped |
0.615 |
rs138619017 |
47126807 |
G |
N20 Calculus of kidney and ureter |
0.000902 |
0.62328 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
I78 Diseases of capillaries |
-0.00075154 |
0.28679 |
0.003692 |
0.01803 |
genotyped |
0.632 |
rs138619017 |
47126807 |
G |
C20 Malignant neoplasm of rectum |
0.0012851 |
0.15886 |
0.003692 |
0.01803 |
genotyped |
1.6 |
rs138619017 |
47126807 |
G |
E20-E35 Disorders of other endocrine glands |
-0.00011943 |
0.93016 |
0.003692 |
0.01803 |
genotyped |
0.981 |
rs138619017 |
47126807 |
G |
helicobacter pylori |
0.00019735 |
0.83186 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
M43 Other deforming dorsopathies |
-0.0012285 |
0.27168 |
0.003692 |
0.01803 |
genotyped |
0.742 |
rs138619017 |
47126807 |
G |
M41 Scoliosis |
0.00075416 |
0.38761 |
0.003692 |
0.01803 |
genotyped |
1.35 |
rs138619017 |
47126807 |
G |
M46 Other inflammatory spondylopathies |
-0.0004304 |
0.65424 |
0.003692 |
0.01803 |
genotyped |
0.868 |
rs138619017 |
47126807 |
G |
M47 Spondylosis |
-0.00092197 |
0.69014 |
0.003692 |
0.01803 |
genotyped |
0.95 |
rs138619017 |
47126807 |
G |
K51 Ulcerative colitis |
0.0011234 |
0.45645 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
allergy or anaphylactic reaction to drug |
0.0014871 |
0.35653 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
N35 Urethral stricture |
0.001701 |
0.26905 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
osteomyelitis |
-0.0011933 |
0.081697 |
0.003692 |
0.01803 |
genotyped |
0.461 |
rs138619017 |
47126807 |
G |
pulmonary embolism +/- dvt |
-0.00047451 |
0.76229 |
0.003692 |
0.01803 |
genotyped |
0.944 |
rs138619017 |
47126807 |
G |
F20-F29 Schizophrenia, schizotypal and delusional disorders |
-0.00063882 |
0.44883 |
0.003692 |
0.01803 |
genotyped |
0.761 |
rs138619017 |
47126807 |
G |
retinal problem |
0.0011025 |
0.4123 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
heart/cardiac problem |
-0.00017015 |
0.96851 |
0.003692 |
0.01803 |
genotyped |
0.997 |
rs138619017 |
47126807 |
G |
H61 Other disorders of external ear |
-0.0003408 |
0.68652 |
0.003692 |
0.01803 |
genotyped |
0.865 |
rs138619017 |
47126807 |
G |
H60 Otitis externa |
0.00037887 |
0.54369 |
0.003692 |
0.01803 |
genotyped |
1.35 |
rs138619017 |
47126807 |
G |
N40-N51 Diseases of male genital organs |
-0.0018805 |
0.80375 |
0.003692 |
0.01803 |
genotyped |
0.98 |
rs138619017 |
47126807 |
G |
H65 Nonsuppurative otitis media |
0.00069496 |
0.42648 |
0.003692 |
0.01803 |
genotyped |
1.32 |
rs138619017 |
47126807 |
G |
C43-C44 Melanoma and other malignant neoplasms of skin |
-0.0023899 |
0.46599 |
0.003692 |
0.01803 |
genotyped |
0.939 |
rs138619017 |
47126807 |
G |
H66 Suppurative and unspecified otitis media |
0.00011866 |
0.87545 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
C44 Other malignant neoplasms of skin |
-0.0037657 |
0.21739 |
0.003692 |
0.01803 |
genotyped |
0.892 |
rs138619017 |
47126807 |
G |
fracture pelvis & lower limb |
0.0026212 |
0.098534 |
0.003692 |
0.01803 |
genotyped |
1.37 |
rs138619017 |
47126807 |
G |
H83 Other diseases of inner ear |
-0.00013111 |
0.86597 |
0.003692 |
0.01803 |
genotyped |
0.936 |
rs138619017 |
47126807 |
G |
H81 Disorders of vestibular function |
-0.00092099 |
0.27776 |
0.003692 |
0.01803 |
genotyped |
0.677 |
rs138619017 |
47126807 |
G |
M86-M90 Other osteopathies |
-0.00034777 |
0.81761 |
0.003692 |
0.01803 |
genotyped |
0.955 |
rs138619017 |
47126807 |
G |
N60-N64 Disorders of breast |
0.0023252 |
0.23566 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
K40-K46 Hernia |
-0.0037341 |
0.48161 |
0.003692 |
0.01803 |
genotyped |
0.964 |
rs138619017 |
47126807 |
G |
L85 Other epidermal thickening |
0.00078308 |
0.26868 |
0.003692 |
0.01803 |
genotyped |
1.61 |
rs138619017 |
47126807 |
G |
L82 Seborrhoeic keratosis |
0.0016771 |
0.26228 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
L81 Other disorders of pigmentation |
0.00041231 |
0.58668 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
L89 Decubitus ulcer |
-0.00030136 |
0.65639 |
0.003692 |
0.01803 |
genotyped |
0.819 |
rs138619017 |
47126807 |
G |
C64-C68 Malignant neoplasms of urinary tract |
0.00070098 |
0.52625 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
M25 Other joint disorders, not elsewhere classified |
-0.0041902 |
0.16605 |
0.003692 |
0.01803 |
genotyped |
0.872 |
rs138619017 |
47126807 |
G |
fracture upper limb & shoulder |
0.0016655 |
0.30797 |
0.003692 |
0.01803 |
genotyped |
1.2 |
rs138619017 |
47126807 |
G |
J96 Respiratory failure, not elsewhere classified |
0.0013559 |
0.26414 |
0.003692 |
0.01803 |
genotyped |
1.32 |
rs138619017 |
47126807 |
G |
J92 Pleural plaque |
0.00093102 |
0.21033 |
0.003692 |
0.01803 |
genotyped |
1.67 |
rs138619017 |
47126807 |
G |
J93 Pneumothorax |
0.00025624 |
0.74349 |
0.003692 |
0.01803 |
genotyped |
1.14 |
rs138619017 |
47126807 |
G |
J90 Pleural effusion, not elsewhere classified |
0.00080599 |
0.67596 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
hyperthyroidism/thyrotoxicosis |
-0.00077085 |
0.6066 |
0.003692 |
0.01803 |
genotyped |
0.903 |
rs138619017 |
47126807 |
G |
J98 Other respiratory disorders |
-0.0025038 |
0.10086 |
0.003692 |
0.01803 |
genotyped |
0.721 |
rs138619017 |
47126807 |
G |
benign breast lump |
0.0025172 |
0.1361 |
0.003692 |
0.01803 |
genotyped |
1.62 |
rs138619017 |
47126807 |
G |
D60-D64 Aplastic and other anaemias |
-0.0043851 |
0.13888 |
0.003692 |
0.01803 |
genotyped |
0.861 |
rs138619017 |
47126807 |
G |
B07 Viral warts |
-0.00041157 |
0.56813 |
0.003692 |
0.01803 |
genotyped |
0.786 |
rs138619017 |
47126807 |
G |
E65-E68 Obesity and other hyperalimentation |
0.0011827 |
0.66385 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
D00-D09 In situ neoplasms |
-0.0002428 |
0.91014 |
0.003692 |
0.01803 |
genotyped |
0.984 |
rs138619017 |
47126807 |
G |
J40 Bronchitis, not specified as acute or chronic |
0.00090495 |
0.18289 |
0.003692 |
0.01803 |
genotyped |
1.82 |
rs138619017 |
47126807 |
G |
varicose veins |
-0.002867 |
0.0054902 |
0.003692 |
0.01803 |
genotyped |
0.448 |
rs138619017 |
47126807 |
G |
back problem |
-0.0048196 |
0.23421 |
0.003692 |
0.01803 |
genotyped |
0.917 |
rs138619017 |
47126807 |
G |
O75 Other complications of labour and delivery, not elsewhere classified |
0.00017341 |
0.89868 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
J03 Acute tonsillitis |
0.00047788 |
0.45761 |
0.003692 |
0.01803 |
genotyped |
1.42 |
rs138619017 |
47126807 |
G |
J02 Acute pharyngitis |
0.00056024 |
0.47812 |
0.003692 |
0.01803 |
genotyped |
1.32 |
rs138619017 |
47126807 |
G |
O70 Perineal laceration during delivery |
0.0029575 |
0.38576 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
O72 Postpartum haemorrhage |
0.00041998 |
0.81287 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
K13 Other diseases of lip and oral mucosa |
-0.00031721 |
0.82599 |
0.003692 |
0.01803 |
genotyped |
0.955 |
rs138619017 |
47126807 |
G |
K12 Stomatitis and related lesions |
-0.0010814 |
0.16137 |
0.003692 |
0.01803 |
genotyped |
0.575 |
rs138619017 |
47126807 |
G |
K11 Diseases of salivary glands |
-0.0003301 |
0.7009 |
0.003692 |
0.01803 |
genotyped |
0.873 |
rs138619017 |
47126807 |
G |
dyspepsia / indigestion |
-3.3052e-06 |
0.99572 |
0.003692 |
0.01803 |
genotyped |
0.997 |
rs138619017 |
47126807 |
G |
K14 Diseases of tongue |
-0.00037483 |
0.69054 |
0.003692 |
0.01803 |
genotyped |
0.88 |
rs138619017 |
47126807 |
G |
I20 Angina pectoris |
0.0061784 |
0.071547 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
I21 Acute myocardial infarction |
-0.0048623 |
0.038534 |
0.003692 |
0.01803 |
genotyped |
0.774 |
rs138619017 |
47126807 |
G |
I22 Subsequent myocardial infarction |
0.0010706 |
0.1396 |
0.003692 |
0.01803 |
genotyped |
1.85 |
rs138619017 |
47126807 |
G |
I24 Other acute ischaemic heart diseases |
-5.7691e-05 |
0.95408 |
0.003692 |
0.01803 |
genotyped |
0.983 |
rs138619017 |
47126807 |
G |
I25 Chronic ischaemic heart disease |
0.0018697 |
0.6347 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
I26 Pulmonary embolism |
-0.0031029 |
0.054297 |
0.003692 |
0.01803 |
genotyped |
0.699 |
rs138619017 |
47126807 |
G |
I27 Other pulmonary heart diseases |
0.0014206 |
0.068364 |
0.003692 |
0.01803 |
genotyped |
2.04 |
rs138619017 |
47126807 |
G |
C15-C26 Malignant neoplasms of digestive organs |
0.0031876 |
0.11099 |
0.003692 |
0.01803 |
genotyped |
1.27 |
rs138619017 |
47126807 |
G |
bladder problem (not cancer) |
-6.078e-05 |
0.97111 |
0.003692 |
0.01803 |
genotyped |
0.994 |
rs138619017 |
47126807 |
G |
M40-M43 Deforming dorsopathies |
-0.00066388 |
0.64123 |
0.003692 |
0.01803 |
genotyped |
0.906 |
rs138619017 |
47126807 |
G |
J30-J39 Other diseases of upper respiratory tract |
0.0083171 |
0.0087095 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
N64 Other disorders of breast |
-0.00061955 |
0.7195 |
0.003692 |
0.01803 |
genotyped |
0.891 |
rs138619017 |
47126807 |
G |
N63 Unspecified lump in breast |
0.0010622 |
0.3178 |
0.003692 |
0.01803 |
genotyped |
1.33 |
rs138619017 |
47126807 |
G |
N62 Hypertrophy of breast |
0.00050099 |
0.5174 |
0.003692 |
0.01803 |
genotyped |
1.29 |
rs138619017 |
47126807 |
G |
N60 Benign mammary dysplasia |
0.0012867 |
0.5365 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
renal/kidney failure |
-8.135e-05 |
0.90924 |
0.003692 |
0.01803 |
genotyped |
0.953 |
rs138619017 |
47126807 |
G |
K66 Other disorders of peritoneum |
-0.00027717 |
0.8537 |
0.003692 |
0.01803 |
genotyped |
0.963 |
rs138619017 |
47126807 |
G |
J45 Asthma |
0.0046003 |
0.25944 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
K62 Other diseases of anus and rectum |
-0.00097353 |
0.80686 |
0.003692 |
0.01803 |
genotyped |
0.982 |
rs138619017 |
47126807 |
G |
K63 Other diseases of intestine |
0.0011013 |
0.72671 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
K60 Fissure and fistula of anal and rectal regions |
0.00063722 |
0.67334 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
J44 Other chronic obstructive pulmonary disease |
0.0010947 |
0.64978 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
urinary frequency / incontinence |
0.00038622 |
0.70645 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
L60-L75 Disorders of skin appendages |
-0.00061474 |
0.81955 |
0.003692 |
0.01803 |
genotyped |
0.975 |
rs138619017 |
47126807 |
G |
spine arthritis/spondylitis |
-0.0016167 |
0.3184 |
0.003692 |
0.01803 |
genotyped |
0.83 |
rs138619017 |
47126807 |
G |
C67 Malignant neoplasm of bladder |
0.00063587 |
0.39572 |
0.003692 |
0.01803 |
genotyped |
1.41 |
rs138619017 |
47126807 |
G |
C64 Malignant neoplasm of kidney, except renal pelvis |
-0.0001215 |
0.87608 |
0.003692 |
0.01803 |
genotyped |
0.941 |
rs138619017 |
47126807 |
G |
rectal or colon adenoma/polyps |
0.00095567 |
0.31891 |
0.003692 |
0.01803 |
genotyped |
1.37 |
rs138619017 |
47126807 |
G |
C61 Malignant neoplasm of prostate |
0.0027232 |
0.53852 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
I95 Hypotension |
0.0019392 |
0.30318 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
E10-E14 Diabetes mellitus |
0.0043041 |
0.22023 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
substance abuse/dependency |
0.00021407 |
0.76205 |
0.003692 |
0.01803 |
genotyped |
1.14 |
rs138619017 |
47126807 |
G |
ovarian problem |
-0.0013305 |
0.66942 |
0.003692 |
0.01803 |
genotyped |
0.927 |
rs138619017 |
47126807 |
G |
bronchiectasis |
0.00025364 |
0.76237 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
M94 Other disorders of cartilage |
-0.0011551 |
0.11948 |
0.003692 |
0.01803 |
genotyped |
0.528 |
rs138619017 |
47126807 |
G |
bronchitis |
0.00022743 |
0.87862 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
F30-F39 Mood [affective] disorders |
-4.9197e-05 |
0.98674 |
0.003692 |
0.01803 |
genotyped |
0.998 |
rs138619017 |
47126807 |
G |
M15-M19 Arthrosis |
0.0011334 |
0.8247 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
eye trauma |
0.00014602 |
0.82213 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
H10-H13 Disorders of conjunctiva |
-0.00028961 |
0.73654 |
0.003692 |
0.01803 |
genotyped |
0.888 |
rs138619017 |
47126807 |
G |
M72 Fibroblastic disorders |
-2.616e-05 |
0.98739 |
0.003692 |
0.01803 |
genotyped |
0.997 |
rs138619017 |
47126807 |
G |
M71 Other bursopathies |
0.00014244 |
0.8534 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
M70 Soft tissue disorders related to use, overuse and pressure |
0.00062535 |
0.56466 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
M77 Other enthesopathies |
0.00032053 |
0.7747 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
M75 Shoulder lesions |
0.0004725 |
0.85196 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
migraine |
0.0016189 |
0.57228 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
M79 Other soft tissue disorders, not elsewhere classified |
-0.0047975 |
0.10231 |
0.003692 |
0.01803 |
genotyped |
0.847 |
rs138619017 |
47126807 |
G |
high cholesterol |
0.0010976 |
0.8349 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
osteoporosis |
0.0036541 |
0.089661 |
0.003692 |
0.01803 |
genotyped |
1.26 |
rs138619017 |
47126807 |
G |
fracture |
0.0036596 |
0.11093 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
C18 Malignant neoplasm of colon |
0.001873 |
0.15202 |
0.003692 |
0.01803 |
genotyped |
1.39 |
rs138619017 |
47126807 |
G |
F40-F48 Neurotic, stress-related and somatoform disorders |
0.00074941 |
0.7434 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
G90-G99 Other disorders of the nervous system |
-0.0019659 |
0.25287 |
0.003692 |
0.01803 |
genotyped |
0.818 |
rs138619017 |
47126807 |
G |
ear/vestibular disorder |
-0.00049444 |
0.81483 |
0.003692 |
0.01803 |
genotyped |
0.967 |
rs138619017 |
47126807 |
G |
oesophagitis/barretts oesophagus |
0.00063295 |
0.511 |
0.003692 |
0.01803 |
genotyped |
1.23 |
rs138619017 |
47126807 |
G |
tropical & travel-related infections |
-0.00024106 |
0.70571 |
0.003692 |
0.01803 |
genotyped |
0.835 |
rs138619017 |
47126807 |
G |
M06 Other rheumatoid arthritis |
-0.00051296 |
0.76993 |
0.003692 |
0.01803 |
genotyped |
0.952 |
rs138619017 |
47126807 |
G |
H33 Retinal detachments and breaks |
0.0032159 |
0.034395 |
0.003692 |
0.01803 |
genotyped |
1.51 |
rs138619017 |
47126807 |
G |
M05 Seropositive rheumatoid arthritis |
0.0011313 |
0.081495 |
0.003692 |
0.01803 |
genotyped |
2.24 |
rs138619017 |
47126807 |
G |
H36 Retinal disorders in diseases classified elsewhere |
0.00079187 |
0.41815 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
H34 Retinal vascular occlusions |
8.0848e-05 |
0.89615 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
H35 Other retinal disorders |
0.0020631 |
0.19253 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
G31 Other degenerative diseases of nervous system, not elsewhere classified |
-0.000588 |
0.37741 |
0.003692 |
0.01803 |
genotyped |
0.668 |
rs138619017 |
47126807 |
G |
G35 Multiple sclerosis |
-0.00050929 |
0.59665 |
0.003692 |
0.01803 |
genotyped |
0.848 |
rs138619017 |
47126807 |
G |
L60 Nail disorders |
-0.0011507 |
0.20987 |
0.003692 |
0.01803 |
genotyped |
0.66 |
rs138619017 |
47126807 |
G |
E04 Other non-toxic goitre |
-0.0020329 |
0.064447 |
0.003692 |
0.01803 |
genotyped |
0.603 |
rs138619017 |
47126807 |
G |
H40-H42 Glaucoma |
0.00056996 |
0.7476 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
E03 Other hypothyroidism |
0.0032004 |
0.29143 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
L02 Cutaneous abscess, furuncle and carbuncle |
0.0017525 |
0.17834 |
0.003692 |
0.01803 |
genotyped |
1.37 |
rs138619017 |
47126807 |
G |
connective tissue disorder |
0.004155 |
0.0030314 |
0.003692 |
0.01803 |
genotyped |
1.89 |
rs138619017 |
47126807 |
G |
K80-K87 Disorders of gallbladder, biliary tract and pancreas |
0.0023245 |
0.50367 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
gall bladder disease |
0.0014831 |
0.51536 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
L50-L54 Urticaria and erythema |
-0.00018034 |
0.83621 |
0.003692 |
0.01803 |
genotyped |
0.93 |
rs138619017 |
47126807 |
G |
C83 Diffuse non-Hodgkin's lymphoma |
0.00086695 |
0.20099 |
0.003692 |
0.01803 |
genotyped |
1.77 |
rs138619017 |
47126807 |
G |
G80-G83 Cerebral palsy and other paralytic syndromes |
-0.00029296 |
0.81419 |
0.003692 |
0.01803 |
genotyped |
0.944 |
rs138619017 |
47126807 |
G |
O32 Maternal care for known or suspected malpresentation of foetus |
0.0021501 |
0.18395 |
0.003692 |
0.01803 |
genotyped |
1.56 |
rs138619017 |
47126807 |
G |
O34 Maternal care for known or suspected abnormality of pelvic organs |
0.0024437 |
0.19837 |
0.003692 |
0.01803 |
genotyped |
1.44 |
rs138619017 |
47126807 |
G |
O36 Maternal care for other known or suspected foetal problems |
0.0025876 |
0.2188 |
0.003692 |
0.01803 |
genotyped |
1.37 |
rs138619017 |
47126807 |
G |
C30-C39 Malignant neoplasms of respiratory and intrathoracic organs |
0.00071017 |
0.53229 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
G81 Hemiplegia |
-6.6559e-05 |
0.94868 |
0.003692 |
0.01803 |
genotyped |
0.981 |
rs138619017 |
47126807 |
G |
H65-H75 Diseases of middle ear and mastoid |
0.001506 |
0.32358 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
J06 Acute upper respiratory infections of multiple and unspecified sites |
0.00082158 |
0.29057 |
0.003692 |
0.01803 |
genotyped |
1.51 |
rs138619017 |
47126807 |
G |
D80-D89 Certain disorders involving the immune mechanism |
0.00012726 |
0.88426 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
K50-K52 Noninfective enteritis and colitis |
0.00441 |
0.22387 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
K59 Other functional intestinal disorders |
-0.0012619 |
0.65341 |
0.003692 |
0.01803 |
genotyped |
0.953 |
rs138619017 |
47126807 |
G |
K58 Irritable bowel syndrome |
-0.00088104 |
0.65768 |
0.003692 |
0.01803 |
genotyped |
0.935 |
rs138619017 |
47126807 |
G |
K57 Diverticular disease of intestine |
0.0019352 |
0.6402 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
K56 Paralytic ileus and intestinal obstruction without hernia |
0.0016213 |
0.33695 |
0.003692 |
0.01803 |
genotyped |
1.19 |
rs138619017 |
47126807 |
G |
K55 Vascular disorders of intestine |
0.00011718 |
0.89236 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
K52 Other non-infective gastro-enteritis and colitis |
0.0045807 |
0.17184 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
J60-J70 Lung diseases due to external agents |
0.0017579 |
0.036858 |
0.003692 |
0.01803 |
genotyped |
2.12 |
rs138619017 |
47126807 |
G |
K50 Crohn's disease [regional enteritis] |
-0.00039471 |
0.72303 |
0.003692 |
0.01803 |
genotyped |
0.909 |
rs138619017 |
47126807 |
G |
E78 Disorders of lipoprotein metabolism and other lipidaemias |
0.0062692 |
0.17524 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
thyroid problem (not cancer) |
0.0030938 |
0.41608 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
G70-G73 Diseases of myoneural junction and muscle |
0.00069045 |
0.26371 |
0.003692 |
0.01803 |
genotyped |
1.73 |
rs138619017 |
47126807 |
G |
fibromyalgia |
-0.0007255 |
0.2728 |
0.003692 |
0.01803 |
genotyped |
0.606 |
rs138619017 |
47126807 |
G |
neurology |
0.0002568 |
0.95264 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
diabetes |
0.0046106 |
0.18328 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
N10-N16 Renal tubulo-interstitial diseases |
0.0012606 |
0.44498 |
0.003692 |
0.01803 |
genotyped |
1.15 |
rs138619017 |
47126807 |
G |
respiratory infection |
0.00029328 |
0.88791 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
cervical problem |
0.001694 |
0.30645 |
0.003692 |
0.01803 |
genotyped |
1.4 |
rs138619017 |
47126807 |
G |
venous thromboembolic disease |
-0.0023267 |
0.39057 |
0.003692 |
0.01803 |
genotyped |
0.911 |
rs138619017 |
47126807 |
G |
N85 Other noninflammatory disorders of uterus, except cervix |
-0.0036151 |
0.30649 |
0.003692 |
0.01803 |
genotyped |
0.853 |
rs138619017 |
47126807 |
G |
N84 Polyp of female genital tract |
0.0053727 |
0.28141 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
N87 Dysplasia of cervix uteri |
-0.0020361 |
0.29251 |
0.003692 |
0.01803 |
genotyped |
0.741 |
rs138619017 |
47126807 |
G |
N86 Erosion and ectropion of cervix uteri |
0.0014492 |
0.33232 |
0.003692 |
0.01803 |
genotyped |
1.43 |
rs138619017 |
47126807 |
G |
N81 Female genital prolapse |
-0.0025297 |
0.61516 |
0.003692 |
0.01803 |
genotyped |
0.95 |
rs138619017 |
47126807 |
G |
N80 Endometriosis |
-0.0067531 |
0.026339 |
0.003692 |
0.01803 |
genotyped |
0.672 |
rs138619017 |
47126807 |
G |
N83 Noninflammatory disorders of ovary, Fallopian tube and broad ligament |
0.00291 |
0.40698 |
0.003692 |
0.01803 |
genotyped |
1.14 |
rs138619017 |
47126807 |
G |
clotting disorder/excessive bleeding |
0.00074041 |
0.33682 |
0.003692 |
0.01803 |
genotyped |
1.46 |
rs138619017 |
47126807 |
G |
rosacea |
-0.00024185 |
0.72646 |
0.003692 |
0.01803 |
genotyped |
0.858 |
rs138619017 |
47126807 |
G |
N89 Other noninflammatory disorders of vagina |
4.2472e-06 |
0.99827 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
N88 Other noninflammatory disorders of cervix uteri |
0.0016776 |
0.42228 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
H53-H54 Visual disturbances and blindness |
-0.0017413 |
0.29253 |
0.003692 |
0.01803 |
genotyped |
0.825 |
rs138619017 |
47126807 |
G |
F31 Bipolar affective disorder |
-0.0015678 |
0.063061 |
0.003692 |
0.01803 |
genotyped |
0.514 |
rs138619017 |
47126807 |
G |
F32 Depressive episode |
0.00061628 |
0.82873 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
F33 Recurrent depressive disorder |
-6.7275e-05 |
0.92646 |
0.003692 |
0.01803 |
genotyped |
0.962 |
rs138619017 |
47126807 |
G |
D69 Purpura and other haemorrhagic conditions |
-0.00085278 |
0.43786 |
0.003692 |
0.01803 |
genotyped |
0.807 |
rs138619017 |
47126807 |
G |
D68 Other coagulation defects |
0.00012237 |
0.88171 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
D64 Other anaemias |
-0.003294 |
0.24876 |
0.003692 |
0.01803 |
genotyped |
0.886 |
rs138619017 |
47126807 |
G |
miscarriage |
0.0014901 |
0.29848 |
0.003692 |
0.01803 |
genotyped |
1.49 |
rs138619017 |
47126807 |
G |
D63 Anaemia in chronic diseases classified elsewhere |
-0.00039402 |
0.58233 |
0.003692 |
0.01803 |
genotyped |
0.791 |
rs138619017 |
47126807 |
G |
N00-N08 Glomerular diseases |
0.00060146 |
0.62645 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
varicella zoster virus |
0.00027972 |
0.81198 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
I64 Stroke, not specified as haemorrhage or infarction |
-0.000432 |
0.62282 |
0.003692 |
0.01803 |
genotyped |
0.844 |
rs138619017 |
47126807 |
G |
N39 Other disorders of urinary system |
-0.00099414 |
0.78372 |
0.003692 |
0.01803 |
genotyped |
0.978 |
rs138619017 |
47126807 |
G |
emphysema/chronic bronchitis |
-0.00085072 |
0.73412 |
0.003692 |
0.01803 |
genotyped |
0.96 |
rs138619017 |
47126807 |
G |
I67 Other cerebrovascular diseases |
0.0023339 |
0.076378 |
0.003692 |
0.01803 |
genotyped |
1.5 |
rs138619017 |
47126807 |
G |
B00-B09 Viral infections characterized by skin and mucous membrane lesions |
-0.0012411 |
0.25207 |
0.003692 |
0.01803 |
genotyped |
0.725 |
rs138619017 |
47126807 |
G |
I61 Intracerebral haemorrhage |
0.00021171 |
0.76874 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
I63 Cerebral infarction |
0.0026117 |
0.086298 |
0.003692 |
0.01803 |
genotyped |
1.4 |
rs138619017 |
47126807 |
G |
N30 Cystitis |
-0.00037371 |
0.7982 |
0.003692 |
0.01803 |
genotyped |
0.948 |
rs138619017 |
47126807 |
G |
N31 Neuromuscular dysfunction of bladder, not elsewhere classified |
0.0001664 |
0.87777 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
N32 Other disorders of bladder |
-0.0004635 |
0.85177 |
0.003692 |
0.01803 |
genotyped |
0.978 |
rs138619017 |
47126807 |
G |
O80-O84 Delivery |
-0.00084216 |
0.73718 |
0.003692 |
0.01803 |
genotyped |
0.932 |
rs138619017 |
47126807 |
G |
N36 Other disorders of urethra |
-0.00028104 |
0.70759 |
0.003692 |
0.01803 |
genotyped |
0.859 |
rs138619017 |
47126807 |
G |
C56 Malignant neoplasm of ovary |
-0.00040839 |
0.76717 |
0.003692 |
0.01803 |
genotyped |
0.888 |
rs138619017 |
47126807 |
G |
C54 Malignant neoplasm of corpus uteri |
-0.00077812 |
0.64743 |
0.003692 |
0.01803 |
genotyped |
0.862 |
rs138619017 |
47126807 |
G |
asthma |
-0.012506 |
0.016734 |
0.003692 |
0.01803 |
genotyped |
0.885 |
rs138619017 |
47126807 |
G |
N20-N23 Urolithiasis |
6.9663e-05 |
0.97389 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
C50 Malignant neoplasm of breast |
0.0061545 |
0.18371 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
H02 Other disorders of eyelid |
-0.0012367 |
0.54221 |
0.003692 |
0.01803 |
genotyped |
0.913 |
rs138619017 |
47126807 |
G |
H01 Other inflammation of eyelid |
-0.0016323 |
0.012955 |
0.003692 |
0.01803 |
genotyped |
0.316 |
rs138619017 |
47126807 |
G |
H00 Hordeolum and chalazion |
0.00086935 |
0.45397 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
M31 Other necrotising vasculopathies |
-0.00039957 |
0.53973 |
0.003692 |
0.01803 |
genotyped |
0.751 |
rs138619017 |
47126807 |
G |
H04 Disorders of lachrymal system |
-0.00045855 |
0.71765 |
0.003692 |
0.01803 |
genotyped |
0.917 |
rs138619017 |
47126807 |
G |
cataract |
0.00031572 |
0.87504 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
M00-M03 Infectious arthropathies |
0.00025635 |
0.66596 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems |
0.0062349 |
0.092804 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
N80-N98 Noninflammatory disorders of female genital tract |
-0.00011151 |
0.99058 |
0.003692 |
0.01803 |
genotyped |
0.999 |
rs138619017 |
47126807 |
G |
breast cysts |
-0.0016928 |
0.39098 |
0.003692 |
0.01803 |
genotyped |
0.786 |
rs138619017 |
47126807 |
G |
I65 Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction |
-0.00082917 |
0.33528 |
0.003692 |
0.01803 |
genotyped |
0.712 |
rs138619017 |
47126807 |
G |
L40 Psoriasis |
0.00089668 |
0.47668 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
muscle/soft tissue problem |
-0.00016335 |
0.94735 |
0.003692 |
0.01803 |
genotyped |
0.992 |
rs138619017 |
47126807 |
G |
uterine problem |
0.0015525 |
0.77155 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
rheumatoid arthritis |
0.0013662 |
0.45154 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
I60 Subarachnoid haemorrhage |
0.00016067 |
0.83492 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
H72 Perforation of tympanic membrane |
-0.00030732 |
0.7167 |
0.003692 |
0.01803 |
genotyped |
0.878 |
rs138619017 |
47126807 |
G |
M45-M49 Spondylopathies |
2.0084e-05 |
0.99437 |
0.003692 |
0.01803 |
genotyped |
1 |
rs138619017 |
47126807 |
G |
C00-C14 Malignant neoplasms of lip, oral cavity and pharynx |
-0.00092236 |
0.20695 |
0.003692 |
0.01803 |
genotyped |
0.591 |
rs138619017 |
47126807 |
G |
C51-C58 Malignant neoplasms of female genital organs |
-0.0031247 |
0.19499 |
0.003692 |
0.01803 |
genotyped |
0.743 |
rs138619017 |
47126807 |
G |
K21 Gastro-oesophageal reflux disease |
-0.0034058 |
0.38566 |
0.003692 |
0.01803 |
genotyped |
0.938 |
rs138619017 |
47126807 |
G |
spinal injury |
0.00029245 |
0.66825 |
0.003692 |
0.01803 |
genotyped |
1.21 |
rs138619017 |
47126807 |
G |
throat or larynx disorder |
0.001218 |
0.43698 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
peritonitis |
0.00010164 |
0.91976 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
H90 Conductive and sensorineural hearing loss |
0.00075811 |
0.3652 |
0.003692 |
0.01803 |
genotyped |
1.39 |
rs138619017 |
47126807 |
G |
H91 Other hearing loss |
0.00086798 |
0.5446 |
0.003692 |
0.01803 |
genotyped |
1.14 |
rs138619017 |
47126807 |
G |
H92 Otalgia and effusion of ear |
0.00071399 |
0.25148 |
0.003692 |
0.01803 |
genotyped |
1.75 |
rs138619017 |
47126807 |
G |
H93 Other disorders of ear, not elsewhere classified |
0.00066827 |
0.32517 |
0.003692 |
0.01803 |
genotyped |
1.55 |
rs138619017 |
47126807 |
G |
J80-J84 Other respiratory diseases principally affecting the interstitium |
-0.00078251 |
0.47657 |
0.003692 |
0.01803 |
genotyped |
0.822 |
rs138619017 |
47126807 |
G |
osteopenia |
0.0012937 |
0.13314 |
0.003692 |
0.01803 |
genotyped |
1.69 |
rs138619017 |
47126807 |
G |
I95-I99 Other and unspecified disorders of the circulatory system |
0.0018347 |
0.35581 |
0.003692 |
0.01803 |
genotyped |
1.15 |
rs138619017 |
47126807 |
G |
nasal/sinus disorder |
-0.0016682 |
0.41594 |
0.003692 |
0.01803 |
genotyped |
0.887 |
rs138619017 |
47126807 |
G |
L97 Ulcer of lower limb, not elsewhere classified |
-0.00047897 |
0.58464 |
0.003692 |
0.01803 |
genotyped |
0.827 |
rs138619017 |
47126807 |
G |
L90 Atrophic disorders of skin |
-0.0016511 |
0.24852 |
0.003692 |
0.01803 |
genotyped |
0.783 |
rs138619017 |
47126807 |
G |
L91 Hypertrophic disorders of skin |
0.00027671 |
0.75782 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
L92 Granulomatous disorders of skin and subcutaneous tissue |
0.0008267 |
0.20521 |
0.003692 |
0.01803 |
genotyped |
1.81 |
rs138619017 |
47126807 |
G |
L98 Other disorders of skin and subcutaneous tissue, not elsewhere classified |
-0.0026389 |
0.18589 |
0.003692 |
0.01803 |
genotyped |
0.818 |
rs138619017 |
47126807 |
G |
N17-N19 Renal failure |
0.00012348 |
0.95984 |
0.003692 |
0.01803 |
genotyped |
1.01 |
rs138619017 |
47126807 |
G |
inflammatory bowel disease |
0.00099815 |
0.52924 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
M20-M25 Other joint disorders |
0.0014764 |
0.76619 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
E70-E90 Metabolic disorders |
0.0082319 |
0.10466 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
J69 Pneumonitis due to solids and liquids |
0.0011469 |
0.082643 |
0.003692 |
0.01803 |
genotyped |
2.22 |
rs138619017 |
47126807 |
G |
O99 Other maternal diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium |
0.00281 |
0.16514 |
0.003692 |
0.01803 |
genotyped |
1.45 |
rs138619017 |
47126807 |
G |
disorder or pituitary gland |
0.00015855 |
0.8073 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
G62 Other polyneuropathies |
8.024e-05 |
0.93068 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
dry eyes |
-0.00036979 |
0.57532 |
0.003692 |
0.01803 |
genotyped |
0.773 |
rs138619017 |
47126807 |
G |
O63 Long labour |
-0.0021491 |
0.31634 |
0.003692 |
0.01803 |
genotyped |
0.78 |
rs138619017 |
47126807 |
G |
other venous/lymphatic disease |
-0.0029237 |
0.0084619 |
0.003692 |
0.01803 |
genotyped |
0.493 |
rs138619017 |
47126807 |
G |
O68 Labour and delivery complicated by foetal stress [distress] |
-0.0013488 |
0.62547 |
0.003692 |
0.01803 |
genotyped |
0.912 |
rs138619017 |
47126807 |
G |
O69 Labour and delivery complicated by umbilical cord complications |
-0.0013267 |
0.2825 |
0.003692 |
0.01803 |
genotyped |
0.62 |
rs138619017 |
47126807 |
G |
K65 Peritonitis |
0.00048504 |
0.52854 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
J18 Pneumonia, organism unspecified |
0.0017802 |
0.47989 |
0.003692 |
0.01803 |
genotyped |
1.09 |
rs138619017 |
47126807 |
G |
L29 Pruritus |
0.00094152 |
0.20608 |
0.003692 |
0.01803 |
genotyped |
1.68 |
rs138619017 |
47126807 |
G |
M35 Other systemic involvement of connective tissue |
0.0014021 |
0.23124 |
0.003692 |
0.01803 |
genotyped |
1.36 |
rs138619017 |
47126807 |
G |
F10-F19 Mental and behavioural disorders due to psychoactive substance use |
0.0011338 |
0.72561 |
0.003692 |
0.01803 |
genotyped |
1.03 |
rs138619017 |
47126807 |
G |
K01 Embedded and impacted teeth |
-0.00012221 |
0.91691 |
0.003692 |
0.01803 |
genotyped |
0.973 |
rs138619017 |
47126807 |
G |
K02 Dental caries |
-0.0010883 |
0.46788 |
0.003692 |
0.01803 |
genotyped |
0.863 |
rs138619017 |
47126807 |
G |
K04 Diseases of pulp and periapical tissues |
-0.00042483 |
0.74378 |
0.003692 |
0.01803 |
genotyped |
0.926 |
rs138619017 |
47126807 |
G |
K05 Gingivitis and periodontal diseases |
0.00018438 |
0.8122 |
0.003692 |
0.01803 |
genotyped |
1.1 |
rs138619017 |
47126807 |
G |
K07 Dentofacial anomalies [including malocclusion] |
0.0011308 |
0.08726 |
0.003692 |
0.01803 |
genotyped |
2.2 |
rs138619017 |
47126807 |
G |
K08 Other disorders of teeth and supporting structures |
0.00067781 |
0.625 |
0.003692 |
0.01803 |
genotyped |
1.11 |
rs138619017 |
47126807 |
G |
K61 Abscess of anal and rectal regions |
0.00018856 |
0.84945 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
I10 Essential (primary) hypertension |
0.010914 |
0.071527 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
I12 Hypertensive renal disease |
-0.00049385 |
0.63922 |
0.003692 |
0.01803 |
genotyped |
0.874 |
rs138619017 |
47126807 |
G |
G60-G64 Polyneuropathies and other disorders of the peripheral nervous system |
0.00068535 |
0.54684 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
N75 Diseases of Bartholin's gland |
0.0010037 |
0.45146 |
0.003692 |
0.01803 |
genotyped |
1.37 |
rs138619017 |
47126807 |
G |
N76 Other inflammation of vagina and vulva |
0.0018754 |
0.17333 |
0.003692 |
0.01803 |
genotyped |
1.73 |
rs138619017 |
47126807 |
G |
N70 Salpingitis and oophoritis |
-0.001001 |
0.37908 |
0.003692 |
0.01803 |
genotyped |
0.651 |
rs138619017 |
47126807 |
G |
N72 Inflammatory disease of cervix uteri |
0.00028672 |
0.86515 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
N73 Other female pelvic inflammatory diseases |
0.0019901 |
0.44275 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
I70-I79 Diseases of arteries, arterioles and capillaries |
0.0006932 |
0.76321 |
0.003692 |
0.01803 |
genotyped |
1.04 |
rs138619017 |
47126807 |
G |
infection of nervous system |
-0.00035509 |
0.77363 |
0.003692 |
0.01803 |
genotyped |
0.931 |
rs138619017 |
47126807 |
G |
cranial nerve problem/palsy |
-0.0013477 |
0.080381 |
0.003692 |
0.01803 |
genotyped |
0.501 |
rs138619017 |
47126807 |
G |
K92 Other diseases of digestive system |
-0.00090293 |
0.72547 |
0.003692 |
0.01803 |
genotyped |
0.96 |
rs138619017 |
47126807 |
G |
K91 Postprocedural disorders of digestive system, not elsewhere classified |
0.00081017 |
0.44941 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
K90 Intestinal malabsorption |
0.00026717 |
0.82587 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
L55-L59 Radiation-related disorders of the skin and subcutaneous tissue |
0.00069658 |
0.60372 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
arthritis (nos) |
-3.5095e-05 |
0.98136 |
0.003692 |
0.01803 |
genotyped |
0.995 |
rs138619017 |
47126807 |
G |
chronic fatigue syndrome |
0.00022241 |
0.84789 |
0.003692 |
0.01803 |
genotyped |
1.05 |
rs138619017 |
47126807 |
G |
H60-H62 Diseases of external ear |
-0.00010876 |
0.9157 |
0.003692 |
0.01803 |
genotyped |
0.969 |
rs138619017 |
47126807 |
G |
H30-H36 Disorders of choroid and retina |
0.0048509 |
0.034039 |
0.003692 |
0.01803 |
genotyped |
1.32 |
rs138619017 |
47126807 |
G |
I89 Other non-infective disorders of lymphatic vessels and lymph nodes |
0.00038611 |
0.5776 |
0.003692 |
0.01803 |
genotyped |
1.28 |
rs138619017 |
47126807 |
G |
K35-K38 Diseases of appendix |
0.00016625 |
0.9178 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
I83 Varicose veins of lower extremities |
0.0038141 |
0.16131 |
0.003692 |
0.01803 |
genotyped |
1.16 |
rs138619017 |
47126807 |
G |
I80 Phlebitis and thrombophlebitis |
-0.00067658 |
0.68241 |
0.003692 |
0.01803 |
genotyped |
0.929 |
rs138619017 |
47126807 |
G |
pneumonia |
0.00033779 |
0.86976 |
0.003692 |
0.01803 |
genotyped |
1.02 |
rs138619017 |
47126807 |
G |
I20-I25 Ischaemic heart diseases |
0.0049988 |
0.24251 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
I84 Haemorrhoids |
0.006326 |
0.11152 |
0.003692 |
0.01803 |
genotyped |
1.12 |
rs138619017 |
47126807 |
G |
I85 Oesophageal varices |
0.00098975 |
0.10757 |
0.003692 |
0.01803 |
genotyped |
2.21 |
rs138619017 |
47126807 |
G |
psoriatic arthropathy |
0.00042657 |
0.57681 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
M89 Other disorders of bone |
-0.0010953 |
0.30012 |
0.003692 |
0.01803 |
genotyped |
0.742 |
rs138619017 |
47126807 |
G |
M86 Osteomyelitis |
-0.00086229 |
0.16378 |
0.003692 |
0.01803 |
genotyped |
0.504 |
rs138619017 |
47126807 |
G |
M87 Osteonecrosis |
0.00072519 |
0.25506 |
0.003692 |
0.01803 |
genotyped |
1.72 |
rs138619017 |
47126807 |
G |
M84 Disorders of continuity of bone |
0.00060319 |
0.56391 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
M85 Other disorders of bone density and structure |
-0.00099975 |
0.26149 |
0.003692 |
0.01803 |
genotyped |
0.681 |
rs138619017 |
47126807 |
G |
M80 Osteoporosis with pathological fracture |
0.0014623 |
0.070368 |
0.003692 |
0.01803 |
genotyped |
1.97 |
rs138619017 |
47126807 |
G |
M81 Osteoporosis without pathological fracture |
0.0023557 |
0.25262 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
anxiety/panic attacks |
-0.0074166 |
0.00025271 |
0.003692 |
0.01803 |
genotyped |
0.581 |
rs138619017 |
47126807 |
G |
B15-B19 Viral hepatitis |
0.00045076 |
0.48674 |
0.003692 |
0.01803 |
genotyped |
1.39 |
rs138619017 |
47126807 |
G |
chronic/degenerative neurological problem |
-0.0020969 |
0.12032 |
0.003692 |
0.01803 |
genotyped |
0.708 |
rs138619017 |
47126807 |
G |
type 2 diabetes |
0.00042251 |
0.75864 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
gastro-oesophageal reflux (gord) / gastric reflux |
-0.0027624 |
0.42539 |
0.003692 |
0.01803 |
genotyped |
0.934 |
rs138619017 |
47126807 |
G |
M62 Other disorders of muscle |
0.00034784 |
0.6668 |
0.003692 |
0.01803 |
genotyped |
1.18 |
rs138619017 |
47126807 |
G |
M65 Synovitis and tenosynovitis |
0.0024654 |
0.20241 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
M66 Spontaneous rupture of synovium and tendon |
0.00037174 |
0.54955 |
0.003692 |
0.01803 |
genotyped |
1.34 |
rs138619017 |
47126807 |
G |
M67 Other disorders of synovium and tendon |
0.0006031 |
0.71667 |
0.003692 |
0.01803 |
genotyped |
1.07 |
rs138619017 |
47126807 |
G |
H80-H83 Diseases of inner ear |
-0.0010307 |
0.40062 |
0.003692 |
0.01803 |
genotyped |
0.812 |
rs138619017 |
47126807 |
G |
M50-M54 Other dorsopathies |
-0.0071627 |
0.050565 |
0.003692 |
0.01803 |
genotyped |
0.855 |
rs138619017 |
47126807 |
G |
pneumothorax |
0.00059286 |
0.518 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
neurological injury/trauma |
0.0012438 |
0.3345 |
0.003692 |
0.01803 |
genotyped |
1.25 |
rs138619017 |
47126807 |
G |
C60-C63 Malignant neoplasms of male genital organs |
0.0041703 |
0.36176 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
gout |
-0.00025158 |
0.89973 |
0.003692 |
0.01803 |
genotyped |
0.982 |
rs138619017 |
47126807 |
G |
N70-N77 Inflammatory diseases of female pelvic organs |
0.0032216 |
0.39433 |
0.003692 |
0.01803 |
genotyped |
1.13 |
rs138619017 |
47126807 |
G |
D10-D36 Benign neoplasms |
0.00012941 |
0.8549 |
0.003692 |
0.01803 |
genotyped |
1.08 |
rs138619017 |
47126807 |
G |
testicular problems (not cancer) |
0.001033 |
0.46652 |
0.003692 |
0.01803 |
genotyped |
1.41 |
rs138619017 |
47126807 |
G |
nervous breakdown |
0.00028789 |
0.66699 |
0.003692 |
0.01803 |
genotyped |
1.22 |
rs138619017 |
47126807 |
G |
H43 Disorders of vitreous body |
0.00050377 |
0.61184 |
0.003692 |
0.01803 |
genotyped |
1.17 |
rs138619017 |
47126807 |
G |
H40 Glaucoma |
0.00056792 |
0.74845 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
menorrhagia (unknown cause) |
-0.0016699 |
0.30785 |
0.003692 |
0.01803 |
genotyped |
0.715 |
rs138619017 |
47126807 |
G |
H00-H06 Disorders of eyelid, lacrimal system and orbit |
-0.0024898 |
0.34378 |
0.003692 |
0.01803 |
genotyped |
0.897 |
rs138619017 |
47126807 |
G |
Cheese intake |
-0.0019184 |
0.91106 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Part of a multiple birth |
0.0047769 |
0.063028 |
0.003692 |
0.01803 |
genotyped |
1.24 |
rs138619017 |
47126807 |
G |
Ease of skin tanning |
0.0045839 |
0.74296 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Variation in diet |
-0.0057414 |
0.56143 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Usual walking pace |
-0.012869 |
0.18534 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of vehicles in household |
-0.00095835 |
0.9453 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Skin colour |
0.0043707 |
0.60039 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Pork intake |
0.0017906 |
0.87993 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Salt added to food |
-0.015899 |
0.24695 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Hot drink temperature |
-0.013931 |
0.12896 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Alcohol intake frequency. |
-0.011355 |
0.62795 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Alcohol drinker status |
-0.0046664 |
0.48033 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Processed meat intake |
0.0018572 |
0.91157 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Poultry intake |
-0.016939 |
0.24789 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Beef intake |
-0.005323 |
0.69582 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Lamb/mutton intake |
0.0073764 |
0.52318 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Oily fish intake |
0.0097952 |
0.5099 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Non-oily fish intake |
0.0071229 |
0.58677 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Smoking status |
-0.011909 |
0.26131 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Current tobacco smoking |
-0.01578 |
0.080912 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Comparative body size at age 10 |
-0.0069139 |
0.50136 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Comparative height size at age 10 |
-0.012488 |
0.18372 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Handedness (chirality/laterality) |
0.0048534 |
0.33635 |
0.003692 |
0.01803 |
genotyped |
1.06 |
rs138619017 |
47126807 |
G |
Mean reticulocyte volume |
0.062553 |
0.56244 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Immature reticulocyte fraction |
-0.00023125 |
0.7949 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Reticulocyte percentage |
-0.0014515 |
0.85583 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Reticulocyte count |
4.6764e-05 |
0.89744 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
High light scatter reticulocyte count |
-7.5495e-05 |
0.56704 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Mean sphered cell volume |
0.03134 |
0.65776 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
High light scatter reticulocyte percentage |
-0.0020646 |
0.48396 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Nucleated red blood cell percentage |
-0.0025742 |
0.70842 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Nucleated red blood cell count |
-0.00035755 |
0.51841 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Lymphocyte count |
0.011008 |
0.22681 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Monocyte count |
0.0026999 |
0.24671 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Neutrophill count |
-0.016824 |
0.41721 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Eosinophill count |
0.0030442 |
0.1007 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Basophill count |
0.00048569 |
0.4556 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Lymphocyte percentage |
0.15124 |
0.16113 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Monocyte percentage |
0.030687 |
0.32518 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Neutrophill percentage |
-0.20779 |
0.09874 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Eosinophill percentage |
0.024732 |
0.33683 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Basophill percentage |
0.0088004 |
0.2244 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Mean platelet (thrombocyte) volume |
0.015041 |
0.24512 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Platelet distribution width |
0.0014294 |
0.84009 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Mean corpuscular haemoglobin concentration |
-0.028268 |
0.057051 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Platelet crit |
-0.00084138 |
0.17656 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
White blood cell (leukocyte) count |
0.0003272 |
0.98983 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Mean corpuscular haemoglobin |
-0.018731 |
0.4331 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Platelet count |
-1.3622 |
0.069089 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Mean corpuscular volume |
-0.00078001 |
0.98945 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Red blood cell (erythrocyte) distribution width |
-0.00084509 |
0.95074 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Red blood cell (erythrocyte) count |
0.0052649 |
0.27858 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Haemoglobin concentration |
0.0046472 |
0.74435 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Haematocrit percentage |
0.04968 |
0.23744 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Whole body fat mass |
-0.16526 |
0.20084 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Trunk predicted mass |
-0.035686 |
0.37598 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Trunk fat-free mass |
-0.034692 |
0.40879 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Trunk fat mass |
-0.11218 |
0.11777 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Trunk fat percentage |
-0.20546 |
0.044413 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Body fat percentage |
-0.16462 |
0.063371 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm predicted mass (left) |
-0.0075971 |
0.2037 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm fat-free mass (left) |
-0.0098306 |
0.12096 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm fat mass (left) |
-0.0054937 |
0.57204 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm fat percentage (left) |
-0.11629 |
0.27507 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm predicted mass (right) |
-0.0084412 |
0.13236 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm fat-free mass (right) |
-0.0086436 |
0.14634 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm fat mass (right) |
-0.0040277 |
0.6436 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Arm fat percentage (right) |
-0.10913 |
0.30306 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg predicted mass (left) |
-0.012734 |
0.40784 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg fat-free mass (left) |
-0.014659 |
0.37153 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg fat mass (left) |
-0.024371 |
0.26093 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg fat percentage (left) |
-0.13693 |
0.062629 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Impedance of arm (right) |
0.087572 |
0.86572 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg predicted mass (right) |
-0.0061607 |
0.68733 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg fat-free mass (right) |
-0.0069835 |
0.66879 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Impedance of whole body |
-0.88169 |
0.32907 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Whole body fat-free mass |
-0.069808 |
0.39466 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg fat mass (right) |
-0.02802 |
0.20639 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Impedance of arm (left) |
-0.14541 |
0.78691 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Leg fat percentage (right) |
-0.15675 |
0.042782 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Impedance of leg (left) |
-0.43931 |
0.32111 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Impedance of leg (right) |
-0.49897 |
0.25972 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Basal metabolic rate |
-12.053 |
0.27973 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Body mass index (BMI) |
-0.039022 |
0.55385 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Whole body water mass |
-0.06176 |
0.30687 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Weight |
-0.2446 |
0.2027 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Sitting height |
0.004097 |
0.92923 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Hand grip strength (left) / Hand grip strength (right) |
-0.0031746 |
0.33792 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Body mass index (BMI) |
-0.033748 |
0.61138 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Weight |
-0.24353 |
0.20791 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Standing height |
-0.11016 |
0.10507 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Waist circumference / Hip circumference |
-0.00028395 |
0.77472 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Hip circumference |
-0.11479 |
0.38134 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Waist circumference |
-0.11938 |
0.48766 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Townsend deprivation index at recruitment |
0.017459 |
0.70606 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Dried fruit intake |
0.014253 |
0.55281 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Coffee intake |
-0.068343 |
0.046134 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Water intake |
0.01963 |
0.57463 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Frequency of solarium/sunlamp use |
0.062918 |
0.41765 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Salad / raw vegetable intake |
-0.0079667 |
0.80082 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Time spent watching television (TV) |
-0.0027182 |
0.91398 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of days/week of vigorous physical activity 10+ minutes |
-0.016694 |
0.59916 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of days/week of moderate physical activity 10+ minutes |
1.9183e-06 |
0.99996 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Cereal intake |
0.019419 |
0.6713 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Fresh fruit intake |
-0.0041506 |
0.86327 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Tea intake |
-0.014295 |
0.75826 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Cooked vegetable intake |
-0.012883 |
0.63378 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Bread intake |
-0.043643 |
0.74553 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of days/week walked 10+ minutes |
-0.016258 |
0.60996 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of full brothers |
0.0055326 |
0.77875 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of full sisters |
-0.011097 |
0.55623 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number in household |
0.017475 |
0.31806 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Hand grip strength (left) |
-0.16176 |
0.1618 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Hand grip strength (right) |
-0.13327 |
0.24926 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of self-reported cancers |
-0.0043725 |
0.41109 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of self-reported non-cancer illnesses |
0.010203 |
0.72584 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of operations, self-reported |
-0.0069159 |
0.77916 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Number of treatments/medications taken |
0.044145 |
0.28141 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Sleep duration |
0.04338 |
0.014228 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Mean time to correctly identify matches |
5.0359 |
0.0040006 |
0.003692 |
0.01803 |
genotyped |
- |
rs138619017 |
47126807 |
G |
Pace-maker |
0.00055654 |
0.55862 |
0.003692 |
0.01803 |
genotyped |
1.2 |