TreeWAS – Variant ID: rs7615952

Hospitalization Episode Statistics (HES)

Self-Reported Statistics (SRS)

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Results table

Term	Risk posterior probability	No effect posterior probability	Protective posterior probability
I25.2 Old myocardial infarction	0.000	0.984	0.016
I25.8 Other forms of chronic ischaemic heart disease	0.000	0.986	0.014
I25 Chronic ischaemic heart disease	0.000	0.986	0.014
I25.3 Aneurysm of heart	0.000	0.988	0.011
Z90.5 Acquired absence of kidney	0.000	0.989	0.011
I22.9 Subsequent myocardial infarction of unspecified site	0.000	0.989	0.011
I25.4 Coronary artery aneurysm	0.000	0.990	0.010
I25.6 Silent myocardial ischaemia	0.000	0.990	0.010
I22 Subsequent myocardial infarction	0.000	0.991	0.009
I25.1 Atherosclerotic heart disease	0.000	0.991	0.009
I20-I25 Ischaemic heart diseases	0.000	0.991	0.009
I25.9 Chronic ischaemic heart disease, unspecified	0.000	0.991	0.009
R22.4 Localised swelling, mass and lump, lower limb	0.000	0.991	0.009
I25.5 Ischaemic cardiomyopathy	0.000	0.992	0.008
I21 Acute myocardial infarction	0.000	0.992	0.008
I22.0 Subsequent myocardial infarction of anterior wall	0.000	0.992	0.008
I21.0 Acute transmural myocardial infarction of anterior wall	0.000	0.992	0.008
I21.9 Acute myocardial infarction, unspecified	0.000	0.992	0.008
M23.25 Derangement of meniscus due to old tear or injury (Posterior horn of lateral meniscus)	0.000	0.993	0.007
I21.3 Acute transmural myocardial infarction of unspecified site	0.000	0.993	0.007
N94.6 Dysmenorrhoea, unspecified	0.000	0.993	0.007
F31.0 Bipolar affective disorder, current episode hypomanic	0.000	0.993	0.006
F31 Bipolar affective disorder	0.000	0.994	0.006
I23 Certain current complications following acute myocardial infarction	0.000	0.994	0.006
I21.2 Acute transmural myocardial infarction of other sites	0.000	0.994	0.006
K27.9 Unspecified as acute or chronic, without haemorrhage or perforation	0.000	0.994	0.006
F31.1 Bipolar affective disorder, current episode manic without psychotic symptoms	0.000	0.994	0.006
I25.0 Atherosclerotic cardiovascular disease, so described	0.000	0.994	0.006
F31.3 Bipolar affective disorder, current episode mild or moderate depression	0.000	0.994	0.006
I21.X Presumed acute myicardial infaction (unconfirmed)	0.000	0.994	0.006
F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms	0.000	0.994	0.006
F31.6 Bipolar affective disorder, current episode mixed	0.000	0.994	0.006
I22.8 Subsequent myocardial infarction of other sites	0.000	0.994	0.005
F31.4 Bipolar affective disorder, current episode severe depression without psychotic symptoms	0.000	0.994	0.006
S62.30 Fracture of other metacarpal bone (closed)	0.005	0.995	0.000
F31.7 Bipolar affective disorder, currently in remission	0.000	0.995	0.005
Q61.2 Polycystic kidney, adult type	0.005	0.995	0.000
F31.8 Other bipolar affective disorders	0.000	0.995	0.005
I23.6 Thrombosis of atrium, auricular appendage and ventricle as current complications following acute myocardial infarction	0.000	0.995	0.005
I23.5 Rupture of papillary muscle as current complication following acute myocardial infarction	0.000	0.995	0.005
I23.4 Rupture of chordae tendineae as current complication following acute myocardial infarction	0.000	0.995	0.005
I23.3 Rupture of cardiac wall without haemopericardium as current complication following acute myocardial infarction	0.000	0.995	0.005
I23.2 Ventricular septal defect as current complication following acute myocardial infarction	0.000	0.995	0.005
I23.1 Atrial septal defect as current complication following acute myocardial infarction	0.000	0.995	0.005
I23.0 Haemopericardium as current complication following acute myocardial infarction	0.000	0.995	0.005
I24 Other acute ischaemic heart diseases	0.000	0.995	0.005
Q61.3 Polycystic kidney, unspecified	0.005	0.995	0.000
I23.8 Other current complications following acute myocardial infarction	0.000	0.995	0.005
F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms	0.000	0.995	0.004
Q61 Cystic kidney disease	0.004	0.995	0.000
I22.1 Subsequent myocardial infarction of inferior wall	0.000	0.995	0.004
M65.34 Trigger finger-Hand	0.004	0.996	0.000
H60.9 Otitis externa, unspecified	0.000	0.996	0.004
I24.0 Coronary thrombosis not resulting in myocardial infarction	0.000	0.996	0.004
Q23.1 Congenital insufficiency of aortic valve	0.004	0.996	0.000
H02.0 Entropion and trichiasis of eyelid	0.000	0.996	0.004
I24.1 Dressler's syndrome	0.000	0.996	0.004
Q23 Congenital malformations of aortic and mitral valves	0.004	0.996	0.000
N48.1 Balanoposthitis	0.000	0.996	0.004
Q28.2 Arteriovenous malformation of cerebral vessels	0.004	0.996	0.000
N48.0 Leukoplakia of penis	0.000	0.996	0.004
Q61.5 Medullary cystic kidney	0.003	0.996	0.000
C53.9 Cervix uteri, unspecified	0.004	0.996	0.000
Q61.9 Cystic kidney disease, unspecified	0.003	0.996	0.000
F31.9 Bipolar affective disorder, unspecified	0.000	0.996	0.004
Q61.8 Other cystic kidney diseases	0.003	0.996	0.000
Q61.4 Renal dysplasia	0.003	0.996	0.000
Q61.1 Polycystic kidney, infantile type	0.003	0.996	0.000
R49.0 Dysphonia	0.000	0.997	0.003
Q28 Other congenital malformations of circulatory system	0.003	0.997	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
I21.1 Acute transmural myocardial infarction of inferior wall	0.000	0.997	0.003
M65.3 Trigger finger	0.003	0.997	0.000
N48 Other disorders of penis	0.000	0.997	0.003
Z35.2 Supervision of pregnancy with other poor reproductive or obstetric history	0.003	0.997	0.000
N73.9 Female pelvic inflammatory disease, unspecified	0.003	0.997	0.000
I20 Angina pectoris	0.000	0.997	0.003
R93.4 Abnormal findings on diagnostic imaging of urinary organs	0.000	0.997	0.003
M65.90 Synovitis and tenosynovitis, unspecified (Multiple sites)	0.003	0.997	0.000
M65.96 Synovitis and tenosynovitis, unspecified (Lower leg)	0.000	0.997	0.003
Q61.0 Congenital single renal cyst	0.003	0.997	0.000
N48.9 Disorder of penis, unspecified	0.000	0.997	0.003
I20.1 Angina pectoris with documented spasm	0.000	0.997	0.003
N48.6 Balanitis xerotica obliterans	0.000	0.997	0.003
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.003	0.997	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.003	0.997	0.000
Q23.4 Hypoplastic left heart syndrome	0.003	0.997	0.000
Q23.3 Congenital mitral insufficiency	0.003	0.997	0.000
Q23.2 Congenital mitral stenosis	0.003	0.997	0.000
Q23.0 Congenital stenosis of aortic valve	0.003	0.997	0.000
Q60-Q64 Congenital malformations of the urinary system	0.003	0.997	0.000
M46.96 Inflammatory spondylopathy, unspecified (Lumbar region)	0.003	0.997	0.000
C53 Malignant neoplasm of cervix uteri	0.003	0.997	0.000
M65.91 Synovitis and tenosynovitis, unspecified (Shoulder region)	0.003	0.997	0.000
M77.47 Metatarsalgia-Ankle/Foot	0.000	0.997	0.003
G37.9 Demyelinating disease of central nervous system, unspecified	0.000	0.997	0.003
S62.3 Fracture of other metacarpal bone	0.003	0.997	0.000
N90.4 Leukoplakia of vulva	0.003	0.997	0.000
Q25 Congenital malformations of great arteries	0.003	0.997	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.003	0.997	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.003	0.997	0.000
Q28.3 Other malformations of cerebral vessels	0.003	0.997	0.000
Q28.1 Other malformations of precerebral vessels	0.003	0.997	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.003	0.997	0.000
M21.16 Varus deformity, not elsewhere classified (Lower leg)	0.003	0.997	0.000
M65.9 Synovitis and tenosynovitis, unspecified	0.003	0.997	0.000
I24.9 Acute ischaemic heart disease, unspecified	0.000	0.997	0.003
N48.2 Other inflammatory disorders of penis	0.000	0.997	0.003
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.003	0.997	0.000
Q26 Congenital malformations of great veins	0.003	0.997	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.003	0.997	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.003	0.997	0.000
I21.4 Acute subendocardial myocardial infarction	0.000	0.997	0.003
M65.93 Synovitis and tenosynovitis, unspecified (Forearm)	0.003	0.997	0.000
N48.5 Ulcer of penis	0.000	0.997	0.003
M65.39 Trigger finger-Site unspec	0.002	0.997	0.000
M65.38 Trigger finger-Other	0.002	0.997	0.000
M65.37 Trigger finger-Ankle/foot	0.002	0.997	0.000
M65.36 Trigger finger-Lower leg	0.002	0.997	0.000
M65.35 Trigger finger-Pelvic/thigh	0.002	0.997	0.000
M65.33 Trigger finger-Forearm	0.002	0.997	0.000
M65.32 Trigger finger-Upper arm	0.002	0.997	0.000
M65.31 Trigger finger-Shldr region	0.002	0.997	0.000
M65.30 Trigger finger-Mult sites	0.002	0.997	0.000
H26.4 After-cataract	0.000	0.997	0.003
M46.9 Inflammatory spondylopathy, unspecified	0.003	0.997	0.000
M46.90 Inflammatory spondylopathy, unspecified (Multiple sites in spine)	0.003	0.997	0.000
S52.60 Fracture of lower end of both ulna and radius (closed)	0.000	0.997	0.003
N48.3 Priapism	0.000	0.997	0.002
Q27 Other congenital malformations of peripheral vascular system	0.002	0.997	0.000
T85.8 Other complications of internal prosthetic devices, implants and grafts, not elsewhere classified	0.000	0.997	0.003
C53.0 Endocervix	0.002	0.997	0.000
F40.2 Specific (isolated) phobias	0.003	0.997	0.000
H80.9 Otosclerosis, unspecified	0.000	0.997	0.002
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.997	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
K27 Peptic ulcer, site unspecified	0.000	0.998	0.002
K14.9 Disease of tongue, unspecified	0.002	0.998	0.000
Y86 Sequelae of other accidents	0.000	0.998	0.002
M41.96 Scoliosis, unspecified (Lumbar region)	0.000	0.998	0.002
M65.99 Synovitis and tenosynovitis, unspecified (Site unspecified)	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
M65.94 Synovitis and tenosynovitis, unspecified (Hand)	0.002	0.998	0.000
Q50.4 Embryonic cyst of Fallopian tube	0.002	0.998	0.000
W21.9 Unspecified place	0.002	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.002	0.998	0.000
M65.92 Synovitis and tenosynovitis, unspecified (Upper arm)	0.002	0.998	0.000
C53.8 Overlapping lesion of cervix uteri	0.002	0.998	0.000
C53.1 Exocervix	0.002	0.998	0.000
Q21.0 Ventricular septal defect	0.002	0.998	0.000
Q25.4 Other congenital malformations of aorta	0.002	0.998	0.000
G37 Other demyelinating diseases of central nervous system	0.000	0.998	0.002
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
G37.3 Acute transverse myelitis in demyelinating disease of central nervous system	0.000	0.998	0.002
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.002	0.998	0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.002	0.998	0.000
Q25.8 Other congenital malformations of great arteries	0.002	0.998	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.998	0.000
Q25.6 Stenosis of pulmonary artery	0.002	0.998	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.998	0.000
Q25.3 Stenosis of aorta	0.002	0.998	0.000
Q25.2 Atresia of aorta	0.002	0.998	0.000
Q25.1 Coarctation of aorta	0.002	0.998	0.000
Q25.0 Patent ductus arteriosus	0.002	0.998	0.000
M65 Synovitis and tenosynovitis	0.002	0.998	0.000
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
M65.98 Synovitis and tenosynovitis, unspecified (Other)	0.002	0.998	0.000
M94.26 Chondromalacia (Lower leg)	0.002	0.998	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
S62.31 Fracture of other metacarpal bone (open)	0.002	0.998	0.000
I20.0 Unstable angina	0.000	0.998	0.002
Q64 Other congenital malformations of urinary system	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
M46.99 Inflammatory spondylopathy, unspecified (Site unspecified)	0.002	0.998	0.000
M46.97 Inflammatory spondylopathy, unspecified (Lumbosacral region)	0.002	0.998	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.002	0.998	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
Q20.6 Isomerism of atrial appendages	0.002	0.998	0.000
Q20.5 Discordant atrioventricular connexion	0.002	0.998	0.000
Q20.4 Double inlet ventricle	0.002	0.998	0.000
Q20.3 Discordant ventriculoarterial connexion	0.002	0.998	0.000
Q20.2 Double outlet left ventricle	0.002	0.998	0.000
Q20.1 Double outlet right ventricle	0.002	0.998	0.000
Q20.0 Common arterial trunk	0.002	0.998	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.002	0.998	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.002	0.998	0.000
Q22.6 Hypoplastic right heart syndrome	0.002	0.998	0.000
Q22.5 Ebstein's anomaly	0.002	0.998	0.000
Q22.4 Congenital tricuspid stenosis	0.002	0.998	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.002	0.998	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.002	0.998	0.000
Q22.1 Congenital pulmonary valve stenosis	0.002	0.998	0.000
Q22.0 Pulmonary valve atresia	0.002	0.998	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.002	0.998	0.000
Q26.8 Other congenital malformations of great veins	0.002	0.998	0.000
Q26.6 Portal vein-hepatic artery fistula	0.002	0.998	0.000
Q26.5 Anomalous portal venous connexion	0.002	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.002	0.998	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.002	0.998	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.002	0.998	0.000
Q26.1 Persistent left superior vena cava	0.002	0.998	0.000
Q26.0 Congenital stenosis of vena cava	0.002	0.998	0.000
Q24 Other congenital malformations of heart	0.002	0.998	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
Q90 Down's syndrome	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
M46.98 Inflammatory spondylopathy, unspecified (Sacral and sacrococcygeal region)	0.002	0.998	0.000
M46.95 Inflammatory spondylopathy, unspecified (Thoracolumbar region)	0.002	0.998	0.000
M46.94 Inflammatory spondylopathy, unspecified (Thoracic region)	0.002	0.998	0.000
M46.93 Inflammatory spondylopathy, unspecified (Cervicothoracic region)	0.002	0.998	0.000
M46.91 Inflammatory spondylopathy, unspecified (Occipito-atlanto-axial region)	0.002	0.998	0.000
M65.95 Synovitis and tenosynovitis, unspecified (Pelvic region and thigh)	0.002	0.998	0.000
Q27.4 Congenital phlebectasia	0.002	0.998	0.000
Q27.2 Other congenital malformations of renal artery	0.002	0.998	0.000
Q27.1 Congenital renal artery stenosis	0.002	0.998	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.002	0.998	0.000
I98.2 Oesophageal varices in diseases classified elsewhere	0.000	0.998	0.002
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q52 Other congenital malformations of female genitalia	0.002	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.998	0.001
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
M80.98 Unspecified osteoporosis with pathological fracture (Other)	0.002	0.998	0.000
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
M94.2 Chondromalacia	0.002	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.002	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.002	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.002	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.002	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.002	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
Q21.8 Other congenital malformations of cardiac septa	0.002	0.998	0.000
Q21.4 Aortopulmonary septal defect	0.002	0.998	0.000
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
Q21.2 Atrioventricular septal defect	0.002	0.998	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
I24.8 Other forms of acute ischaemic heart disease	0.000	0.998	0.002
K27.7 Chronic without haemorrhage or perforation	0.000	0.998	0.002
K27.6 Chronic or unspecified with both haemorrhage and perforation	0.000	0.998	0.002
K27.5 Chronic or unspecified with perforation	0.000	0.998	0.002
K27.4 Chronic or unspecified with haemorrhage	0.000	0.998	0.002
K27.2 Acute with both haemorrhage and perforation	0.000	0.998	0.002
K27.1 Acute with perforation	0.000	0.998	0.002
K27.0 Acute with haemorrhage	0.000	0.998	0.002
Q96 Turner's syndrome	0.002	0.998	0.000
Q52.4 Other congenital malformations of vagina	0.002	0.998	0.000
C51-C58 Malignant neoplasms of female genital organs	0.002	0.998	0.000
M94.8 Other specified disorders of cartilage	0.002	0.998	0.000
N41.9 Inflammatory disease of prostate, unspecified	0.000	0.998	0.002
G35 Multiple sclerosis	0.000	0.998	0.002
M46 Other inflammatory spondylopathies	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
M94.86 Other specified disorders of cartilage (Lower leg)	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
C79.2 Secondary malignant neoplasm of skin	0.002	0.998	0.000
Q37 Cleft palate with cleft lip	0.002	0.998	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.002	0.998	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.002	0.998	0.000
G37.5 Concentric sclerosis [Balo]	0.000	0.998	0.002
G37.4 Subacute necrotising myelitis	0.000	0.998	0.002
G37.2 Central pontine myelinolysis	0.000	0.998	0.002
G37.1 Central demyelination of corpus callosum	0.000	0.998	0.002
G37.0 Diffuse sclerosis	0.000	0.998	0.002
M46.1 Sacro-iliitis, not elsewhere classified	0.002	0.998	0.000
Q62.8 Other congenital malformations of ureter	0.002	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.002	0.998	0.000
Q62.6 Malposition of ureter	0.002	0.998	0.000
Q62.4 Agenesis of ureter	0.002	0.998	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.002	0.998	0.000
Q62.2 Congenital megaloureter	0.002	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.002	0.998	0.000
Q62.0 Congenital hydronephrosis	0.002	0.998	0.000
Q90.9 Down's syndrome, unspecified	0.002	0.998	0.000
C55 Malignant neoplasm of uterus, part unspecified	0.002	0.998	0.000
Q66 Congenital deformities of feet	0.002	0.998	0.000
M65.1 Other infective (teno)synovitis	0.002	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.002	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.002	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.002	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.002	0.998	0.000
Q98.5 Karyotype 47,XYY	0.002	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.002	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.002	0.998	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.002	0.998	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.002	0.998	0.000
M46.3 Infection of intervertebral disk (pyogenic)	0.002	0.998	0.000
Q62.5 Duplication of ureter	0.002	0.998	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.002	0.998	0.000
M94 Other disorders of cartilage	0.002	0.998	0.000
Q12 Congenital lens malformations	0.002	0.998	0.000
Q89 Other congenital malformations, not elsewhere classified	0.002	0.998	0.000
M46.44 Discitis, unspecified (Thoracic region)	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.002	0.998	0.000
Q50.6 Other congenital malformatons of Fallopian tube and broad ligament	0.002	0.998	0.000
Q50.3 Other congenital malformations of ovary	0.002	0.998	0.000
Q50.2 Congenital torsion of ovary	0.002	0.998	0.000
Q50.1 Developmental ovarian cyst	0.002	0.998	0.000
Q50.0 Congenital absence of ovary	0.002	0.998	0.000
F40 Phobic anxiety disorders	0.002	0.998	0.000
Q55 Other congenital malformations of male genital organs	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
M41.95 Scoliosis, unspecified (Thoracolumbar region)	0.000	0.998	0.002
M46.19 Sacroiliitis, not elsewhere classified-Site unspe	0.002	0.998	0.000
M46.36 Infection of intervertebral disc (pyogenic) (Lumbar region)	0.002	0.998	0.000
K27.3 Acute without haemorrhage or perforation	0.000	0.998	0.002
M41.9 Scoliosis, unspecified	0.000	0.998	0.002
M65.2 Calcific tendinitis	0.002	0.998	0.000
M65.0 Abscess of tendon sheath	0.002	0.998	0.000
Q27.3 Peripheral arteriovenous malformation	0.002	0.998	0.000
Q50.5 Embryonic cyst of broad ligament	0.002	0.998	0.000
Q36 Cleft lip	0.002	0.998	0.000
Q35 Cleft palate	0.002	0.998	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.002	0.998	0.000
F40.9 Phobic anxiety disorder, unspecified	0.002	0.998	0.000
M46.4 Discitis, unspecified	0.002	0.998	0.000
Q67.6 Pectus excavatum	0.002	0.998	0.000
Q89.3 Situs inversus	0.002	0.998	0.000
N48.4 Impotence of organic origin	0.000	0.998	0.002
Q12.0 Congenital cataract	0.002	0.998	0.000
Q24.6 Congenital heart block	0.002	0.998	0.000
Q24.4 Congenital subaortic stenosis	0.002	0.998	0.000
Q24.3 Pulmonary infundibular stenosis	0.002	0.998	0.000
Q24.2 Cor triatriatum	0.002	0.998	0.000
Q24.1 Levocardia	0.002	0.998	0.000
Q24.0 Dextrocardia	0.002	0.998	0.000
Q38.8 Other congenital malformations of pharynx	0.002	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.998	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.002	0.998	0.000
Q38.3 Other congenital malformations of tongue	0.002	0.998	0.000
Q38.2 Macroglossia	0.002	0.998	0.000
Q38.1 Ankyloglossia	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.001	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.001	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.001	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.001	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.001	0.998	0.000
Q64.4 Malformation of urachus	0.001	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.001	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.001	0.998	0.000
Q64.0 Epispadias	0.001	0.998	0.000
Q66.8 Other congenital deformities of feet	0.002	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.002	0.998	0.000
Q33 Congenital malformations of lung	0.002	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.002	0.998	0.000
Q31 Congenital malformations of larynx	0.002	0.998	0.000
Q30 Congenital malformations of nose	0.002	0.998	0.000
Q83 Congenital malformations of breast	0.002	0.998	0.000
M94.9 Disorder of cartilage, unspecified	0.002	0.998	0.000
Q90.2 Trisomy 21, translocation	0.002	0.998	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.002	0.998	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.002	0.998	0.000
Q84 Other congenital malformations of integument	0.002	0.998	0.000
Q81 Epidermolysis bullosa	0.002	0.998	0.000
Q80 Congenital ichthyosis	0.002	0.998	0.000
H60 Otitis externa	0.000	0.998	0.002
C54.9 Corpus uteri, unspecified	0.002	0.998	0.000
G37.8 Other specified demyelinating diseases of central nervous system	0.000	0.998	0.002
M94.0 Chondrocostal junction syndrome [Tietze]	0.002	0.998	0.000
N48.8 Other specified disorders of penis	0.000	0.998	0.002
M41.99 Scoliosis, unspecified (Site unspecified)	0.000	0.998	0.002
M94.88 Other specified disorders of cartilage (Other)	0.002	0.998	0.000
M94.96 Disorder of cartilage, unspecified (Lower leg)	0.002	0.998	0.000
G12.2 Motor neuron disease	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.002	0.998	0.000
Q45.8 Other specified congenital malformations of digestive system	0.002	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.002	0.998	0.000
Q45.1 Annular pancreas	0.002	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.002	0.998	0.000
Q52.9 Congenital malformation of female genitalia, unspecified	0.002	0.998	0.000
Q52.8 Other specified congenital malformations of female genitalia	0.002	0.998	0.000
Q52.7 Other congenital malformations of vulva	0.002	0.998	0.000
Q52.6 Congenital malformation of clitoris	0.002	0.998	0.000
Q52.5 Fusion of labia	0.002	0.998	0.000
Q52.3 Imperforate hymen	0.002	0.998	0.000
Q52.2 Congenital rectovaginal fistula	0.002	0.998	0.000
Q52.1 Doubling of vagina	0.002	0.998	0.000
Q52.0 Congenital absence of vagina	0.002	0.998	0.000
Q60.6 Potter's syndrome	0.001	0.998	0.001
Q60.5 Renal hypoplasia, unspecified	0.001	0.998	0.001
Q60.4 Renal hypoplasia, bilateral	0.001	0.998	0.001
Q60.3 Renal hypoplasia, unilateral	0.001	0.998	0.001
Q60.1 Renal agenesis, bilateral	0.001	0.998	0.001
Q15 Other congenital malformations of eye	0.002	0.998	0.000
Q60.2 Renal agenesis, unspecified	0.001	0.998	0.000
Z49.0 Preparatory care for dialysis	0.000	0.998	0.002
C52 Malignant neoplasm of vagina	0.002	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.002	0.998	0.000
Q04 Other congenital malformations of brain	0.002	0.998	0.000
Q03 Congenital hydrocephalus	0.002	0.998	0.000
Q01 Encephalocele	0.002	0.998	0.000
Q00 Anencephaly and similar malformations	0.002	0.998	0.000
Q02 Microcephaly	0.002	0.998	0.000
M41.94 Scoliosis, unspecified (Thoracic region)	0.000	0.998	0.002
M46.18 Sacroiliitis, not elsewhere classified-Sacral/sacrococ	0.002	0.998	0.000
M94.29 Chondromalacia (Site unspecified)	0.002	0.998	0.000
M94.28 Chondromalacia (Other)	0.002	0.998	0.000
M94.27 Chondromalacia (Ankle and foot)	0.002	0.998	0.000
M94.25 Chondromalacia (Pelvic region and thigh)	0.002	0.998	0.000
M94.24 Chondromalacia (Hand)	0.002	0.998	0.000
M94.23 Chondromalacia (Forearm)	0.002	0.998	0.000
M94.22 Chondromalacia (Upper arm)	0.002	0.998	0.000
M94.21 Chondromalacia (Shoulder region)	0.002	0.998	0.000
M94.20 Chondromalacia (Multiple sites)	0.002	0.998	0.000
Q37.9 Unspecified cleft palate with unilateral cleft lip	0.002	0.998	0.000
Q39.4 Oesophageal web	0.002	0.998	0.000
Q91.7 Patau's syndrome, unspecified	0.001	0.998	0.000
Q91.6 Trisomy 13, translocation	0.001	0.998	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.001	0.998	0.000
Q91.3 Edwards' syndrome, unspecified	0.001	0.998	0.000
Q91.2 Trisomy 18, translocation	0.001	0.998	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.001	0.998	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.001	0.998	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.001	0.998	0.000
Q92.7 Triploidy and polyploidy	0.001	0.998	0.000
Q92.6 Extra marker chromosomes	0.001	0.998	0.000
Q92.5 Duplications with other complex rearrangements	0.001	0.998	0.000
Q92.4 Duplications seen only at prometaphase	0.001	0.998	0.000
Q92.3 Minor partial trisomy	0.001	0.998	0.000
Q92.2 Major partial trisomy	0.001	0.998	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.001	0.998	0.000
Q93.9 Deletion from autosomes, unspecified	0.001	0.998	0.000
Q93.8 Other deletions from the autosomes	0.001	0.998	0.000
Q93.7 Deletions with other complex rearrangements	0.001	0.998	0.000
Q93.6 Deletions seen only at prometaphase	0.001	0.998	0.000
Q93.5 Other deletions of part of a chromosome	0.001	0.998	0.000
Q93.4 Deletion of short arm of chromosome 5	0.001	0.998	0.000
Q93.3 Deletion of short arm of chromosome 4	0.001	0.998	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.001	0.998	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.001	0.998	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.001	0.998	0.000
Q95.8 Other balanced rearrangements and structural markers	0.001	0.998	0.000
Q95.5 Individuals with autosomal fragile site	0.001	0.998	0.000
Q95.4 Individuals with marker heterochromatin	0.001	0.998	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.001	0.998	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.001	0.998	0.000
Q95.1 Chromosome inversion in normal individual	0.001	0.998	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.001	0.998	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.001	0.998	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.001	0.998	0.000
Q97.3 Female with 46,XY karyotype	0.001	0.998	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.001	0.998	0.000
Q97.1 Female with more than three X chromosomes	0.001	0.998	0.000
Q97.0 Karyotype 47,XXX	0.001	0.998	0.000
Q99.9 Chromosomal abnormality, unspecified	0.001	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.001	0.998	0.000
Q99.2 Fragile X chromosome	0.001	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.001	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.001	0.998	0.000
C51 Malignant neoplasm of vulva	0.002	0.998	0.000
C56 Malignant neoplasm of ovary	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
Q14 Congenital malformations of posterior segment of eye	0.002	0.998	0.000
Q13 Congenital malformations of anterior segment of eye	0.002	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
Q53 Undescended testicle	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.001	0.998	0.001
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.002	0.998	0.000
Q73 Reduction defects of unspecified limb	0.002	0.998	0.000
Q72 Reduction defects of lower limb	0.002	0.998	0.000
Q71 Reduction defects of upper limb	0.002	0.998	0.000
Q70 Syndactyly	0.002	0.998	0.000
Q69 Polydactyly	0.002	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
F40.8 Other phobic anxiety disorders	0.002	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.001	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.001	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.001	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.001	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.001	0.998	0.000
Q96.0 Karyotype 45,X	0.001	0.998	0.000
D24 Benign neoplasm of breast	0.000	0.998	0.002
M94.09 Chondrocostal junction syndrome [Tietze]-Site unspec	0.002	0.998	0.000
M94.89 Other specified disorders of cartilage (Site unspecified)	0.002	0.998	0.000
Q66.7 Pes cavus	0.002	0.998	0.000
Z04.8 Examination and observation for other specified reasons	0.000	0.998	0.002
C57 Malignant neoplasm of other and unspecified female genital organs	0.002	0.998	0.000
C58 Malignant neoplasm of placenta	0.002	0.998	0.000
Q05 Spina bifida	0.002	0.998	0.000
W21 Striking against or struck by sports equipment	0.002	0.998	0.000
M65.14 Other infective (teno)synovitis (Hand)	0.002	0.998	0.000

This table lists the top 500 terms ordered by p(effect).

The full results table can be downloaded from this page.

The TreeWAS Database is the result of research conducted at the Oxford Big Data Institute at the University of Oxford.

This research has been conducted using the UK Biobank Resource (application number 10625). This work uses data provided by patients and collected by the NHS as part of their care and support.

This research has been conducted with the support of the Wellcome Trust (100956/Z/13/Z and 090532/Z/09/Z and 100308/Z/12/Z), the Danish National Research Foundation, Takeda, the Medical Research Council (MC_UU_12010/3), the Oak Foundation (OCAY-15-520), the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC), the Wellcome Trust/Royal Society (204290/Z/16/Z) and the Li Ka Shing Foundation.

Variant-specific associations