TreeWAS – Variant ID: rs2318131

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
D86.0 Sarcoidosis of lung	0.028	0.972	0.000
D86 Sarcoidosis	0.026	0.974	0.000
D80-D89 Certain disorders involving the immune mechanism	0.025	0.975	0.000
D80 Immunodeficiency with predominantly antibody defects	0.025	0.975	0.000
D84 Other immunodeficiencies	0.023	0.977	0.000
D86.3 Sarcoidosis of skin	0.021	0.979	0.000
D80.1 Nonfamilial hypogammaglobulinaemia	0.021	0.979	0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.021	0.979	0.000
D12.3 Transverse colon	0.000	0.979	0.021
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.020	0.979	0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.020	0.979	0.000
D84.9 Immunodeficiency, unspecified	0.020	0.980	0.000
D83 Common variable immunodeficiency	0.020	0.980	0.000
D86.8 Sarcoidosis of other and combined sites	0.020	0.980	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.020	0.980	0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.019	0.981	0.000
D84.1 Defects in the complement system	0.019	0.981	0.000
D86.1 Sarcoidosis of lymph nodes	0.018	0.982	0.000
G45.4 Transient global amnesia	0.018	0.982	0.000
D84.8 Other specified immunodeficiencies	0.018	0.982	0.000
D81 Combined immunodeficiencies	0.018	0.982	0.000
D80.8 Other immunodeficiencies with predominantly antibody defects	0.018	0.982	0.000
D80.7 Transient hypogammaglobulinaemia of infancy	0.018	0.982	0.000
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.018	0.982	0.000
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.018	0.982	0.000
D80.0 Hereditary hypogammaglobulinaemia	0.018	0.982	0.000
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.017	0.983	0.000
D83.9 Common variable immunodeficiency, unspecified	0.017	0.983	0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.017	0.983	0.000
D82 Immunodeficiency associated with other major defects	0.016	0.983	0.000
D86.9 Sarcoidosis, unspecified	0.016	0.984	0.000
D83.8 Other common variable immunodeficiencies	0.014	0.985	0.000
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells	0.014	0.985	0.000
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders	0.014	0.985	0.000
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function	0.014	0.985	0.000
H81.1 Benign paroxysmal vertigo	0.014	0.986	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.014	0.986	0.000
D81.9 Combined immunodeficiency, unspecified	0.013	0.987	0.000
D81.8 Other combined immunodeficiencies	0.013	0.987	0.000
D81.7 Major histocompatibility complex class II deficiency	0.013	0.987	0.000
D81.6 Major histocompatibility complex class I deficiency	0.013	0.987	0.000
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.013	0.987	0.000
D81.4 Nezelof's syndrome	0.013	0.987	0.000
D81.3 Adenosine deaminase [ADA] deficiency	0.013	0.987	0.000
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.013	0.987	0.000
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.013	0.987	0.000
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.013	0.987	0.000
D89.1 Cryoglobulinaemia	0.012	0.988	0.000
D89.3 Immune reconstitution syndrome	0.012	0.988	0.000
D82.9 Immunodeficiency associated with major defect, unspecified	0.012	0.988	0.000
D82.8 Immunodeficiency associated with other specified major defects	0.012	0.988	0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.012	0.988	0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.012	0.988	0.000
D82.2 Immunodeficiency with short-limbed stature	0.012	0.988	0.000
D82.0 Wiskott-Aldrich syndrome	0.012	0.988	0.000
D89.0 Polyclonal hypergammaglobulinaemia	0.011	0.988	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.011	0.989	0.000
D82.1 Di George's syndrome	0.010	0.989	0.000
D35.1 Parathyroid gland	0.010	0.990	0.000
H81 Disorders of vestibular function	0.009	0.991	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.008	0.991	0.000
R25.3 Fasciculation	0.000	0.992	0.008
D35.0 Adrenal gland	0.008	0.992	0.000
D35 Benign neoplasm of other and unspecified endocrine glands	0.008	0.992	0.000
H81.3 Other peripheral vertigo	0.008	0.992	0.000
H81.9 Disorder of vestibular function, unspecified	0.008	0.992	0.000
H81.2 Vestibular neuronitis	0.007	0.993	0.000
N86 Erosion and ectropion of cervix uteri	0.000	0.993	0.007
H81.8 Other disorders of vestibular function	0.007	0.993	0.000
H81.4 Vertigo of central origin	0.007	0.993	0.000
D35.2 Pituitary gland	0.007	0.993	0.000
N18.2 Chronic kidney disease, stage 2	0.006	0.994	0.000
I60.9 Subarachnoid haemorrhage, unspecified	0.000	0.994	0.006
R25.8 Other and unspecified abnormal involuntary movements	0.000	0.994	0.006
O20.9 Haemorrhage in early pregnancy, unspecified	0.006	0.994	0.000
N18.3 Chronic kidney disease, stage 3	0.006	0.994	0.000
D35.9 Endocrine gland, unspecified	0.006	0.994	0.000
D35.8 Pluriglandular involvement	0.006	0.994	0.000
D35.7 Other specified endocrine glands	0.006	0.994	0.000
D35.6 Aortic body and other paraganglia	0.006	0.994	0.000
D35.5 Carotid body	0.006	0.994	0.000
D35.4 Pineal gland	0.006	0.994	0.000
D35.3 Craniopharyngeal duct	0.006	0.994	0.000
Q21.1 Atrial septal defect	0.000	0.994	0.006
R25 Abnormal involuntary movements	0.000	0.994	0.006
N18 Chronic renal failure	0.006	0.994	0.000
N18.4 Chronic kidney disease, stage 4	0.005	0.995	0.000
Q21 Congenital malformations of cardiac septa	0.000	0.995	0.005
N18.5 Chronic kidney disease, stage 5	0.005	0.995	0.000
I60.2 Subarachnoid haemorrhage from anterior communicating artery	0.000	0.995	0.005
N03.9 Unspecified	0.005	0.995	0.000
D76.3 Other histiocytosis syndromes	0.000	0.995	0.005
S12.20 Fracture of other specified cervical vertebra (closed)	0.000	0.995	0.005
N18.1 Chronic kidney disease, stage 1	0.005	0.995	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.000	0.995	0.004
Q21.3 Tetralogy of Fallot	0.000	0.995	0.004
Q27 Other congenital malformations of peripheral vascular system	0.000	0.996	0.004
G82.2 Paraplegia, unspecified	0.000	0.996	0.004
R25.0 Abnormal head movements	0.000	0.996	0.004
I60 Subarachnoid haemorrhage	0.000	0.996	0.004
Q27.3 Peripheral arteriovenous malformation	0.000	0.996	0.004
S42.40 Fracture of lower end of humerus (closed)	0.000	0.996	0.004
H16.9 Keratitis, unspecified	0.004	0.996	0.000
N18.9 Chronic renal failure, unspecified	0.004	0.996	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.000	0.996	0.004
Q21.8 Other congenital malformations of cardiac septa	0.000	0.996	0.004
Q21.4 Aortopulmonary septal defect	0.000	0.996	0.004
Q21.2 Atrioventricular septal defect	0.000	0.996	0.004
Q21.0 Ventricular septal defect	0.000	0.996	0.004
H53.0 Amblyopia ex anopsia	0.004	0.996	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.000	0.996	0.004
I60.3 Subarachnoid haemorrhage from posterior communicating artery	0.000	0.996	0.004
R25.1 Tremor, unspecified	0.000	0.996	0.004
Q24 Other congenital malformations of heart	0.000	0.996	0.004
Z87.5 Personal history of complications of pregnancy, childbirth and the puerperium	0.004	0.996	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.000	0.996	0.004
E10.9 Without complications	0.000	0.996	0.004
Q24.5 Malformation of coronary vessels	0.000	0.996	0.004
M54.64 Pain in thoracic spine (Thoracic region)	0.000	0.996	0.004
I60.8 Other subarachnoid haemorrhage	0.000	0.996	0.004
M22.8 Other disorders of patella	0.004	0.996	0.000
R25.2 Cramp and spasm	0.000	0.996	0.004
G82.5 Tetraplegia, unspecified	0.000	0.996	0.004
Q24.9 Congenital malformation of the heart, unspecified	0.000	0.996	0.004
Q27.4 Congenital phlebectasia	0.000	0.997	0.003
Q27.2 Other congenital malformations of renal artery	0.000	0.997	0.003
Q27.1 Congenital renal artery stenosis	0.000	0.997	0.003
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.000	0.997	0.003
N03 Chronic nephritic syndrome	0.003	0.997	0.000
G82 Paraplegia and tetraplegia	0.000	0.997	0.003
I60.5 Subarachnoid haemorrhage from vertebral artery	0.000	0.997	0.003
S12.2 Fracture of other specified cervical vertebra	0.000	0.997	0.003
H69.9 Eustachian tube disorder, unspecified	0.003	0.997	0.000
E10 Insulin-dependent diabetes mellitus	0.000	0.997	0.003
G82.1 Spastic paraplegia	0.000	0.997	0.003
Q26 Congenital malformations of great veins	0.000	0.997	0.003
Q20 Congenital malformations of cardiac chambers and connexions	0.000	0.997	0.003
I42.8 Other cardiomyopathies	0.003	0.997	0.000
Q24.4 Congenital subaortic stenosis	0.000	0.997	0.003
Q24.3 Pulmonary infundibular stenosis	0.000	0.997	0.003
Q24.2 Cor triatriatum	0.000	0.997	0.003
Q24.1 Levocardia	0.000	0.997	0.003
E10.4 With neurological complications	0.000	0.997	0.003
Q24.6 Congenital heart block	0.000	0.997	0.003
I60.6 Subarachnoid haemorrhage from other intracranial arteries	0.000	0.997	0.003
Q24.8 Other specified congenital malformations of heart	0.000	0.997	0.003
Q22 Congenital malformations of pulmonary and tricuspid valves	0.000	0.997	0.003
N03.8 Other	0.003	0.997	0.000
N18.8 Other chronic renal failure	0.003	0.997	0.000
Q28 Other congenital malformations of circulatory system	0.000	0.997	0.003
I60.1 Subarachnoid haemorrhage from middle cerebral artery	0.000	0.997	0.003
Q87.4 Marfan's syndrome	0.003	0.997	0.000
E10.2 With renal complications	0.000	0.997	0.003
N03.5 Diffuse mesangiocapillary glomerulonephritis	0.003	0.997	0.000
Q24.0 Dextrocardia	0.000	0.997	0.003
L89.1 Stage II decubitus ulcer	0.000	0.997	0.003
I60.0 Subarachnoid haemorrhage from carotid siphon and bifurcation	0.000	0.997	0.003
H16 Keratitis	0.003	0.997	0.000
I80.0 Phlebitis and thrombophlebitis of superficial vessels of lower extremities	0.000	0.997	0.003
I60.7 Subarachnoid haemorrhage from intracranial artery, unspecified	0.000	0.997	0.003
K42.0 Umbilical hernia with obstruction, without gangrene	0.003	0.997	0.000
N41.0 Acute prostatitis	0.003	0.997	0.000
E10.8 With unspecified complications	0.000	0.997	0.003
N03.7 Diffuse crescentic glomerulonephritis	0.003	0.997	0.000
N03.6 Dense deposit disease	0.003	0.997	0.000
N03.4 Diffuse endocapillary proliferative glomerulonephritis	0.003	0.997	0.000
N03.3 Diffuse mesangial proliferative glomerulonephritis	0.003	0.997	0.000
N03.2 Diffuse membranous glomerulonephritis	0.003	0.997	0.000
N03.0 Minor glomerular abnormality	0.003	0.997	0.000
E10.6 With other specified complications	0.000	0.997	0.003
G82.3 Flaccid tetraplegia	0.000	0.997	0.003
G82.0 Flaccid paraplegia	0.000	0.997	0.003
E10.3 With ophthalmic complications	0.000	0.997	0.003
I42.9 Cardiomyopathy, unspecified	0.003	0.997	0.000
H16.3 Interstitial and deep keratitis	0.003	0.997	0.000
Q25 Congenital malformations of great arteries	0.000	0.997	0.003
N03.1 Focal and segmental glomerular lesions	0.003	0.997	0.000
N18.0 End-stage renal disease	0.003	0.997	0.000
S12.21 Fracture of other specified cervical vertebra (open)	0.000	0.997	0.002
H16.4 Corneal neovascularisation	0.003	0.997	0.000
Q28.2 Arteriovenous malformation of cerebral vessels	0.000	0.997	0.003
K56.0 Paralytic ileus	0.000	0.997	0.003
E10.5 With peripheral circulatory complications	0.000	0.997	0.003
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.000	0.997	0.002
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.000	0.997	0.002
Q20.6 Isomerism of atrial appendages	0.000	0.997	0.002
Q20.5 Discordant atrioventricular connexion	0.000	0.997	0.002
Q20.4 Double inlet ventricle	0.000	0.997	0.002
Q20.3 Discordant ventriculoarterial connexion	0.000	0.997	0.002
Q20.2 Double outlet left ventricle	0.000	0.997	0.002
Q20.1 Double outlet right ventricle	0.000	0.997	0.002
Q20.0 Common arterial trunk	0.000	0.997	0.002
Q26.9 Congenital malformation of great vein, unspecified	0.000	0.997	0.002
Q26.8 Other congenital malformations of great veins	0.000	0.997	0.002
Q26.6 Portal vein-hepatic artery fistula	0.000	0.997	0.002
Q26.5 Anomalous portal venous connexion	0.000	0.997	0.002
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.000	0.997	0.002
Q26.3 Partial anomalous pulmonary venous connexion	0.000	0.997	0.002
Q26.2 Total anomalous pulmonary venous connexion	0.000	0.997	0.002
Q26.1 Persistent left superior vena cava	0.000	0.997	0.002
Q26.0 Congenital stenosis of vena cava	0.000	0.997	0.002
E10.1 With ketoacidosis	0.000	0.997	0.003
Q23 Congenital malformations of aortic and mitral valves	0.000	0.997	0.002
K83.8 Other specified diseases of biliary tract	0.000	0.997	0.003
G45 Transient cerebral ischaemic attacks and related syndromes	0.003	0.997	0.000
I80.8 Phlebitis and thrombophlebitis of other sites	0.000	0.998	0.002
W21.9 Unspecified place	0.000	0.998	0.002
H16.0 Corneal ulcer	0.002	0.998	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.000	0.998	0.002
Q22.8 Other congenital malformations of tricuspid valve	0.000	0.998	0.002
Q22.6 Hypoplastic right heart syndrome	0.000	0.998	0.002
Q22.4 Congenital tricuspid stenosis	0.000	0.998	0.002
Q22.3 Other congenital malformations of pulmonary valve	0.000	0.998	0.002
Q22.2 Congenital pulmonary valve insufficiency	0.000	0.998	0.002
Q22.0 Pulmonary valve atresia	0.000	0.998	0.002
Q85.0 Neurofibromatosis (nonmalignant)	0.002	0.998	0.000
Q22.1 Congenital pulmonary valve stenosis	0.000	0.998	0.002
Q28.9 Congenital malformation of circulatory system, unspecified	0.000	0.998	0.002
Q28.8 Other specified congenital malformations of circulatory system	0.000	0.998	0.002
Q28.1 Other malformations of precerebral vessels	0.000	0.998	0.002
N64.1 Fat necrosis of breast	0.000	0.998	0.002
T78.4 Allergy, unspecified	0.000	0.998	0.002
I60.4 Subarachnoid haemorrhage from basilar artery	0.000	0.998	0.002
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
H80-H83 Diseases of inner ear	0.002	0.998	0.000
Q25.0 Patent ductus arteriosus	0.000	0.998	0.002
Q61.5 Medullary cystic kidney	0.002	0.998	0.000
Q22.5 Ebstein's anomaly	0.000	0.998	0.002
E10.0 With coma	0.000	0.998	0.002
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
G45.0 Vertebro-basilar artery syndrome	0.002	0.998	0.000
S12.70 Multiple fractures of cervical spine (closed)	0.000	0.998	0.002
E10.7 With multiple complications	0.000	0.998	0.002
Q82.5 Congenital nonneoplastic naevus	0.002	0.998	0.000
S42.4 Fracture of lower end of humerus	0.000	0.998	0.002
S12 Fracture of neck	0.000	0.998	0.002
C67.6 Ureteric orifice	0.000	0.998	0.002
H69.8 Other specified disorders of Eustachian tube	0.002	0.998	0.000
R84.5 Abnormal microbiological findings	0.002	0.998	0.000
H16.8 Other keratitis	0.002	0.998	0.000
K72.9 Hepatic failure, unspecified	0.002	0.998	0.000
S12.7 Multiple fractures of cervical spine	0.000	0.998	0.002
Q25.9 Congenital malformation of great arteries, unspecified	0.000	0.998	0.002
Q25.8 Other congenital malformations of great arteries	0.000	0.998	0.002
Q25.5 Atresia of pulmonary artery	0.000	0.998	0.002
Q25.3 Stenosis of aorta	0.000	0.998	0.002
Q25.2 Atresia of aorta	0.000	0.998	0.002
Q28.0 Arteriovenous malformation of precerebral vessels	0.000	0.998	0.002
Y89.9 Sequelae of unspecified external cause	0.002	0.998	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.000	0.998	0.002
Q28.3 Other malformations of cerebral vessels	0.000	0.998	0.002
H16.2 Keratoconjunctivitis	0.002	0.998	0.000
K46.9 Unspecified abdominal hernia without obstruction or gangrene	0.002	0.998	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.002	0.998	0.000
Q25.6 Stenosis of pulmonary artery	0.000	0.998	0.002
Q61.9 Cystic kidney disease, unspecified	0.002	0.998	0.000
H81.0 Meniere's disease	0.002	0.998	0.000
T82.2 Mechanical complication of coronary artery bypass and valve grafts	0.002	0.998	0.000
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.000	0.998	0.002
H69 Other disorders of Eustachian tube	0.002	0.998	0.000
G82.4 Spastic tetraplegia	0.000	0.998	0.002
G71.0 Muscular dystrophy	0.000	0.998	0.002
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.000	0.998	0.002
Q23.8 Other congenital malformations of aortic and mitral valves	0.000	0.998	0.002
Q23.4 Hypoplastic left heart syndrome	0.000	0.998	0.002
Q23.3 Congenital mitral insufficiency	0.000	0.998	0.002
Q23.2 Congenital mitral stenosis	0.000	0.998	0.002
C67.1 Dome of bladder	0.000	0.998	0.002
G45.2 Multiple and bilateral precerebral artery syndromes	0.002	0.998	0.000
H16.1 Other superficial keratitis without conjunctivitis	0.002	0.998	0.000
I62.9 Intracranial haemorrhage (nontraumatic), unspecified	0.002	0.998	0.000
R22.1 Localised swelling, mass and lump, neck	0.000	0.998	0.002
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.002	0.998	0.000
R90.8 Other abnormal findings on diagnostic imaging of central nervous system	0.000	0.998	0.002
S42.41 Fracture of lower end of humerus (open)	0.000	0.998	0.002
G45.1 Carotid artery syndrome (hemispheric)	0.002	0.998	0.000
G03.9 Meningitis, unspecified	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
N92.4 Excessive bleeding in the premenopausal period	0.000	0.998	0.002
L50.9 Urticaria, unspecified	0.000	0.998	0.002
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.002	0.998	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.002	0.998	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.002	0.998	0.000
H82 Vertiginous syndromes in diseases classified elsewhere	0.002	0.998	0.000
O20 Haemorrhage in early pregnancy	0.002	0.998	0.000
Q82 Other congenital malformations of skin	0.002	0.998	0.000
Q23.0 Congenital stenosis of aortic valve	0.000	0.998	0.002
Q25.4 Other congenital malformations of aorta	0.000	0.998	0.002
Q25.1 Coarctation of aorta	0.000	0.998	0.002
S12.0 Fracture of first cervical vertebra	0.000	0.998	0.002
I42.2 Other hypertrophic cardiomyopathy	0.002	0.998	0.000
Q85.1 Tuberous sclerosis	0.002	0.998	0.000
I42 Cardiomyopathy	0.002	0.998	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.002	0.998	0.000
S12.9 Fracture of neck, part unspecified	0.000	0.998	0.002
S12.8 Fracture of other parts of neck	0.000	0.998	0.002
S12.71 Multiple fractures of cervical spine (open)	0.000	0.998	0.002
G45.3 Amaurosis fugax	0.002	0.998	0.000
S66.1 Injury of flexor muscle and tendon of other finger at wrist and hand level	0.002	0.998	0.000
N02.8 Other	0.002	0.998	0.000
J84.1 Other interstitial pulmonary diseases with fibrosis	0.000	0.998	0.002
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.002	0.998	0.000
D76.2 Haemophagocytic syndrome, infection-associated	0.000	0.998	0.002
D76.1 Haemophagocytic lymphohistiocytosis	0.000	0.998	0.002
D76.0 Langerhans' cell histiocytosis, not elsewhere classified	0.000	0.998	0.002
M80.98 Unspecified osteoporosis with pathological fracture (Other)	0.002	0.998	0.000
H69.0 Patulous Eustachian tube	0.002	0.998	0.000
Z94.4 Liver transplant status	0.002	0.998	0.000
Q61 Cystic kidney disease	0.002	0.998	0.000
H21.5 Other adhesions and disruptions of iris and ciliary body	0.002	0.998	0.000
K80.2 Calculus of gallbladder without cholecystitis	0.002	0.998	0.000
Q85.9 Phakomatosis, unspecified	0.002	0.998	0.000
Q82.2 Mastocytosis	0.002	0.998	0.000
S64.0 Injury of ulnar nerve at wrist and hand level	0.002	0.998	0.000
H80 Otosclerosis	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
S12.00 Fracture of first cervical vertebra (closed)	0.000	0.998	0.002
C67.8 Overlapping lesion of bladder	0.000	0.998	0.002
C67.0 Trigone of bladder	0.000	0.998	0.002
Q82.9 Congenital malformation of skin, unspecified	0.002	0.998	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.002	0.998	0.000
Q82.3 Incontinentia pigmenti	0.002	0.998	0.000
Q82.1 Xeroderma pigmentosum	0.002	0.998	0.000
S12.1 Fracture of second cervical vertebra	0.000	0.998	0.002
C67 Malignant neoplasm of bladder	0.000	0.998	0.002
I80 Phlebitis and thrombophlebitis	0.000	0.998	0.002
M10.97 Gout, unspecified (Ankle and foot)	0.000	0.998	0.002
S12.01 Fracture of first cervical vertebra (open)	0.000	0.998	0.001
C02.1 Border of tongue	0.000	0.998	0.002
K76.7 Hepatorenal syndrome	0.002	0.998	0.000
M41.95 Scoliosis, unspecified (Thoracolumbar region)	0.002	0.998	0.000
I42.5 Other restrictive cardiomyopathy	0.002	0.998	0.000
I42.3 Endomyocardial (eosinophilic) disease	0.002	0.998	0.000
Q79.6 Ehlers-Danlos syndrome	0.002	0.998	0.000
S12.81 Fracture of other parts of neck (open)	0.000	0.998	0.001
S12.80 Fracture of other parts of neck (closed)	0.000	0.998	0.001
S12.91 Fracture of neck, part unspecified (open)	0.000	0.998	0.001
I42.4 Endocardial fibroelastosis	0.002	0.998	0.000
I62.0 Subdural haemorrhage (acute) (nontraumatic)	0.002	0.998	0.000
N02.1 Focal and segmental glomerular lesions	0.002	0.998	0.000
Q83 Congenital malformations of breast	0.002	0.998	0.000
C41.0 Bones of skull and face	0.002	0.998	0.000
O20.8 Other haemorrhage in early pregnancy	0.002	0.998	0.000
M41.94 Scoliosis, unspecified (Thoracic region)	0.002	0.998	0.000
S12.90 Fracture of neck, part unspecified (closed)	0.000	0.998	0.001
C67.3 Anterior wall of bladder	0.000	0.998	0.002
I42.1 Obstructive hypertrophic cardiomyopathy	0.002	0.998	0.000
N02 Recurrent and persistent haematuria	0.002	0.998	0.000
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
Z46.8 Fitting and adjustment of other specified devices	0.000	0.998	0.002
C15.9 Oesophagus, unspecified	0.000	0.998	0.002
Y43.1 Antineoplastic antimetabolites	0.002	0.998	0.000
J95.0 Tracheostomy malfunction	0.000	0.998	0.002
Q61.8 Other cystic kidney diseases	0.001	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.001	0.998	0.000
Q82.0 Hereditary lymphoedema	0.001	0.998	0.000
Q83.1 Accessory breast	0.001	0.998	0.000
Y95 Nosocomial condition	0.000	0.998	0.002
H80.8 Other otosclerosis	0.001	0.998	0.000
H80.2 Cochlear otosclerosis	0.001	0.998	0.000
H80.1 Otosclerosis involving oval window, obliterative	0.001	0.998	0.000
H80.0 Otosclerosis involving oval window, nonobliterative	0.001	0.998	0.000
I62.1 Nontraumatic extradural haemorrhage	0.001	0.998	0.000
Q61.4 Renal dysplasia	0.001	0.998	0.000
R93.4 Abnormal findings on diagnostic imaging of urinary organs	0.000	0.998	0.002
I80.9 Phlebitis and thrombophlebitis of unspecified site	0.000	0.998	0.001
M22.0 Recurrent dislocation of patella	0.001	0.998	0.000
Q35.9 Cleft palate, unspecified	0.001	0.998	0.000
Q80.9 Congenital ichthyosis, unspecified	0.001	0.998	0.000
Q80.8 Other congenital ichthyosis	0.001	0.998	0.000
Q80.4 Harlequin foetus	0.001	0.998	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.001	0.998	0.000
Q80.2 Lamellar ichthyosis	0.001	0.998	0.000
Q80.1 X-linked ichthyosis	0.001	0.998	0.000
Q80.0 Ichthyosis vulgaris	0.001	0.998	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.001	0.998	0.000
Q81.8 Other epidermolysis bullosa	0.001	0.998	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.001	0.998	0.000
Q81.1 Epidermolysis bullosa letalis	0.001	0.998	0.000
Q81.0 Epidermolysis bullosa simplex	0.001	0.998	0.000
Q84.9 Congenital malformation of integument, unspecified	0.001	0.998	0.000
Q84.8 Other specified congenital malformations of integument	0.001	0.998	0.000
Q84.6 Other congenital malformations of nails	0.001	0.998	0.000
Q84.5 Enlarged and hypertrophic nails	0.001	0.998	0.000
Q84.4 Congenital leukonychia	0.001	0.998	0.000
Q84.3 Anonychia	0.001	0.998	0.000
Q84.2 Other congenital malformations of hair	0.001	0.998	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.001	0.998	0.000
Q84.0 Congenital alopecia	0.001	0.998	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.001	0.998	0.000
Q86.2 Dysmorphism due to warfarin	0.001	0.998	0.000
Q86.1 Foetal hydantoin syndrome	0.001	0.998	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.001	0.998	0.000
I62 Other nontraumatic intracranial haemorrhage	0.002	0.998	0.000
M70.75 Other bursitis of hip-Pelvic/Thigh	0.000	0.998	0.001
S12.11 Fracture of second cervical vertebra (open)	0.000	0.998	0.001
C67.7 Urachus	0.000	0.998	0.001
I83.0 Varicose veins of lower extremities with ulcer	0.000	0.998	0.001
N02.0 Minor glomerular abnormality	0.001	0.998	0.000
S14.1 Other and unspecified injuries of cervical spinal cord	0.000	0.998	0.001
M22 Disorders of patella	0.002	0.998	0.000
L94.0 Localised scleroderma [morphea]	0.001	0.999	0.000
B91 Sequelae of poliomyelitis	0.001	0.999	0.000
N00-N08 Glomerular diseases	0.001	0.999	0.000
Z94.5 Skin transplant status	0.001	0.999	0.000
M41.92 Scoliosis, unspecified (Cervical region)	0.001	0.999	0.000
C74.9 Adrenal gland, unspecified	0.001	0.999	0.000
E24.2 Drug-induced Cushing's syndrome	0.001	0.999	0.000
G45.8 Other transient cerebral ischaemic attacks and related syndromes	0.001	0.999	0.000
I42.7 Cardiomyopathy due to drugs and other external agents	0.001	0.999	0.000
M54.6 Pain in thoracic spine	0.000	0.999	0.001
Q23.1 Congenital insufficiency of aortic valve	0.000	0.999	0.001
Q82.8 Other specified congenital malformations of skin	0.001	0.999	0.000
Q83.9 Congenital malformation of breast, unspecified	0.001	0.999	0.000
Q83.2 Absent nipple	0.001	0.999	0.000
Q83.0 Congenital absence of breast with absent nipple	0.001	0.999	0.000
B95.3 Streptococcus pneumoniae as the cause of diseases classified to other chapters	0.001	0.999	0.000
M92.7 Juvenile osteochondrosis of metatarsus	0.001	0.999	0.000
N02.7 Diffuse crescentic glomerulonephritis	0.001	0.999	0.000
N02.6 Dense deposit disease	0.001	0.999	0.000
N02.5 Diffuse mesangiocapillary glomerulonephritis	0.001	0.999	0.000
N02.4 Diffuse endocapillary proliferative glomerulonephritis	0.001	0.999	0.000
N02.3 Diffuse mesangial proliferative glomerulonephritis	0.001	0.999	0.000
W01.1 Residential institution	0.001	0.999	0.000
X68.9 Unspecified place	0.000	0.999	0.001
Q89 Other congenital malformations, not elsewhere classified	0.001	0.999	0.000
C67.4 Posterior wall of bladder	0.000	0.999	0.001
H58.8 Visual disturbances in diseases classified elsewhere	0.000	0.999	0.001
I80.3 Phlebitis and thrombophlebitis of lower extremities, unspecified	0.000	0.999	0.001
K75.0 Abscess of liver	0.000	0.999	0.001
L28.0 Lichen simplex chronicus	0.001	0.999	0.000
M41.9 Scoliosis, unspecified	0.001	0.999	0.000
C67.9 Bladder, unspecified	0.000	0.999	0.001
K61.3 Ischiorectal abscess	0.001	0.999	0.000
Q83.3 Accessory nipple	0.001	0.999	0.000
N00 Acute nephritic syndrome	0.001	0.999	0.000
M41.90 Scoliosis, unspecified (Multiple sites in spine)	0.001	0.999	0.000
S06.50 Traumatic subdural haemorrhage (without open intracranial wound)	0.000	0.999	0.001
S32.30 Fracture of ilium (closed)	0.001	0.999	0.000
L94.2 Calcinosis cutis	0.001	0.999	0.000
O12.1 Gestational proteinuria	0.000	0.999	0.001
O73.0 Retained placenta, without haemorrhage	0.001	0.999	0.000
M22.9 Disorder of patella, unspecified	0.001	0.999	0.000
M22.3 Other derangements of patella	0.001	0.999	0.000
N04.1 Focal and segmental glomerular lesions	0.001	0.999	0.000
C49.9 Connective and soft tissue, unspecified	0.001	0.999	0.000
L12.1 Cicatricial pemphigoid	0.000	0.999	0.001
M22.1 Recurrent subluxation of patella	0.001	0.999	0.000
Q54.9 Hypospadias, unspecified	0.001	0.999	0.000
H21 Other disorders of iris and ciliary body	0.001	0.999	0.000
H21.2 Degeneration of iris and ciliary body	0.001	0.999	0.000
N00.9 Unspecified	0.001	0.999	0.000
N02.2 Diffuse membranous glomerulonephritis	0.001	0.999	0.000
Y84.6 Urinary catheterisation	0.000	0.999	0.001
N07 Hereditary nephropathy, not elsewhere classified	0.001	0.999	0.000
N06 Isolated proteinuria with specified morphological lesion	0.001	0.999	0.000
N01 Rapidly progressive nephritic syndrome	0.001	0.999	0.000
Q35 Cleft palate	0.001	0.999	0.000
C41.4 Pelvic bones, sacrum and coccyx	0.001	0.999	0.000
C69.3 Choroid	0.000	0.999	0.001
H01.0 Blepharitis	0.000	0.999	0.001
Q54.1 Hypospadias, penile	0.001	0.999	0.000
Q89.3 Situs inversus	0.001	0.999	0.000
S51.8 Open wound of other parts of forearm	0.001	0.999	0.000
M54.69 Pain in thoracic spine-Site unspe	0.000	0.999	0.001
M54.68 Pain in thoracic spine-Sacral/sacrococ	0.000	0.999	0.001
M54.67 Pain in thoracic spine-Lumbosacral	0.000	0.999	0.001
M54.66 Pain in thoracic spine-Lumbar	0.000	0.999	0.001
M54.65 Pain in thoracic spine (Thoracolumbar region)	0.000	0.999	0.001
M54.62 Pain in thoracic spine-Cervical	0.000	0.999	0.001
M54.61 Pain in thoracic spine-Occipit-atl-axl	0.000	0.999	0.001
M54.60 Pain in thoracic spine (Multiple sites in spine)	0.000	0.999	0.001
I80.1 Phlebitis and thrombophlebitis of femoral vein	0.000	0.999	0.001
Q53.2 Undescended testicle, bilateral	0.001	0.999	0.000
Q89.9 Congenital malformation, unspecified	0.001	0.999	0.000
Q89.8 Other specified congenital malformations	0.001	0.999	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.001	0.999	0.000
Q89.4 Conjoined twins	0.001	0.999	0.000
Q89.1 Congenital malformations of adrenal gland	0.001	0.999	0.000
Q89.0 Congenital malformations of spleen	0.001	0.999	0.000
S13.6 Sprain and strain of joints and ligaments of other and unspecified parts of neck	0.000	0.999	0.001
M41.98 Scoliosis, unspecified (Sacral and sacrococcygeal region)	0.001	0.999	0.000
M41.97 Scoliosis, unspecified (Lumbosacral region)	0.001	0.999	0.000
M41.93 Scoliosis, unspecified (Cervicothoracic region)	0.001	0.999	0.000
M41.91 Scoliosis, unspecified (Occipito-atlanto-axial region)	0.001	0.999	0.000
E24.8 Other Cushing's syndrome	0.001	0.999	0.000
T78.2 Anaphylactic shock, unspecified	0.000	0.999	0.001
Y54.7 Agents affecting calcification	0.001	0.999	0.000
Z94.2 Lung transplant status	0.001	0.999	0.000
H18.6 Keratoconus	0.001	0.999	0.000
N00.8 Other	0.001	0.999	0.000
N00.7 Diffuse crescentic glomerulonephritis	0.001	0.999	0.000
N00.6 Dense deposit disease	0.001	0.999	0.000
N00.5 Diffuse mesangiocapillary glomerulonephritis	0.001	0.999	0.000
N00.4 Diffuse endocapillary proliferative glomerulonephritis	0.001	0.999	0.000
N00.3 Diffuse mesangial proliferative glomerulonephritis	0.001	0.999	0.000
N00.2 Diffuse membranous glomerulonephritis	0.001	0.999	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