TreeWAS – Variant ID: rs12704645

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
Z88.0 Personal history of allergy to penicillin	0.000	0.970	0.030
R22.1 Localised swelling, mass and lump, neck	0.000	0.988	0.012
K43.9 Ventral hernia without obstruction or gangrene	0.000	0.988	0.012
G40.6 Grand mal seizures, unspecified (with or without petit mal)	0.000	0.990	0.010
R09.8 Other specified symptoms and signs involving the circulatory and respiratory systems	0.010	0.990	0.000
E53.8 Deficiency of other specified B group vitamins	0.000	0.991	0.009
N03.9 Unspecified	0.009	0.991	0.000
B44.9 Aspergillosis, unspecified	0.000	0.992	0.008
B44.1 Other pulmonary aspergillosis	0.000	0.993	0.007
B44 Aspergillosis	0.000	0.994	0.006
Q27.3 Peripheral arteriovenous malformation	0.006	0.994	0.000
Q27 Other congenital malformations of peripheral vascular system	0.006	0.994	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.006	0.994	0.000
S92.00 Fracture of calcaneus (closed)	0.006	0.994	0.000
Q28 Other congenital malformations of circulatory system	0.005	0.995	0.000
Q24 Other congenital malformations of heart	0.005	0.995	0.000
Q28.2 Arteriovenous malformation of cerebral vessels	0.005	0.995	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.005	0.995	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.005	0.995	0.000
W07.0 Home	0.005	0.995	0.000
B44.7 Disseminated aspergillosis	0.000	0.995	0.005
B44.2 Tonsillar aspergillosis	0.000	0.995	0.005
B44.0 Invasive pulmonary aspergillosis	0.000	0.995	0.005
Q24.6 Congenital heart block	0.005	0.995	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.005	0.995	0.000
B44.8 Other forms of aspergillosis	0.000	0.995	0.005
Q27.4 Congenital phlebectasia	0.005	0.995	0.000
Q27.2 Other congenital malformations of renal artery	0.005	0.995	0.000
Q27.1 Congenital renal artery stenosis	0.005	0.995	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.005	0.995	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.004	0.995	0.000
G40 Epilepsy	0.000	0.996	0.004
C85.9 Non-Hodgkin's lymphoma, unspecified type	0.004	0.996	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.004	0.996	0.000
Q25 Congenital malformations of great arteries	0.004	0.996	0.000
K40.3 Unilateral or unspecified inguinal hernia, with obstruction, without gangrene	0.004	0.996	0.000
Q24.5 Malformation of coronary vessels	0.004	0.996	0.000
N03 Chronic nephritic syndrome	0.004	0.996	0.000
G40.2 Localisation-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures	0.000	0.996	0.004
D35.0 Adrenal gland	0.004	0.996	0.000
G40.5 Special epileptic syndromes	0.000	0.996	0.004
Q24.4 Congenital subaortic stenosis	0.004	0.996	0.000
Q24.3 Pulmonary infundibular stenosis	0.004	0.996	0.000
Q24.2 Cor triatriatum	0.004	0.996	0.000
Q24.1 Levocardia	0.004	0.996	0.000
Q24.0 Dextrocardia	0.004	0.996	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.004	0.996	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.004	0.996	0.000
Q28.1 Other malformations of precerebral vessels	0.004	0.996	0.000
Q26 Congenital malformations of great veins	0.004	0.996	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.004	0.996	0.000
Q24.8 Other specified congenital malformations of heart	0.004	0.996	0.000
Q28.3 Other malformations of cerebral vessels	0.004	0.996	0.000
G40.0 Localisation-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localised onset	0.000	0.996	0.004
K43 Ventral hernia	0.000	0.996	0.004
E53 Deficiency of other B group vitamins	0.001	0.996	0.003
Q25.6 Stenosis of pulmonary artery	0.004	0.996	0.000
M65.91 Synovitis and tenosynovitis, unspecified (Shoulder region)	0.004	0.996	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.004	0.996	0.000
W07 Fall involving chair	0.004	0.996	0.000
B18.1 Chronic viral hepatitis B without delta-agent	0.000	0.996	0.004
G40.3 Generalised idiopathic epilepsy and epileptic syndromes	0.000	0.996	0.004
Q22.1 Congenital pulmonary valve stenosis	0.004	0.996	0.000
Q63.0 Accessory kidney	0.000	0.996	0.004
G40.7 Petit mal, unspecified, without grand mal seizures	0.000	0.996	0.004
Q23 Congenital malformations of aortic and mitral valves	0.004	0.996	0.000
N18.4 Chronic kidney disease, stage 4	0.000	0.996	0.004
D03.6 Melanoma in situ of upper limb, including shoulder	0.004	0.996	0.000
Q25.1 Coarctation of aorta	0.003	0.997	0.000
K04.6 Periapical abscess with sinus	0.003	0.997	0.000
W07.5 Trade and service area	0.003	0.997	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.003	0.997	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.003	0.997	0.000
Q22.6 Hypoplastic right heart syndrome	0.003	0.997	0.000
Q22.4 Congenital tricuspid stenosis	0.003	0.997	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.003	0.997	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.003	0.997	0.000
Q22.0 Pulmonary valve atresia	0.003	0.997	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.003	0.997	0.000
Q25.8 Other congenital malformations of great arteries	0.003	0.997	0.000
Q25.5 Atresia of pulmonary artery	0.003	0.997	0.000
Q25.3 Stenosis of aorta	0.003	0.997	0.000
Q25.2 Atresia of aorta	0.003	0.997	0.000
N03.8 Other	0.003	0.997	0.000
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
Q61.2 Polycystic kidney, adult type	0.000	0.997	0.003
N03.1 Focal and segmental glomerular lesions	0.003	0.997	0.000
Q22.5 Ebstein's anomaly	0.003	0.997	0.000
Q61.0 Congenital single renal cyst	0.000	0.997	0.003
S92.0 Fracture of calcaneus	0.003	0.997	0.000
Q23.3 Congenital mitral insufficiency	0.003	0.997	0.000
G40.4 Other generalised epilepsy and epileptic syndromes	0.000	0.997	0.003
N42.2 Atrophy of prostate	0.000	0.997	0.003
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.003	0.997	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.003	0.997	0.000
Q20.6 Isomerism of atrial appendages	0.003	0.997	0.000
Q20.5 Discordant atrioventricular connexion	0.003	0.997	0.000
Q20.4 Double inlet ventricle	0.003	0.997	0.000
Q20.3 Discordant ventriculoarterial connexion	0.003	0.997	0.000
Q20.2 Double outlet left ventricle	0.003	0.997	0.000
Q20.1 Double outlet right ventricle	0.003	0.997	0.000
Q20.0 Common arterial trunk	0.003	0.997	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.003	0.997	0.000
Q26.8 Other congenital malformations of great veins	0.003	0.997	0.000
Q26.6 Portal vein-hepatic artery fistula	0.003	0.997	0.000
Q26.5 Anomalous portal venous connexion	0.003	0.997	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.003	0.997	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.003	0.997	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.003	0.997	0.000
Q26.1 Persistent left superior vena cava	0.003	0.997	0.000
Q26.0 Congenital stenosis of vena cava	0.003	0.997	0.000
C82.9 Follicular non-Hodgkin's lymphoma, unspecified	0.003	0.997	0.000
R22 Localised swelling, mass and lump of skin and subcutaneous tissue	0.000	0.997	0.003
N03.5 Diffuse mesangiocapillary glomerulonephritis	0.003	0.997	0.000
Q25.0 Patent ductus arteriosus	0.003	0.997	0.000
W07.9 Unspecified place	0.003	0.997	0.000
C73 Malignant neoplasm of thyroid gland	0.000	0.997	0.003
R41.8 Other and unspecified symptoms and signs involving cognitive functions and awareness	0.000	0.997	0.003
Q61 Cystic kidney disease	0.000	0.997	0.003
E53.1 Pyridoxine deficiency	0.001	0.997	0.002
E53.0 Riboflavin deficiency	0.001	0.997	0.002
K43.7 Other and unspecified ventral hernia with gangrene	0.000	0.997	0.003
K43.6 Other and unspecified ventral hernia with obstruction, without gangrene	0.000	0.997	0.003
K43.5 Parastomal hernia without obstruction or gangrene	0.000	0.997	0.003
K43.4 Parastomal hernia with gangrene	0.000	0.997	0.003
K43.3 Parastomal hernia with obstruction, without gangrene	0.000	0.997	0.003
K43.2 Incisional hernia without obstruction or gangrene	0.000	0.997	0.003
K43.1 Ventral hernia with gangrene	0.000	0.997	0.003
R22.7 Localised swelling, mass and lump, multiple sites	0.000	0.997	0.003
G40.8 Other epilepsy	0.000	0.997	0.003
H35.9 Retinal disorder, unspecified	0.000	0.997	0.003
W07.2 School, other institution and public administrative area	0.003	0.997	0.000
W07.8 Other specified place	0.003	0.997	0.000
W07.7 Farm	0.003	0.997	0.000
W07.6 Industrial and construction area	0.003	0.997	0.000
W07.4 Street and highway	0.003	0.997	0.000
W07.3 Sports and athletics area	0.003	0.997	0.000
W07.1 Residential institution	0.003	0.997	0.000
H93.1 Tinnitus	0.003	0.997	0.000
W10.4 Street and highway	0.003	0.997	0.000
Q63 Other congenital malformations of kidney	0.000	0.997	0.003
T79.3 Post-traumatic wound infection, not elsewhere classified	0.003	0.997	0.000
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
Q23.2 Congenital mitral stenosis	0.003	0.997	0.000
Q23.0 Congenital stenosis of aortic valve	0.003	0.997	0.000
K86.0 Alcohol-induced chronic pancreatitis	0.000	0.997	0.003
Q21 Congenital malformations of cardiac septa	0.003	0.997	0.000
R22.9 Localised swelling, mass and lump, unspecified	0.000	0.997	0.003
R22.3 Localised swelling, mass and lump, upper limb	0.000	0.997	0.003
Q25.4 Other congenital malformations of aorta	0.002	0.997	0.000
G62.9 Polyneuropathy, unspecified	0.000	0.997	0.003
T79.6 Traumatic ischaemia of muscle	0.003	0.997	0.000
Q61.3 Polycystic kidney, unspecified	0.000	0.997	0.003
E61.1 Iron deficiency	0.003	0.997	0.000
S92.01 Fracture of calcaneus (open)	0.002	0.997	0.000
E53.9 Vitamin B deficiency, unspecified	0.001	0.997	0.002
T46.4 Angiotensin-converting-enzyme inhibitors	0.000	0.997	0.003
Q60-Q64 Congenital malformations of the urinary system	0.000	0.997	0.002
Q21.9 Congenital malformation of cardiac septum, unspecified	0.003	0.997	0.000
R57.2 Septic shock	0.000	0.997	0.003
Q63.2 Ectopic kidney	0.000	0.997	0.002
T46.1 Calcium-channel blockers	0.000	0.997	0.003
B18 Chronic viral hepatitis	0.000	0.997	0.003
G40.1 Localisation-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures	0.000	0.997	0.002
Q96.9 Turner's syndrome, unspecified	0.002	0.997	0.000
C82 Follicular [nodular] non-Hodgkin's lymphoma	0.003	0.997	0.000
T46.5 Other antihypertensive drugs, not elsewhere classified	0.000	0.997	0.002
Q61.8 Other cystic kidney diseases	0.000	0.998	0.002
Q61.1 Polycystic kidney, infantile type	0.000	0.998	0.002
Q18.1 Preauricular sinus and cyst	0.002	0.998	0.000
Q18.0 Sinus, fistula and cyst of branchial cleft	0.002	0.998	0.000
D17.9 Benign lipomatous neoplasm, unspecified	0.000	0.998	0.002
W07.29 Fall involving chair; School, other institution and public administrative area; During unspecified activity	0.002	0.998	0.000
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.000	0.998	0.002
W18.3 Sports and athletics area	0.002	0.998	0.000
M47.90 Spondylosis, unspecified (Multiple sites in spine)	0.000	0.998	0.002
H58.8 Visual disturbances in diseases classified elsewhere	0.002	0.998	0.000
N04.9 Unspecified	0.002	0.998	0.000
B18.2 Chronic viral hepatitis C	0.000	0.998	0.002
C82.3 Follicular lymphoma grade IIIa	0.002	0.998	0.000
K43.0 Ventral hernia with obstruction, without gangrene	0.000	0.998	0.002
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
Q21.2 Atrioventricular septal defect	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.000	0.998	0.002
C85 Other and unspecified types of non-Hodgkin's lymphoma	0.002	0.998	0.000
C82.7 Other types of follicular non-Hodgkin's lymphoma	0.002	0.998	0.000
T18.1 Foreign body in oesophagus	0.000	0.998	0.002
T46 Poisoning by agents primarily affecting the cardiovascular system	0.000	0.998	0.002
Q64 Other congenital malformations of urinary system	0.000	0.998	0.002
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.000	0.998	0.002
K12.0 Recurrent oral aphthae	0.002	0.998	0.000
E61 Deficiency of other nutrient elements	0.002	0.998	0.000
T79 Certain early complications of trauma, not elsewhere classified	0.002	0.998	0.000
S93.1 Dislocation of toe(s)	0.002	0.998	0.000
R57.0 Cardiogenic shock	0.000	0.998	0.002
Q61.4 Renal dysplasia	0.000	0.998	0.002
Q63.1 Lobulated, fused and horseshoe kidney	0.000	0.998	0.002
K86.2 Cyst of pancreas	0.000	0.998	0.002
Q61.9 Cystic kidney disease, unspecified	0.000	0.998	0.002
B18.8 Other chronic viral hepatitis	0.000	0.998	0.002
B18.0 Chronic viral hepatitis B with delta-agent	0.000	0.998	0.002
D07.2 Vagina	0.002	0.998	0.000
C92.0 Acute myeloid leukaemia	0.002	0.998	0.000
Q96 Turner's syndrome	0.002	0.998	0.000
C82.6 Cutaneous follicle centre lymphoma	0.002	0.998	0.000
C82.5 Diffuse follicle centre lymphoma	0.002	0.998	0.000
D04.3 Skin of other and unspecified parts of face	0.002	0.998	0.000
N04 Nephrotic syndrome	0.002	0.998	0.000
B18.9 Chronic viral hepatitis, unspecified	0.000	0.998	0.002
C82.1 Mixed small cleaved and large cell, follicular	0.002	0.998	0.000
N04.1 Focal and segmental glomerular lesions	0.002	0.998	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.000	0.998	0.002
S02.20 Fracture of nasal bones (closed)	0.002	0.998	0.000
Q61.5 Medullary cystic kidney	0.000	0.998	0.002
T79.4 Traumatic shock	0.002	0.998	0.000
C84.0 Mycosis fungoides	0.002	0.998	0.000
D06.9 Cervix, unspecified	0.002	0.998	0.000
K75.0 Abscess of liver	0.002	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.000	0.998	0.002
W10 Fall on and from stairs and steps	0.002	0.998	0.000
D46.2 Refractory anaemia with excess of blasts	0.002	0.998	0.000
Q18.9 Congenital malformation of face and neck, unspecified	0.002	0.998	0.000
Q18.8 Other specified congenital malformations of face and neck	0.002	0.998	0.000
Q18.7 Microcheilia	0.002	0.998	0.000
Q18.6 Macrocheilia	0.002	0.998	0.000
Q18.5 Microstomia	0.002	0.998	0.000
Q18.4 Macrostomia	0.002	0.998	0.000
Q18.3 Webbing of neck	0.002	0.998	0.000
Q18.2 Other branchial cleft malformations	0.002	0.998	0.000
R57 Shock, not elsewhere classified	0.000	0.998	0.002
N64.1 Fat necrosis of breast	0.002	0.998	0.000
Q60.2 Renal agenesis, unspecified	0.000	0.998	0.002
C84 Peripheral and cutaneous T-cell lymphomas	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
C82.2 Large cell, follicular	0.002	0.998	0.000
Q62.5 Duplication of ureter	0.000	0.998	0.002
Q64.7 Other congenital malformations of bladder and urethra	0.000	0.998	0.002
R50.8 Other specified fever	0.002	0.998	0.000
R57.1 Hypovolaemic shock	0.000	0.998	0.002
C86.5 Angioimmunoblastic T-cell lymphoma	0.002	0.998	0.000
D07.1 Vulva	0.002	0.998	0.000
Q21.1 Atrial septal defect	0.002	0.998	0.000
D03 Melanoma in situ	0.002	0.998	0.000
M21.67 Other acquired deformities of ankle and foot-Ankle/foot	0.000	0.998	0.002
C85.2 Mediastinal (thymic) large B-cell lymphoma	0.002	0.998	0.000
N04.0 Minor glomerular abnormality	0.002	0.998	0.000
T79.8 Other early complications of trauma	0.002	0.998	0.000
C85.0 Lymphosarcoma	0.002	0.998	0.000
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.000	0.998	0.002
W11.6 Industrial and construction area	0.002	0.998	0.000
C92 Myeloid leukaemia	0.002	0.998	0.000
D07 Carcinoma in situ of other and unspecified genital organs	0.002	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
E61.2 Magnesium deficiency	0.002	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.000	0.998	0.002
Q64.8 Other specified congenital malformations of urinary system	0.000	0.998	0.002
Q64.6 Congenital diverticulum of bladder	0.000	0.998	0.002
Q64.5 Congenital absence of bladder and urethra	0.000	0.998	0.002
Q64.4 Malformation of urachus	0.000	0.998	0.002
Q64.2 Congenital posterior urethral valves	0.000	0.998	0.002
Q64.1 Exstrophy of urinary bladder	0.000	0.998	0.002
Q64.0 Epispadias	0.000	0.998	0.002
S81.8 Open wound of other parts of lower leg	0.002	0.998	0.000
T46.8 Antivaricose drugs, including sclerosing agents	0.000	0.998	0.002
T46.7 Peripheral vasodilators	0.000	0.998	0.002
T46.2 Other antidysrhythmic drugs, not elsewhere classified	0.000	0.998	0.002
Q17 Other congenital malformations of ear	0.002	0.998	0.000
C84.8 Cutaneous T-cell lymphoma, unspecified	0.002	0.998	0.000
C91.1 Chronic lymphocytic leukaemia	0.002	0.998	0.000
D21.1 Connective and other soft tissue of upper limb, including shoulder	0.000	0.998	0.002
Q11.1 Other anophthalmos	0.002	0.998	0.000
Q62.8 Other congenital malformations of ureter	0.000	0.998	0.002
Q62.7 Congenital vesico-uretero-renal reflux	0.000	0.998	0.002
Q62.6 Malposition of ureter	0.000	0.998	0.002
Q62.4 Agenesis of ureter	0.000	0.998	0.002
Q62.3 Other obstructive defects of renal pelvis and ureter	0.000	0.998	0.002
Q62.1 Atresia and stenosis of ureter	0.000	0.998	0.002
Q62.0 Congenital hydronephrosis	0.000	0.998	0.002
T46.6 Antihyperlipidaemic and antiarteriosclerotic drugs	0.000	0.998	0.002
C86 Other specified types of T/NK-cell lymphoma	0.002	0.998	0.000
S02.90 Fracture of skull and facial bones, part unspecified (closed)	0.002	0.998	0.000
F02.3 Dementia in Parkinson's disease	0.000	0.998	0.002
T46.0 Cardiac-stimulant glycosides and drugs of similar action	0.000	0.998	0.002
C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue	0.002	0.998	0.000
E61.9 Deficiency of nutrient element, unspecified	0.002	0.998	0.000
E61.8 Deficiency of other specified nutrient elements	0.002	0.998	0.000
E61.7 Deficiency of multiple nutrient elements	0.002	0.998	0.000
E61.6 Vanadium deficiency	0.002	0.998	0.000
E61.5 Molybdenum deficiency	0.002	0.998	0.000
E61.4 Chromium deficiency	0.002	0.998	0.000
E61.3 Manganese deficiency	0.002	0.998	0.000
E61.0 Copper deficiency	0.002	0.998	0.000
Q17.5 Prominent ear	0.002	0.998	0.000
S51.0 Open wound of elbow	0.002	0.998	0.000
T79.9 Unspecified early complication of trauma	0.002	0.998	0.000
T79.2 Traumatic secondary and recurrent haemorrhage	0.002	0.998	0.000
T79.1 Fat embolism (traumatic)	0.002	0.998	0.000
T79.0 Air embolism (traumatic)	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
C82.4 Follicular lymphoma grade IIIb	0.002	0.998	0.000
C82.0 Small cleaved cell, follicular	0.002	0.998	0.000
C92.1 Chronic myeloid leukaemia	0.002	0.998	0.000
D46.9 Myelodysplastic syndrome, unspecified	0.002	0.998	0.000
Q62.2 Congenital megaloureter	0.000	0.998	0.002
K86 Other diseases of pancreas	0.000	0.998	0.002
W18 Other fall on same level	0.002	0.998	0.000
D07.5 Prostate	0.002	0.998	0.000
R04.2 Haemoptysis	0.000	0.998	0.002
Q14 Congenital malformations of posterior segment of eye	0.002	0.998	0.000
W11 Fall on and from ladder	0.002	0.998	0.000
D03.2 Melanoma in situ of ear and external auricular canal	0.002	0.998	0.000
T46.3 Coronary vasodilators, not elsewhere classified	0.000	0.998	0.002
W10.1 Residential institution	0.002	0.998	0.000
Z30.5 Surveillance of (intra-uterine) contraceptive device	0.002	0.998	0.000
C78.1 Secondary malignant neoplasm of mediastinum	0.002	0.998	0.000
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified	0.002	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.002	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.002	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.002	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.002	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.002	0.998	0.000
Q96.0 Karyotype 45,X	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
X63.0 Home	0.000	0.998	0.002
N04.8 Other	0.002	0.998	0.000
N04.7 Diffuse crescentic glomerulonephritis	0.002	0.998	0.000
N04.6 Dense deposit disease	0.002	0.998	0.000
N04.5 Diffuse mesangiocapillary glomerulonephritis	0.002	0.998	0.000
N04.4 Diffuse endocapillary proliferative glomerulonephritis	0.002	0.998	0.000
N04.3 Diffuse mesangial proliferative glomerulonephritis	0.002	0.998	0.000
N04.2 Diffuse membranous glomerulonephritis	0.002	0.998	0.000
E50-E64 Other nutritional deficiencies	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
R50.0 Fever with chills	0.000	0.998	0.002
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
B37.1 Pulmonary candidiasis	0.000	0.998	0.002
D03.8 Melanoma in situ of other sites	0.002	0.998	0.000
E55.9 Vitamin D deficiency, unspecified	0.002	0.998	0.000
H43.1 Vitreous haemorrhage	0.000	0.998	0.002
I84.0 Internal thrombosed haemorrhoids	0.000	0.998	0.002
Q60.6 Potter's syndrome	0.000	0.998	0.001
Q60.5 Renal hypoplasia, unspecified	0.000	0.998	0.001
Q60.4 Renal hypoplasia, bilateral	0.000	0.998	0.001
Q60.1 Renal agenesis, bilateral	0.000	0.998	0.001
R52.1 Chronic intractable pain	0.002	0.998	0.000
W10.9 Unspecified place	0.002	0.998	0.000
W10.5 Trade and service area	0.002	0.998	0.000
W10.2 School, other institution and public administrative area	0.002	0.998	0.000
W10.0 Home	0.002	0.998	0.000
W10.7 Farm	0.002	0.998	0.000
E55 Vitamin D deficiency	0.002	0.998	0.000
S92.51 Fracture of other toe (open)	0.002	0.998	0.000
K86.8 Other specified diseases of pancreas	0.000	0.998	0.002
Q14.1 Congenital malformation of retina	0.002	0.998	0.000
R57.8 Other shock	0.000	0.998	0.002
W11.2 School, other institution and public administrative area	0.002	0.998	0.000
Q13 Congenital malformations of anterior segment of eye	0.002	0.998	0.000
C84.9 Mature T/NK-cell lymphoma, unspecified	0.002	0.998	0.000
C84.7 Anaplastic large cell lymphoma, ALK-negative	0.002	0.998	0.000
C84.6 Anaplastic large cell lymphoma, ALK-positive	0.002	0.998	0.000
C84.3 Lymphoepithelioid lymphoma	0.002	0.998	0.000
C84.2 T-zone lymphoma	0.002	0.998	0.000
C84.1 Sezary's diease	0.002	0.998	0.000
R57.9 Shock, unspecified	0.000	0.998	0.002
T46.9 Other and unspecified agents primarily affecting the cardiovascular system	0.000	0.998	0.001
D35 Benign neoplasm of other and unspecified endocrine glands	0.002	0.998	0.000
E58 Dietary calcium deficiency	0.002	0.998	0.000
Q15 Other congenital malformations of eye	0.002	0.998	0.000
W00-W19 Falls	0.002	0.998	0.000
C84.4 Peripheral T-cell lymphoma	0.002	0.998	0.000
E63 Other nutritional deficiencies	0.002	0.998	0.000
D03.9 Melanoma in situ, unspecified	0.002	0.998	0.000
D03.0 Melanoma in situ of lip	0.002	0.998	0.000
D07.0 Endometrium	0.002	0.998	0.000
T18.0 Foreign body in mouth	0.000	0.998	0.002
T18 Foreign body in alimentary tract	0.000	0.998	0.002
S06.20 Diffuse brain injury (without open intracranial wound)	0.002	0.998	0.000
C92.8 Acute myeloid leukaemia with multilineage dysplasia	0.002	0.998	0.000
C92.6 Acute myeloid leukaemia with 11q23-abnormality	0.002	0.998	0.000
C92.5 Acute myelomonocytic leukaemia	0.002	0.998	0.000
C92.3 Myeloid sarcoma	0.002	0.998	0.000
C92.2 Subacute myeloid leukaemia	0.002	0.998	0.000
D07.6 Other and unspecified male genital organs	0.002	0.998	0.000
D07.3 Other and unspecified female genital organs	0.002	0.998	0.000
E63.9 Nutritional deficiency, unspecified	0.001	0.998	0.000
F02.8 Dementia in other specified diseases classified elsewhere	0.000	0.998	0.002
Q11.3 Macrophthalmos	0.001	0.998	0.000
Q11.2 Microphthalmos	0.001	0.998	0.000
Q11.0 Cystic eyeball	0.001	0.998	0.000
R22.2 Localised swelling, mass and lump, trunk	0.000	0.998	0.002
W10.3 Sports and athletics area	0.002	0.998	0.000
D06 Carcinoma in situ of cervix uteri	0.002	0.998	0.000
Q17.9 Congenital malformation of ear, unspecified	0.001	0.998	0.000
Q17.8 Other specified congenital malformations of ear	0.001	0.998	0.000
Q17.4 Misplaced ear	0.001	0.998	0.000
Q17.3 Other misshapen ear	0.001	0.998	0.000
Q17.2 Microtia	0.001	0.998	0.000
Q17.1 Macrotia	0.001	0.998	0.000
Q17.0 Accessory auricle	0.001	0.998	0.000
C94 Other leukaemias of specified cell type	0.002	0.998	0.000
C93 Monocytic leukaemia	0.002	0.998	0.000
E56 Other vitamin deficiencies	0.001	0.998	0.000
C86.6 Primary cutaneous CD30-positive T-cell proliferations	0.001	0.998	0.000
C86.4 Blastic NK-cell lymphoma	0.001	0.998	0.000
C86.3 Subcutaneous panniculitis-like T-cell lymphoma	0.001	0.998	0.000
C86.2 Enteropathy-type (intestinal) T-cell lymphoma	0.001	0.998	0.000
C86.1 Hepatosplenic T-cell lymphoma	0.001	0.998	0.000
C86.0 Extranodal NK/T-cell lymphoma, nasal type	0.001	0.998	0.000
R82.8 Abnormal findings on cytological and histological examination of urine	0.000	0.998	0.002
S92.5 Fracture of other toe	0.002	0.998	0.000
W10.6 Industrial and construction area	0.001	0.998	0.000
D46 Myelodysplastic syndromes	0.002	0.998	0.000
E51 Thiamine deficiency	0.001	0.998	0.000
B16.9 Acute hepatitis B without delta-agent and without hepatic coma	0.000	0.998	0.002
D03.3 Melanoma in situ of other and unspecified parts of face	0.002	0.998	0.000
Q16.5 Congenital malformation of inner ear	0.001	0.998	0.000
Q16.4 Other congenital malformations of middle ear	0.001	0.998	0.000
Q16.3 Congenital malformation of ear ossicles	0.001	0.998	0.000
Q16.2 Absence of eustachian tube	0.001	0.998	0.000
Q16.1 Congenital absence, atresia and stricture of auditory canal (external)	0.001	0.998	0.000
Q16.0 Congenital absence of (ear) auricle	0.001	0.998	0.000
C96 Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue	0.001	0.998	0.000
M13.98 Arthritis, unspecified (Other)	0.000	0.998	0.002
M25.77 Osteophyte (Ankle and foot)	0.000	0.998	0.002
S02.21 Fracture of nasal bones (open)	0.002	0.998	0.000
C84.5 Other and unspecified T-cell lymphomas	0.001	0.998	0.000
D46.7 Other myelodysplastic syndromes	0.002	0.998	0.000
D46.5 Refractory anaemia with multi-lineage dysplasia	0.002	0.998	0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.001	0.998	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.001	0.998	0.000
Q14.3 Congenital malformation of choroid	0.001	0.998	0.000
Q14.2 Congenital malformation of optic disk	0.001	0.998	0.000
Q14.0 Congenital malformation of vitreous humour	0.001	0.998	0.000
Q60.3 Renal hypoplasia, unilateral	0.000	0.998	0.001
T79.5 Traumatic anuria	0.001	0.998	0.000
W18.9 Unspecified place	0.001	0.998	0.000
W18.8 Other specified place	0.001	0.998	0.000
W18.4 Street and highway	0.001	0.998	0.000
W18.2 School, other institution and public administrative area	0.001	0.998	0.000
W18.0 Home	0.001	0.998	0.000
W18.7 Farm	0.001	0.998	0.000
W18.6 Industrial and construction area	0.001	0.998	0.000
W14 Fall from tree	0.002	0.998	0.000
C67.6 Ureteric orifice	0.000	0.998	0.002
D35.2 Pituitary gland	0.002	0.998	0.000
N83.8 Other noninflammatory disorders of ovary, Fallopian tube and broad ligament	0.002	0.998	0.000
S14.1 Other and unspecified injuries of cervical spinal cord	0.000	0.998	0.002
W11.9 Unspecified place	0.001	0.998	0.000
W11.8 Other specified place	0.001	0.998	0.000
W11.0 Home	0.001	0.998	0.000
W11.7 Farm	0.001	0.998	0.000
W11.4 Street and highway	0.001	0.998	0.000
W11.3 Sports and athletics area	0.001	0.998	0.000
W11.1 Residential institution	0.001	0.998	0.000
C91 Lymphoid leukaemia	0.002	0.998	0.000
E54 Ascorbic acid deficiency	0.001	0.998	0.000
S92.20 Fracture of other tarsal bone(s) (closed)	0.001	0.998	0.000
E56.1 Deficiency of vitamin K	0.001	0.998	0.000
K86.9 Disease of pancreas, unspecified	0.000	0.998	0.002
S92.2 Fracture of other tarsal bone(s)	0.001	0.998	0.000
V44.5 Driver injured in traffic accident	0.001	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.001	0.998	0.000
S92 Fracture of foot, except ankle	0.002	0.998	0.000
C92.7 Other myeloid leukaemia	0.001	0.998	0.000
C95.0 Acute leukaemia of unspecified cell type	0.001	0.998	0.000
Q21.0 Ventricular septal defect	0.001	0.998	0.000
S02.2 Fracture of nasal bones	0.002	0.998	0.000
T18.5 Foreign body in anus and rectum	0.000	0.998	0.001
W08.9 Unspecified place	0.001	0.998	0.000
C95 Leukaemia of unspecified cell type	0.001	0.998	0.000
E64 Sequelae of malnutrition and other nutritional deficiencies	0.001	0.998	0.000
E50 Vitamin A deficiency	0.001	0.998	0.000
E60 Dietary zinc deficiency	0.001	0.998	0.000
E59 Dietary selenium deficiency	0.001	0.998	0.000
E52 Niacin deficiency [pellagra]	0.001	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.001	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.001	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.001	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.001	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.001	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.001	0.998	0.000
W16 Diving or jumping into water causing injury other than drowning or submersion	0.001	0.998	0.000
E51.2 Wernicke's encephalopathy	0.001	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.001	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.001	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.001	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.001	0.998	0.000
Q98.5 Karyotype 47,XYY	0.001	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.001	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.001	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