TreeWAS – Variant ID: rs742090

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
E83.1 Disorders of iron metabolism	1.000	0.000	0.000
K90.0 Coeliac disease	0.000	0.000	1.000
I83.9 Varicose veins of lower extremities without ulcer or inflammation	0.918	0.082	0.000
K90 Intestinal malabsorption	0.000	0.112	0.888
K90.9 Intestinal malabsorption, unspecified	0.000	0.169	0.831
K90.4 Malabsorption due to intolerance, not elsewhere classified	0.000	0.203	0.797
K44.9 Diaphragmatic hernia without obstruction or gangrene	0.727	0.273	0.000
K40 Inguinal hernia	0.720	0.280	0.000
K44 Diaphragmatic hernia	0.720	0.280	0.000
K40-K46 Hernia	0.717	0.283	0.000
K40.9 Unilateral or unspecified inguinal hernia, without obstruction or gangrene	0.699	0.301	0.000
K41 Femoral hernia	0.693	0.307	0.000
K40.3 Unilateral or unspecified inguinal hernia, with obstruction, without gangrene	0.692	0.308	0.000
K40.2 Bilateral inguinal hernia, without obstruction or gangrene	0.668	0.332	0.000
K41.9 Unilateral or unspecified femoral hernia, without obstruction or gangrene	0.663	0.337	0.000
K90.3 Pancreatic steatorrhoea	0.000	0.363	0.637
K90.2 Blind loop syndrome, not elsewhere classified	0.000	0.363	0.637
K90.1 Tropical sprue	0.000	0.363	0.637
K43 Ventral hernia	0.635	0.365	0.000
K43.9 Ventral hernia without obstruction or gangrene	0.602	0.398	0.000
K90.8 Other intestinal malabsorption	0.000	0.400	0.600
K41.2 Bilateral femoral hernia, without obstruction or gangrene	0.556	0.444	0.000
K41.4 Unilateral or unspecified femoral hernia, with gangrene	0.518	0.482	0.000
K40.1 Bilateral inguinal hernia, with gangrene	0.517	0.483	0.000
K41.3 Unilateral or unspecified femoral hernia, with obstruction, without gangrene	0.513	0.487	0.000
K41.1 Bilateral femoral hernia, with gangrene	0.497	0.503	0.000
K41.0 Bilateral femoral hernia, with obstruction, without gangrene	0.497	0.503	0.000
K44.1 Diaphragmatic hernia with gangrene	0.497	0.503	0.000
K44.0 Diaphragmatic hernia with obstruction, without gangrene	0.487	0.513	0.000
K43.1 Ventral hernia with gangrene	0.474	0.526	0.000
K40.4 Unilateral or unspecified inguinal hernia, with gangrene	0.456	0.544	0.000
K43.7 Other and unspecified ventral hernia with gangrene	0.455	0.545	0.000
K43.6 Other and unspecified ventral hernia with obstruction, without gangrene	0.455	0.545	0.000
K43.5 Parastomal hernia without obstruction or gangrene	0.455	0.545	0.000
K43.4 Parastomal hernia with gangrene	0.455	0.545	0.000
K43.3 Parastomal hernia with obstruction, without gangrene	0.455	0.545	0.000
K43.2 Incisional hernia without obstruction or gangrene	0.455	0.545	0.000
K40.0 Bilateral inguinal hernia, with obstruction, without gangrene	0.434	0.566	0.000
K45 Other abdominal hernia	0.363	0.637	0.000
K46 Unspecified abdominal hernia	0.301	0.698	0.000
K43.0 Ventral hernia with obstruction, without gangrene	0.276	0.724	0.000
K45.1 Other specified abdominal hernia with gangrene	0.260	0.740	0.000
K46.1 Unspecified abdominal hernia with gangrene	0.216	0.783	0.000
K45.8 Other specified abdominal hernia without obstruction or gangrene	0.206	0.793	0.000
K46.0 Unspecified abdominal hernia with obstruction, without gangrene	0.200	0.799	0.000
K45.0 Other specified abdominal hernia with obstruction, without gangrene	0.195	0.804	0.001
K42 Umbilical hernia	0.194	0.806	0.000
I83 Varicose veins of lower extremities	0.184	0.816	0.000
K42.1 Umbilical hernia with gangrene	0.134	0.866	0.000
I83.0 Varicose veins of lower extremities with ulcer	0.130	0.870	0.000
I83.1 Varicose veins of lower extremities with inflammation	0.102	0.898	0.000
I83.2 Varicose veins of lower extremities with both ulcer and inflammation	0.091	0.909	0.000
K42.0 Umbilical hernia with obstruction, without gangrene	0.070	0.930	0.000
E83 Disorders of mineral metabolism	0.070	0.930	0.000
B97.8 Other viral agents as the cause of diseases classified to other chapters	0.062	0.938	0.000
E83.9 Disorder of mineral metabolism, unspecified	0.058	0.942	0.000
K90-K93 Other diseases of the digestive system	0.000	0.946	0.054
K46.9 Unspecified abdominal hernia without obstruction or gangrene	0.050	0.949	0.001
E83.8 Other disorders of mineral metabolism	0.050	0.950	0.000
E83.2 Disorders of zinc metabolism	0.050	0.950	0.000
E83.0 Disorders of copper metabolism	0.050	0.950	0.000
K42.9 Umbilical hernia without obstruction or gangrene	0.041	0.959	0.000
E83.3 Disorders of phosphorus metabolism	0.041	0.959	0.000
K93 Disorders of other digestive organs in diseases classified elsewhere	0.000	0.961	0.039
D68.3 Haemorrhagic disorder due to circulating anticoagulants	0.039	0.961	0.000
D68 Other coagulation defects	0.037	0.963	0.000
D68.9 Coagulation defect, unspecified	0.036	0.964	0.000
D68.2 Hereditary deficiency of other clotting factors	0.034	0.966	0.000
D68.1 Hereditary factor XI deficiency	0.030	0.970	0.000
D68.6 Other Thrombophilia	0.029	0.971	0.000
D68.4 Acquired coagulation factor deficiency	0.028	0.972	0.000
K93.8 Disorders of other specified digestive organs in diseases classified elsewhere	0.000	0.972	0.028
K93.1 Megacolon in Chagas' disease	0.000	0.972	0.028
K93.0 Tuberculous disorders of intestines, peritoneum and mesenteric glands	0.000	0.972	0.028
D68.0 Von Willebrand's disease	0.026	0.974	0.000
D68.5 Primary Thrombophilia	0.024	0.976	0.000
D68.8 Other specified coagulation defects	0.018	0.982	0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.018	0.982	0.000
H34.8 Other retinal vascular occlusions	0.000	0.982	0.018
D66 Hereditary factor VIII deficiency	0.017	0.983	0.000
N05.9 Unspecified	0.000	0.984	0.016
B97 Viral agents as the cause of diseases classified to other chapters	0.016	0.984	0.000
H53.1 Subjective visual disturbances	0.000	0.985	0.015
R41.3 Other amnesia	0.000	0.985	0.015
D67 Hereditary factor IX deficiency	0.014	0.986	0.000
N05 Unspecified nephritic syndrome	0.000	0.986	0.014
R41 Other symptoms and signs involving cognitive functions and awareness	0.000	0.986	0.014
R41.2 Retrograde amnesia	0.000	0.986	0.014
H34 Retinal vascular occlusions	0.000	0.987	0.013
R41.8 Other and unspecified symptoms and signs involving cognitive functions and awareness	0.000	0.987	0.013
O36.8 Maternal care for other specified foetal problems	0.000	0.987	0.013
N05.1 Focal and segmental glomerular lesions	0.000	0.988	0.012
B97.4 Respiratory synctial virus as the cause of diseases classified to other chapters	0.012	0.988	0.000
H34.1 Central retinal artery occlusion	0.000	0.988	0.012
B97.6 Parvovirus as the cause of diseases classified to other chapters	0.012	0.988	0.000
B97.5 Reovirus as the cause of diseases classified to other chapters	0.012	0.988	0.000
B97.3 Retrovirus as the cause of diseases classified to other chapters	0.012	0.988	0.000
B97.2 Coronavirus as the cause of diseases classified to other chapters	0.012	0.988	0.000
B97.0 Adenovirus as the cause of diseases classified to other chapters	0.012	0.988	0.000
N05.8 Other	0.000	0.988	0.012
N05.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.988	0.011
H34.2 Other retinal artery occlusions	0.000	0.988	0.012
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.011	0.989	0.000
B97.1 Enterovirus as the cause of diseases classified to other chapters	0.011	0.989	0.000
R41.1 Anterograde amnesia	0.000	0.989	0.011
N05.2 Diffuse membranous glomerulonephritis	0.000	0.989	0.011
H34.9 Retinal vascular occlusion, unspecified	0.000	0.989	0.011
N05.6 Dense deposit disease	0.000	0.990	0.010
N05.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.990	0.010
N05.0 Minor glomerular abnormality	0.000	0.990	0.010
H34.0 Transient retinal artery occlusion	0.000	0.990	0.010
N05.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.990	0.010
I60.9 Subarachnoid haemorrhage, unspecified	0.000	0.991	0.009
E80.4 Gilbert's syndrome	0.009	0.991	0.000
N05.7 Diffuse crescentic glomerulonephritis	0.000	0.992	0.008
O36 Maternal care for other known or suspected foetal problems	0.000	0.992	0.008
N45.9 Orchitis, epididymitis and epididymo-orchitis without abscess	0.007	0.993	0.000
E80 Disorders of porphyrin and bilirubin metabolism	0.007	0.993	0.000
D22.4 Melanocytic naevi of scalp and neck	0.000	0.993	0.007
O36.6 Maternal care for excessive foetal growth	0.000	0.993	0.007
B97.7 Papillomavirus as the cause of diseases classified to other chapters	0.007	0.993	0.000
R31 Unspecified haematuria	0.007	0.993	0.000
E83.4 Disorders of magnesium metabolism	0.006	0.993	0.001
O36.9 Maternal care for foetal problem, unspecified	0.000	0.993	0.007
E80.1 Porphyria cutanea tarda	0.007	0.993	0.000
E80.2 Other porphyria	0.006	0.994	0.000
G24 Dystonia	0.006	0.994	0.000
O36.0 Maternal care for rhesus isoimmunisation	0.000	0.994	0.006
G24.5 Blepharospasm	0.006	0.994	0.000
O36.4 Maternal care for intra-uterine death	0.000	0.994	0.006
G24.8 Other dystonia	0.006	0.994	0.000
O36.7 Maternal care for viable foetus in abdominal pregnancy	0.000	0.994	0.006
O36.2 Maternal care for hydrops foetalis	0.000	0.994	0.006
H53 Visual disturbances	0.000	0.994	0.006
O36.1 Maternal care for other isoimmunisation	0.000	0.994	0.006
G24.9 Dystonia, unspecified	0.006	0.994	0.000
H53.9 Visual disturbance, unspecified	0.000	0.994	0.006
E80.7 Disorder of bilirubin metabolism, unspecified	0.005	0.994	0.000
E80.5 Crigler-Najjar syndrome	0.005	0.994	0.000
E80.3 Defects of catalase and peroxydase	0.005	0.994	0.000
E80.0 Hereditary erythropoietic porphyria	0.005	0.994	0.000
S01.9 Open wound of head, part unspecified	0.005	0.995	0.000
E80.6 Other disorders of bilirubin metabolism	0.005	0.995	0.000
H53.8 Other visual disturbances	0.000	0.995	0.005
G24.3 Spasmodic torticollis	0.005	0.995	0.000
N00-N08 Glomerular diseases	0.000	0.995	0.005
R41.0 Disorientation, unspecified	0.000	0.995	0.005
G24.1 Idiopathic familial dystonia	0.005	0.995	0.000
O16 Unspecified maternal hypertension	0.000	0.995	0.005
G24.4 Idiopathic orofacial dystonia	0.005	0.995	0.000
G24.2 Idiopathic nonfamilial dystonia	0.005	0.995	0.000
O36.5 Maternal care for poor foetal growth	0.000	0.995	0.005
O36.3 Maternal care for signs of foetal hypoxia	0.000	0.995	0.004
N76.2 Acute vulvitis	0.005	0.995	0.000
R44 Other symptoms and signs involving general sensations and perceptions	0.000	0.995	0.005
R40-R46 Symptoms and signs involving cognition, perception, emotional state and behaviour	0.000	0.995	0.005
H53.6 Night blindness	0.000	0.996	0.004
H53.5 Colour vision deficiencies	0.000	0.996	0.004
H53.3 Other disorders of binocular vision	0.000	0.996	0.004
R40 Somnolence, stupor and coma	0.000	0.996	0.004
N08.5 Glomerular disorders in systemic connective tissue disorders	0.000	0.996	0.004
G24.0 Drug-induced dystonia	0.004	0.996	0.000
N08 Glomerular disorders in diseases classified elsewhere	0.000	0.996	0.004
N04 Nephrotic syndrome	0.000	0.996	0.004
H53.2 Diplopia	0.000	0.996	0.004
O46.8 Other antepartum haemorrhage	0.000	0.996	0.004
R44.0 Auditory hallucinations	0.000	0.996	0.004
N45 Orchitis and epididymitis	0.004	0.996	0.000
N04.1 Focal and segmental glomerular lesions	0.000	0.996	0.004
M19.09 Primary arthrosis of other joints (Site unspecified)	0.004	0.996	0.000
N93.0 Postcoital and contact bleeding	0.000	0.996	0.004
G25 Other extrapyramidal and movement disorders	0.004	0.996	0.000
I89.0 Lymphoedema, not elsewhere classified	0.004	0.996	0.000
M77.47 Metatarsalgia-Ankle/Foot	0.004	0.996	0.000
R44.3 Hallucinations, unspecified	0.000	0.996	0.004
H06.2 Dysthyroid exophthalmos	0.004	0.996	0.000
R40.0 Somnolence	0.000	0.996	0.004
N07 Hereditary nephropathy, not elsewhere classified	0.000	0.996	0.004
N06 Isolated proteinuria with specified morphological lesion	0.000	0.996	0.004
N01 Rapidly progressive nephritic syndrome	0.000	0.996	0.004
E70-E90 Metabolic disorders	0.004	0.996	0.000
R40.1 Stupor	0.000	0.996	0.004
G20-G26 Extrapyramidal and movement disorders	0.004	0.996	0.000
R43 Disturbances of smell and taste	0.000	0.996	0.004
G25.3 Myoclonus	0.004	0.996	0.000
R44.1 Visual hallucinations	0.000	0.996	0.004
I46.0 Cardiac arrest with successful resuscitation	0.000	0.996	0.004
N00 Acute nephritic syndrome	0.000	0.996	0.003
G25.1 Drug-induced tremor	0.004	0.996	0.000
R43.8 Other and unspecified disturbances of smell and taste	0.000	0.996	0.004
E83.5 Disorders of calcium metabolism	0.003	0.996	0.000
G25.0 Essential tremor	0.004	0.996	0.000
R44.2 Other hallucinations	0.000	0.996	0.003
R40.2 Coma, unspecified	0.000	0.996	0.004
N03 Chronic nephritic syndrome	0.000	0.996	0.004
S52.00 Fracture of upper end of ulna (closed)	0.000	0.996	0.004
Q25.1 Coarctation of aorta	0.003	0.996	0.000
G21 Secondary Parkinsonism	0.003	0.996	0.000
I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified	0.003	0.997	0.000
I89 Other non-infective disorders of lymphatic vessels and lymph nodes	0.003	0.997	0.000
N08.8 Glomerular disorders in other diseases classified elsewhere	0.000	0.997	0.003
N08.2 Glomerular disorders in blood diseases and disorders involving the immune mechanism	0.000	0.997	0.003
N08.1 Glomerular disorders in neoplastic diseases	0.000	0.997	0.003
N08.0 Glomerular disorders in infectious and parasitic diseases classified elsewhere	0.000	0.997	0.003
N04.8 Other	0.000	0.997	0.003
N04.7 Diffuse crescentic glomerulonephritis	0.000	0.997	0.003
N04.6 Dense deposit disease	0.000	0.997	0.003
N04.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.997	0.003
N04.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.997	0.003
N04.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.997	0.003
K92 Other diseases of digestive system	0.000	0.997	0.003
R44.8 Other and unspecified symptoms and signs involving general sensations and perceptions	0.000	0.997	0.003
K92.8 Other specified diseases of digestive system	0.000	0.997	0.003
N04.9 Unspecified	0.000	0.997	0.003
R46.4 Slowness and poor responsiveness	0.000	0.997	0.003
G25.5 Other chorea	0.003	0.997	0.000
I89.9 Non-infective disorder of lymphatic vessels and lymph nodes, unspecified	0.003	0.997	0.000
N03.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.997	0.003
N08.4 Glomerular disorders in other endocrine, nutritional and metabolic diseases	0.000	0.997	0.003
N04.0 Minor glomerular abnormality	0.000	0.997	0.003
E74 Other disorders of carbohydrate metabolism	0.003	0.997	0.000
N45.0 Orchitis, epididymitis and epididymo-orchitis with abscess	0.003	0.997	0.000
E72 Other disorders of amino-acid metabolism	0.003	0.997	0.000
N04.2 Diffuse membranous glomerulonephritis	0.000	0.997	0.003
G25.6 Drug-induced tics and other tics of organic origin	0.003	0.997	0.000
G25.4 Drug-induced chorea	0.003	0.997	0.000
Q25 Congenital malformations of great arteries	0.003	0.997	0.000
G25.9 Extrapyramidal and movement disorder, unspecified	0.003	0.997	0.000
N03.1 Focal and segmental glomerular lesions	0.000	0.997	0.003
E75 Disorders of sphingolipid metabolism and other lipid storage disorders	0.003	0.997	0.000
R46 Symptoms and signs involving appearance and behaviour	0.000	0.997	0.003
G21.0 Malignant neuroleptic syndrome	0.003	0.997	0.000
C83.0 Small cell (diffuse)	0.000	0.997	0.003
R43.2 Parageusia	0.000	0.997	0.003
G23 Other degenerative diseases of basal ganglia	0.003	0.997	0.000
N01.9 Unspecified	0.000	0.997	0.003
N01.8 Other	0.000	0.997	0.003
N01.7 Diffuse crescentic glomerulonephritis	0.000	0.997	0.003
N01.6 Dense deposit disease	0.000	0.997	0.003
N01.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.997	0.003
N01.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.997	0.003
N01.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.997	0.003
N01.2 Diffuse membranous glomerulonephritis	0.000	0.997	0.003
N01.1 Focal and segmental glomerular lesions	0.000	0.997	0.003
N01.0 Minor glomerular abnormality	0.000	0.997	0.003
N03.8 Other	0.000	0.997	0.003
N06.9 Unspecified	0.000	0.997	0.003
N06.8 Other	0.000	0.997	0.003
N06.7 Diffuse crescentic glomerulonephritis	0.000	0.997	0.003
N06.6 Dense deposit disease	0.000	0.997	0.003
N06.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.997	0.003
N06.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.997	0.003
N06.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.997	0.003
N06.2 Diffuse membranous glomerulonephritis	0.000	0.997	0.003
N06.1 Focal and segmental glomerular lesions	0.000	0.997	0.003
N06.0 Minor glomerular abnormality	0.000	0.997	0.003
N07.9 Unspecified	0.000	0.997	0.003
N07.8 Other	0.000	0.997	0.003
N07.7 Diffuse crescentic glomerulonephritis	0.000	0.997	0.003
N07.6 Dense deposit disease	0.000	0.997	0.003
N07.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.997	0.003
N07.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.997	0.003
N07.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.997	0.003
N07.2 Diffuse membranous glomerulonephritis	0.000	0.997	0.003
N07.1 Focal and segmental glomerular lesions	0.000	0.997	0.003
N07.0 Minor glomerular abnormality	0.000	0.997	0.003
R43.1 Parosmia	0.000	0.997	0.003
E77 Disorders of glycoprotein metabolism	0.003	0.997	0.000
E76 Disorders of glycosaminoglycan metabolism	0.003	0.997	0.000
E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism	0.003	0.997	0.000
E90 Nutritional and metabolic disorders in diseases classified elsewhere	0.003	0.997	0.000
O46 Antepartum haemorrhage, not elsewhere classified	0.000	0.997	0.003
M75.2 Bicipital tendinitis	0.000	0.997	0.003
G26 Extrapyramidal and movement disorders in diseases classified elsewhere	0.003	0.997	0.000
G22 Parkinsonism in diseases classified elsewhere	0.003	0.997	0.000
G30.9 Alzheimer's disease, unspecified	0.003	0.997	0.000
G21.1 Other drug-induced secondary Parkinsonism	0.003	0.997	0.000
G25.8 Other specified extrapyramidal and movement disorders	0.003	0.997	0.000
I86.8 Varicose veins of other specified sites	0.003	0.997	0.000
N00.8 Other	0.000	0.997	0.003
N00.7 Diffuse crescentic glomerulonephritis	0.000	0.997	0.003
N00.6 Dense deposit disease	0.000	0.997	0.003
N00.5 Diffuse mesangiocapillary glomerulonephritis	0.000	0.997	0.003
N00.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.997	0.003
N00.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.997	0.003
N00.2 Diffuse membranous glomerulonephritis	0.000	0.997	0.003
N00.1 Focal and segmental glomerular lesions	0.000	0.997	0.003
N00.0 Minor glomerular abnormality	0.000	0.997	0.003
O46.9 Antepartum haemorrhage, unspecified	0.000	0.997	0.003
G21.4 Vascular parkinsonism	0.003	0.997	0.000
E70 Disorders of aromatic amino-acid metabolism	0.003	0.997	0.000
I86 Varicose veins of other sites	0.003	0.997	0.000
N03.7 Diffuse crescentic glomerulonephritis	0.000	0.997	0.003
N03.6 Dense deposit disease	0.000	0.997	0.003
N03.4 Diffuse endocapillary proliferative glomerulonephritis	0.000	0.997	0.003
N03.3 Diffuse mesangial proliferative glomerulonephritis	0.000	0.997	0.003
N03.2 Diffuse membranous glomerulonephritis	0.000	0.997	0.003
N03.0 Minor glomerular abnormality	0.000	0.997	0.003
Q25.6 Stenosis of pulmonary artery	0.003	0.997	0.000
E79 Disorders of purine and pyrimidine metabolism	0.003	0.997	0.000
G21.9 Secondary Parkinsonism, unspecified	0.003	0.997	0.000
G21.8 Other secondary Parkinsonism	0.003	0.997	0.000
G21.3 Postencephalitic Parkinsonism	0.003	0.997	0.000
G21.2 Secondary Parkinsonism due to other external agents	0.003	0.997	0.000
E74.3 Other disorders of intestinal carbohydrate absorption	0.003	0.997	0.000
A40.3 Septicaemia due to Streptococcus pneumoniae	0.000	0.997	0.003
E88 Other metabolic disorders	0.003	0.997	0.000
E73 Lactose intolerance	0.003	0.997	0.000
H90.5 Sensorineural hearing loss, unspecified	0.000	0.997	0.003
N08.3 Glomerular disorders in diabetes mellitus	0.000	0.997	0.003
Q27.8 Other specified congenital malformations of peripheral vascular system	0.003	0.997	0.000
E84 Cystic fibrosis	0.002	0.997	0.000
I46.9 Cardiac arrest, unspecified	0.000	0.997	0.003
I86.3 Vulval varices	0.003	0.997	0.000
N00.9 Unspecified	0.000	0.997	0.002
I82 Other venous embolism and thrombosis	0.003	0.997	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
G25.2 Other specified forms of tremor	0.002	0.997	0.000
E72.1 Disorders of sulphur-bearing amino-acid metabolism	0.002	0.997	0.000
E72.0 Disorders of amino-acid transport	0.002	0.997	0.000
D22.7 Melanocytic naevi of lower limb, including hip	0.000	0.997	0.003
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.997	0.000
Q25.4 Other congenital malformations of aorta	0.003	0.997	0.000
Q23 Congenital malformations of aortic and mitral valves	0.003	0.997	0.000
E74.9 Disorder of carbohydrate metabolism, unspecified	0.002	0.997	0.000
E74.8 Other specified disorders of carbohydrate metabolism	0.002	0.997	0.000
E74.4 Disorders of pyruvate metabolism and gluconeogenesis	0.002	0.997	0.000
E74.2 Disorders of galactose metabolism	0.002	0.997	0.000
E74.1 Disorders of fructose metabolism	0.002	0.997	0.000
E74.0 Glycogen storage disease	0.002	0.997	0.000
Q24 Other congenital malformations of heart	0.003	0.997	0.000
E72.9 Disorder of amino-acid metabolism, unspecified	0.002	0.997	0.000
E72.8 Other specified disorders of amino-acid metabolism	0.002	0.997	0.000
E72.5 Disorders of glycine metabolism	0.002	0.997	0.000
E72.4 Disorders of ornithine metabolism	0.002	0.997	0.000
E72.3 Disorders of lysine and hydroxylysine metabolism	0.002	0.997	0.000
E72.2 Disorders of urea cycle metabolism	0.002	0.997	0.000
E75.5 Other lipid storage disorders	0.002	0.997	0.000
E88.1 Lipodystrophy, not elsewhere classified	0.002	0.997	0.000
G23.1 Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]	0.002	0.997	0.000
N02 Recurrent and persistent haematuria	0.001	0.997	0.002
Q25.9 Congenital malformation of great arteries, unspecified	0.002	0.997	0.000
Q25.8 Other congenital malformations of great arteries	0.002	0.997	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.997	0.000
Q25.2 Atresia of aorta	0.002	0.997	0.000
K91 Postprocedural disorders of digestive system, not elsewhere classified	0.000	0.997	0.002
Q24.0 Dextrocardia	0.002	0.997	0.000
D22.0 Melanocytic naevi of lip	0.000	0.997	0.003
E75.6 Lipid storage disorder, unspecified	0.002	0.997	0.000
E75.4 Neuronal ceroid lipofuscinosis	0.002	0.997	0.000
E75.3 Sphingolipidosis, unspecified	0.002	0.997	0.000
E75.2 Other sphingolipidosis	0.002	0.997	0.000
E75.1 Other gangliosidosis	0.002	0.997	0.000
E75.0 GM2 gangliosidosis	0.002	0.997	0.000
Q24.5 Malformation of coronary vessels	0.002	0.997	0.000
R46.7 Verbosity and circumstantial detail obscuring reason for contact	0.000	0.997	0.002
R46.6 Undue concern and preoccupation with stressful events	0.000	0.997	0.002
R46.5 Suspiciousness and marked evasiveness	0.000	0.997	0.002
R46.3 Overactivity	0.000	0.997	0.002
R46.1 Bizarre personal appearance	0.000	0.997	0.002
Q23.1 Congenital insufficiency of aortic valve	0.002	0.997	0.000
G23.9 Degenerative disease of basal ganglia, unspecified	0.002	0.998	0.000
G23.3 Multiple system atrophy, cerebellar type	0.002	0.998	0.000
G23.2 Striatonigral degeneration	0.002	0.998	0.000
G23.0 Hallervorden-Spatz disease	0.002	0.998	0.000
I46 Cardiac arrest	0.000	0.998	0.002
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
E71.3 Disorders of fatty-acid metabolism	0.002	0.998	0.000
E71.2 Disorder of branched-chain amino-acid metabolism, unspecified	0.002	0.998	0.000
E71.1 Other disorders of branched-chain amino-acid metabolism	0.002	0.998	0.000
E71.0 Maple-syrup-urine disease	0.002	0.998	0.000
E76.9 Disorder of glucosaminoglycan metabolism, unspecified	0.002	0.998	0.000
E76.8 Other disorders of glucosaminoglycan metabolism	0.002	0.998	0.000
E76.3 Mucopolysaccharidosis, unspecified	0.002	0.998	0.000
E76.2 Other mucopolysaccharidoses	0.002	0.998	0.000
E76.1 Mucopolysaccharidosis, type II	0.002	0.998	0.000
E76.0 Mucopolysaccharidosis, type I	0.002	0.998	0.000
E77.9 Disorder of glycoprotein metabolism, unspecified	0.002	0.998	0.000
E77.8 Other disorders of glycoprotein metabolism	0.002	0.998	0.000
E77.1 Defects in glycoprotein degradation	0.002	0.998	0.000
E77.0 Defects in posttranslational modification of lysosomal enzymes	0.002	0.998	0.000
G23.8 Other specified degenerative diseases of basal ganglia	0.002	0.998	0.000
I82.3 Embolism and thrombosis of renal vein	0.002	0.998	0.000
O46.0 Antepartum haemorrhage with coagulation defect	0.000	0.998	0.002
Q25.0 Patent ductus arteriosus	0.002	0.998	0.000
E88.3 Tumour lysis syndrome	0.002	0.998	0.000
C67.2 Lateral wall of bladder	0.000	0.998	0.002
L03.2 Cellulitis of face	0.002	0.998	0.000
O42.9 Premature rupture of membranes, unspecified	0.000	0.998	0.002
M41.99 Scoliosis, unspecified (Site unspecified)	0.002	0.998	0.000
Q23.0 Congenital stenosis of aortic valve	0.002	0.998	0.000
M94.86 Other specified disorders of cartilage (Lower leg)	0.000	0.998	0.002
I82.2 Embolism and thrombosis of vena cava	0.002	0.998	0.000
I86.0 Sublingual varices	0.002	0.998	0.000
Q25.3 Stenosis of aorta	0.002	0.998	0.000
R46.0 Very low level of personal hygiene	0.000	0.998	0.002
Z76.8 Persons encountering health services in other specified circumstances	0.002	0.998	0.000
E70.9 Disorder of aromatic amino-acid metabolism, unspecified	0.002	0.998	0.000
E70.8 Other disorders of aromatic amino-acid metabolism	0.002	0.998	0.000
E70.2 Disorders of tyrosine metabolism	0.002	0.998	0.000
E70.1 Other hyperphenylalaninaemias	0.002	0.998	0.000
E70.0 Classical phenylketonuria	0.002	0.998	0.000
K21.0 Gastro-oesophageal reflux disease with oesophagitis	0.002	0.998	0.000
I88 Nonspecific lymphadenitis	0.002	0.998	0.000
N40 Hyperplasia of prostate	0.002	0.998	0.000
N36.9 Urethral disorder, unspecified	0.002	0.998	0.000
O69.2 Labour and delivery complicated by other cord entanglement	0.002	0.998	0.000
E88.8 Other specified metabolic disorders	0.002	0.998	0.000
I89.1 Lymphangitis	0.002	0.998	0.000
E79.9 Disorder of purine and pyrimidine metabolism, unspecified	0.002	0.998	0.000
E79.8 Other disorders of purine and pyrimidine metabolism	0.002	0.998	0.000
E79.1 Lesch-Nyhan syndrome	0.002	0.998	0.000
Q24.4 Congenital subaortic stenosis	0.002	0.998	0.000
T90.9 Sequelae of unspecified injury of head	0.002	0.998	0.000
E73.8 Other lactose intolerance	0.002	0.998	0.000
E73.1 Secondary lactase deficiency	0.002	0.998	0.000
E73.0 Congenital lactase deficiency	0.002	0.998	0.000
R43.0 Anosmia	0.000	0.998	0.002
E88.9 Metabolic disorder, unspecified	0.002	0.998	0.000
N02.0 Minor glomerular abnormality	0.000	0.998	0.002
N02.2 Diffuse membranous glomerulonephritis	0.000	0.998	0.002
M94.88 Other specified disorders of cartilage (Other)	0.000	0.998	0.002
E84.8 Cystic fibrosis with other manifestations	0.002	0.998	0.000
E84.1 Cystic fibrosis with intestinal manifestations	0.002	0.998	0.000
E84.0 Cystic fibrosis with pulmonary manifestations	0.002	0.998	0.000
I82.1 Thrombophlebitis migrans	0.002	0.998	0.000
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
K91.9 Postprocedural disorder of digestive system, unspecified	0.000	0.998	0.002
Q24.6 Congenital heart block	0.002	0.998	0.000
R20.2 Paraesthesia of skin	0.000	0.998	0.002
G30 Alzheimer's disease	0.002	0.998	0.000
E70.3 Albinism	0.002	0.998	0.000
Q28.3 Other malformations of cerebral vessels	0.002	0.998	0.000
W49.0 Home	0.000	0.998	0.002
E85 Amyloidosis	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.002	0.998	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q23.4 Hypoplastic left heart syndrome	0.002	0.998	0.000
Q23.2 Congenital mitral stenosis	0.002	0.998	0.000
O43.1 Malformation of placenta	0.000	0.998	0.002
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
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
I82.0 Budd-Chiari syndrome	0.002	0.998	0.000
N02.7 Diffuse crescentic glomerulonephritis	0.001	0.998	0.002
N02.6 Dense deposit disease	0.001	0.998	0.002
N02.5 Diffuse mesangiocapillary glomerulonephritis	0.001	0.998	0.002
N02.4 Diffuse endocapillary proliferative glomerulonephritis	0.001	0.998	0.002
N02.1 Focal and segmental glomerular lesions	0.001	0.998	0.002
I60 Subarachnoid haemorrhage	0.000	0.998	0.002
M10.96 Gout, unspecified (Lower leg)	0.000	0.998	0.002
Q22 Congenital malformations of pulmonary and tricuspid valves	0.002	0.998	0.000
M13.00 Polyarthritis, unspecified (Multiple sites)	0.000	0.998	0.002
D22.9 Melanocytic naevi, unspecified	0.000	0.998	0.002
H27.1 Dislocation of lens	0.000	0.998	0.002
I08.3 Combined disorders of mitral, aortic and tricuspid valves	0.002	0.998	0.000
N50.9 Disorder of male genital organs, unspecified	0.002	0.998	0.000
I86.2 Pelvic varices	0.002	0.998	0.000
M77.4 Metatarsalgia	0.002	0.998	0.000
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
D69 Purpura and other haemorrhagic conditions	0.002	0.998	0.000
E79.0 Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease	0.002	0.998	0.000
E88.2 Lipomatosis, not elsewhere classified	0.002	0.998	0.000
I60.2 Subarachnoid haemorrhage from anterior communicating artery	0.000	0.998	0.002
N02.3 Diffuse mesangial proliferative glomerulonephritis	0.001	0.998	0.002
Q21.0 Ventricular septal defect	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
C85.9 Non-Hodgkin's lymphoma, unspecified type	0.000	0.998	0.002
G30.0 Alzheimer's disease with early onset	0.002	0.998	0.000
K91.1 Postgastric surgery syndromes	0.000	0.998	0.002
D22 Melanocytic naevi	0.000	0.998	0.002
I46.1 Sudden cardiac death, so described	0.000	0.998	0.002
K91.5 Postcholecystectomy syndrome	0.000	0.998	0.002
Q23.3 Congenital mitral insufficiency	0.002	0.998	0.000
G30.1 Alzheimer's disease with late onset	0.002	0.998	0.000
I82.8 Embolism and thrombosis of other specified veins	0.002	0.998	0.000
D69.2 Other nonthrombocytopenic purpura	0.002	0.998	0.000
H27.0 Aphakia	0.000	0.998	0.002
I88.9 Nonspecific lymphadenitis, unspecified	0.002	0.998	0.000
O43.8 Other placental disorders	0.000	0.998	0.002
H53.0 Amblyopia ex anopsia	0.000	0.998	0.002
I86.1 Scrotal varices	0.002	0.998	0.000
I88.1 Chronic lymphadenitis, except mesenteric	0.002	0.998	0.000
O35.9 Maternal care for (suspected) foetal abnormality and damage, unspecified	0.000	0.998	0.002
R30.0 Dysuria	0.002	0.998	0.000
E85.8 Other amyloidosis	0.002	0.998	0.000
M94.8 Other specified disorders of cartilage	0.000	0.998	0.002
N02.9 Unspecified	0.002	0.998	0.000
R46.2 Strange and inexplicable behaviour	0.000	0.998	0.002
C48.2 Peritoneum, unspecified	0.002	0.998	0.000
E73.9 Lactose intolerance, unspecified	0.002	0.998	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.002	0.998	0.000
G30.8 Other Alzheimer's disease	0.002	0.998	0.000
D69.8 Other specified haemorrhagic conditions	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