TreeWAS – Variant ID: rs2361502

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
E80.4 Gilbert's syndrome	1.000	0.000	0.000
E80 Disorders of porphyrin and bilirubin metabolism	0.749	0.251	0.000
E80.6 Other disorders of bilirubin metabolism	0.699	0.301	0.000
E80.2 Other porphyria	0.539	0.461	0.000
E80.7 Disorder of bilirubin metabolism, unspecified	0.537	0.463	0.000
E80.5 Crigler-Najjar syndrome	0.537	0.463	0.000
E80.3 Defects of catalase and peroxydase	0.537	0.463	0.000
E80.0 Hereditary erythropoietic porphyria	0.537	0.463	0.000
E80.1 Porphyria cutanea tarda	0.527	0.473	0.000
I08 Multiple valve diseases	0.000	0.947	0.053
I05 Rheumatic mitral valve diseases	0.000	0.948	0.052
I05-I09 Chronic rheumatic heart diseases	0.000	0.948	0.052
I08.1 Disorders of both mitral and tricuspid valves	0.000	0.950	0.050
I05.2 Mitral stenosis with insufficiency	0.000	0.952	0.048
I07 Rheumatic tricuspid valve diseases	0.000	0.952	0.048
I05.0 Mitral stenosis	0.000	0.953	0.047
I08.0 Disorders of both mitral and aortic valves	0.000	0.953	0.047
I07.1 Tricuspid insufficiency	0.000	0.955	0.045
I08.9 Multiple valve disease, unspecified	0.000	0.956	0.044
I08.3 Combined disorders of mitral, aortic and tricuspid valves	0.000	0.956	0.044
I05.9 Mitral valve disease, unspecified	0.000	0.957	0.043
I09 Other rheumatic heart diseases	0.000	0.960	0.040
I08.2 Disorders of both aortic and tricuspid valves	0.000	0.962	0.038
I05.8 Other mitral valve diseases	0.000	0.962	0.038
I05.1 Rheumatic mitral insufficiency	0.000	0.963	0.037
I07.9 Tricuspid valve disease, unspecified	0.000	0.966	0.034
I07.8 Other tricuspid valve diseases	0.000	0.966	0.034
I07.2 Tricuspid stenosis with insufficiency	0.000	0.966	0.034
I07.0 Tricuspid stenosis	0.000	0.966	0.034
I06 Rheumatic aortic valve diseases	0.000	0.968	0.032
I09.9 Rheumatic heart disease, unspecified	0.000	0.968	0.032
I08.8 Other multiple valve diseases	0.000	0.970	0.030
I09.8 Other specified rheumatic heart diseases	0.000	0.971	0.029
I09.2 Chronic rheumatic pericarditis	0.000	0.971	0.029
I09.1 Rheumatic diseases of endocardium, valve unspecified	0.000	0.971	0.029
I09.0 Rheumatic myocarditis	0.000	0.971	0.029
I06.9 Rheumatic aortic valve disease, unspecified	0.000	0.977	0.023
I06.8 Other rheumatic aortic valve diseases	0.000	0.977	0.023
I06.2 Rheumatic aortic stenosis with insufficiency	0.000	0.977	0.023
I06.1 Rheumatic aortic insufficiency	0.000	0.978	0.022
I06.0 Rheumatic aortic stenosis	0.000	0.980	0.020
L57.0 Actinic keratosis	0.000	0.982	0.018
F31 Bipolar affective disorder	0.016	0.984	0.000
L42 Pityriasis rosea	0.016	0.984	0.000
F31.0 Bipolar affective disorder, current episode hypomanic	0.015	0.985	0.000
F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms	0.014	0.986	0.000
F31.1 Bipolar affective disorder, current episode manic without psychotic symptoms	0.014	0.986	0.000
F31.3 Bipolar affective disorder, current episode mild or moderate depression	0.014	0.986	0.000
F31.6 Bipolar affective disorder, current episode mixed	0.014	0.986	0.000
R94.3 Abnormal results of cardiovascular function studies	0.000	0.987	0.013
F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms	0.013	0.987	0.000
N41.9 Inflammatory disease of prostate, unspecified	0.000	0.988	0.012
R17 Unspecified jaundice	0.012	0.988	0.000
F31.8 Other bipolar affective disorders	0.011	0.988	0.000
F31.4 Bipolar affective disorder, current episode severe depression without psychotic symptoms	0.011	0.989	0.000
E10.9 Without complications	0.011	0.989	0.000
N41.0 Acute prostatitis	0.000	0.990	0.010
F31.7 Bipolar affective disorder, currently in remission	0.010	0.990	0.000
N41 Inflammatory diseases of prostate	0.000	0.990	0.010
F30-F39 Mood [affective] disorders	0.009	0.991	0.000
F39 Unspecified mood [affective] disorder	0.009	0.991	0.000
F31.9 Bipolar affective disorder, unspecified	0.009	0.991	0.000
Z02.8 Other examinations for administrative purposes	0.000	0.992	0.008
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency	0.000	0.992	0.008
E70-E90 Metabolic disorders	0.008	0.992	0.000
K10.8 Other specified diseases of jaws	0.000	0.992	0.008
N41.8 Other inflammatory diseases of prostate	0.000	0.992	0.008
N41.3 Prostatocystitis	0.000	0.993	0.007
N41.2 Abscess of prostate	0.000	0.993	0.007
F34 Persistent mood [affective] disorders	0.007	0.993	0.000
F32 Depressive episode	0.007	0.993	0.000
F38 Other mood [affective] disorders	0.007	0.993	0.000
F30 Manic episode	0.007	0.993	0.000
E16.2 Hypoglycaemia, unspecified	0.007	0.993	0.000
E79 Disorders of purine and pyrimidine metabolism	0.006	0.993	0.000
E70 Disorders of aromatic amino-acid metabolism	0.006	0.993	0.000
F32.8 Other depressive episodes	0.006	0.993	0.000
E84 Cystic fibrosis	0.006	0.993	0.000
F32.0 Mild depressive episode	0.006	0.994	0.000
D51 Vitamin B12 deficiency anaemia	0.000	0.994	0.006
D51.9 Vitamin B12 deficiency anaemia, unspecified	0.000	0.994	0.006
E88 Other metabolic disorders	0.006	0.994	0.000
F30.2 Mania with psychotic symptoms	0.006	0.994	0.000
E72 Other disorders of amino-acid metabolism	0.006	0.994	0.000
E77 Disorders of glycoprotein metabolism	0.006	0.994	0.000
E76 Disorders of glycosaminoglycan metabolism	0.006	0.994	0.000
E75 Disorders of sphingolipid metabolism and other lipid storage disorders	0.006	0.994	0.000
E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism	0.006	0.994	0.000
E90 Nutritional and metabolic disorders in diseases classified elsewhere	0.006	0.994	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.000	0.994	0.006
E74 Other disorders of carbohydrate metabolism	0.006	0.994	0.000
K10 Other diseases of jaws	0.000	0.994	0.006
K76.0 Fatty (change of) liver, not elsewhere classified	0.006	0.994	0.000
N41.1 Chronic prostatitis	0.000	0.994	0.006
E89 Postprocedural endocrine and metabolic disorders, not elsewhere classified	0.006	0.994	0.000
F34.1 Dysthymia	0.006	0.994	0.000
F32.1 Moderate depressive episode	0.006	0.994	0.000
F34.9 Persistent mood [affective] disorder, unspecified	0.005	0.995	0.000
F34.8 Other persistent mood [affective] disorders	0.005	0.995	0.000
F34.0 Cyclothymia	0.005	0.995	0.000
E79.0 Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease	0.005	0.995	0.000
E70.3 Albinism	0.005	0.995	0.000
E84.9 Cystic fibrosis, unspecified	0.005	0.995	0.000
K57.2 Diverticular disease of large intestine with perforation and abscess	0.000	0.995	0.005
T40.4 Other synthetic narcotics	0.005	0.995	0.000
E88.3 Tumour lysis syndrome	0.005	0.995	0.000
F38.8 Other specified mood [affective] disorders	0.005	0.995	0.000
F38.1 Other recurrent mood [affective] disorders	0.005	0.995	0.000
F38.0 Other single mood [affective] disorders	0.005	0.995	0.000
F32.2 Severe depressive episode without psychotic symptoms	0.005	0.995	0.000
F30.8 Other manic episodes	0.005	0.995	0.000
F30.1 Mania without psychotic symptoms	0.005	0.995	0.000
F32.3 Severe depressive episode with psychotic symptoms	0.005	0.995	0.000
E88.2 Lipomatosis, not elsewhere classified	0.005	0.995	0.000
E89.0 Postprocedural hypothyroidism	0.005	0.995	0.000
O36.0 Maternal care for rhesus isoimmunisation	0.005	0.995	0.000
E73 Lactose intolerance	0.005	0.995	0.000
E88.8 Other specified metabolic disorders	0.005	0.995	0.000
F33.0 Recurrent depressive disorder, current episode mild	0.005	0.995	0.000
K10.0 Developmental disorders of jaws	0.000	0.995	0.005
E70.9 Disorder of aromatic amino-acid metabolism, unspecified	0.005	0.995	0.000
E70.8 Other disorders of aromatic amino-acid metabolism	0.005	0.995	0.000
E70.2 Disorders of tyrosine metabolism	0.005	0.995	0.000
E70.1 Other hyperphenylalaninaemias	0.005	0.995	0.000
E70.0 Classical phenylketonuria	0.005	0.995	0.000
E78.4 Other hyperlipidaemia	0.005	0.995	0.000
E79.9 Disorder of purine and pyrimidine metabolism, unspecified	0.005	0.995	0.000
E79.8 Other disorders of purine and pyrimidine metabolism	0.005	0.995	0.000
E79.1 Lesch-Nyhan syndrome	0.005	0.995	0.000
E84.8 Cystic fibrosis with other manifestations	0.005	0.995	0.000
E84.1 Cystic fibrosis with intestinal manifestations	0.005	0.995	0.000
E84.0 Cystic fibrosis with pulmonary manifestations	0.005	0.995	0.000
K10.3 Alveolitis of jaws	0.000	0.995	0.005
F30.9 Manic episode, unspecified	0.005	0.995	0.000
S82.50 Fracture of medial malleolus (closed)	0.000	0.995	0.005
K10.2 Inflammatory conditions of jaws	0.000	0.995	0.005
F33 Recurrent depressive disorder	0.005	0.995	0.000
L57 Skin changes due to chronic exposure to nonionising radiation	0.000	0.995	0.005
E85 Amyloidosis	0.005	0.995	0.000
D51.8 Other vitamin B12 deficiency anaemias	0.000	0.995	0.005
D51.3 Other dietary vitamin B12 deficiency anaemia	0.000	0.995	0.005
D51.2 Transcobalamin II deficiency	0.000	0.995	0.005
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria	0.000	0.995	0.005
E72.0 Disorders of amino-acid transport	0.005	0.995	0.000
E88.9 Metabolic disorder, unspecified	0.005	0.995	0.000
E16 Other disorders of pancreatic internal secretion	0.005	0.995	0.000
K10.9 Disease of jaws, unspecified	0.000	0.995	0.005
E72.9 Disorder of amino-acid metabolism, unspecified	0.005	0.995	0.000
E72.8 Other specified disorders of amino-acid metabolism	0.005	0.995	0.000
E72.5 Disorders of glycine metabolism	0.005	0.995	0.000
E72.4 Disorders of ornithine metabolism	0.005	0.995	0.000
E72.3 Disorders of lysine and hydroxylysine metabolism	0.005	0.995	0.000
E72.2 Disorders of urea cycle metabolism	0.005	0.995	0.000
E72.1 Disorders of sulphur-bearing amino-acid metabolism	0.005	0.995	0.000
E71.3 Disorders of fatty-acid metabolism	0.004	0.995	0.000
E71.2 Disorder of branched-chain amino-acid metabolism, unspecified	0.004	0.995	0.000
E71.1 Other disorders of branched-chain amino-acid metabolism	0.004	0.995	0.000
E71.0 Maple-syrup-urine disease	0.004	0.995	0.000
E75.6 Lipid storage disorder, unspecified	0.004	0.995	0.000
E75.5 Other lipid storage disorders	0.004	0.995	0.000
E75.4 Neuronal ceroid lipofuscinosis	0.004	0.995	0.000
E75.3 Sphingolipidosis, unspecified	0.004	0.995	0.000
E75.2 Other sphingolipidosis	0.004	0.995	0.000
E75.1 Other gangliosidosis	0.004	0.995	0.000
E75.0 GM2 gangliosidosis	0.004	0.995	0.000
E76.9 Disorder of glucosaminoglycan metabolism, unspecified	0.004	0.995	0.000
E76.8 Other disorders of glucosaminoglycan metabolism	0.004	0.995	0.000
E76.3 Mucopolysaccharidosis, unspecified	0.004	0.995	0.000
E76.2 Other mucopolysaccharidoses	0.004	0.995	0.000
E76.1 Mucopolysaccharidosis, type II	0.004	0.995	0.000
E76.0 Mucopolysaccharidosis, type I	0.004	0.995	0.000
E77.9 Disorder of glycoprotein metabolism, unspecified	0.004	0.995	0.000
E77.8 Other disorders of glycoprotein metabolism	0.004	0.995	0.000
E77.1 Defects in glycoprotein degradation	0.004	0.995	0.000
E77.0 Defects in posttranslational modification of lysosomal enzymes	0.004	0.995	0.000
T40.2 Other opioids	0.005	0.995	0.000
E74.9 Disorder of carbohydrate metabolism, unspecified	0.004	0.995	0.000
E74.8 Other specified disorders of carbohydrate metabolism	0.004	0.995	0.000
E74.4 Disorders of pyruvate metabolism and gluconeogenesis	0.004	0.995	0.000
E74.2 Disorders of galactose metabolism	0.004	0.995	0.000
E74.1 Disorders of fructose metabolism	0.004	0.995	0.000
E74.0 Glycogen storage disease	0.004	0.995	0.000
E89.8 Other postprocedural endocrine and metabolic disorders	0.004	0.995	0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.000	0.996	0.004
K10.1 Giant cell granuloma, central	0.000	0.996	0.004
E89.9 Postprocedural endocrine and metabolic disorder, unspecified	0.004	0.996	0.000
E89.5 Postprocedural testicular hypofunction	0.004	0.996	0.000
E89.4 Postprocedural ovarian failure	0.004	0.996	0.000
E89.1 Postprocedural hypoinsulinaemia	0.004	0.996	0.000
E88.1 Lipodystrophy, not elsewhere classified	0.004	0.996	0.000
B44.1 Other pulmonary aspergillosis	0.004	0.996	0.000
E74.3 Other disorders of intestinal carbohydrate absorption	0.004	0.996	0.000
I27.0 Primary pulmonary hypertension	0.000	0.996	0.004
E16.1 Other hypoglycaemia	0.004	0.996	0.000
E89.6 Postprocedural adrenocortical(-medullary) hypofunction	0.004	0.996	0.000
T40 Poisoning by narcotics and psychodysleptics [hallucinogens]	0.004	0.996	0.000
F30.0 Hypomania	0.004	0.996	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.000	0.996	0.004
E89.3 Postprocedural hypopituitarism	0.004	0.996	0.000
E73.8 Other lactose intolerance	0.004	0.996	0.000
E73.1 Secondary lactase deficiency	0.004	0.996	0.000
E73.0 Congenital lactase deficiency	0.004	0.996	0.000
F33.3 Recurrent depressive disorder, current episode severe with psychotic symptoms	0.004	0.996	0.000
Q38.7 Pharyngeal pouch	0.004	0.996	0.000
E85.8 Other amyloidosis	0.004	0.996	0.000
E85.2 Heredofamilial amyloidosis, unspecified	0.004	0.996	0.000
E85.1 Neuropathic heredofamilial amyloidosis	0.004	0.996	0.000
E85.0 Nonneuropathic heredofamilial amyloidosis	0.004	0.996	0.000
F33.8 Other recurrent depressive disorders	0.004	0.996	0.000
F33.4 Recurrent depressive disorder, currently in remission	0.004	0.996	0.000
L57.5 Actinic granuloma	0.000	0.996	0.004
L57.3 Poikiloderma of Civatte	0.000	0.996	0.004
L57.2 Cutis rhomboidalis nuchae	0.000	0.996	0.004
L57.1 Actinic reticuloid	0.000	0.996	0.004
E78.8 Other disorders of lipoprotein metabolism	0.004	0.996	0.000
E85.3 Secondary systemic amyloidosis	0.004	0.996	0.000
D89.1 Cryoglobulinaemia	0.000	0.996	0.004
E16.9 Disorder of pancreatic internal secretion, unspecified	0.004	0.996	0.000
E16.8 Other specified disorders of pancreatic internal secretion	0.004	0.996	0.000
E16.4 Abnormal secretion of gastrin	0.004	0.996	0.000
E16.3 Increased secretion of glucagon	0.004	0.996	0.000
E78 Disorders of lipoprotein metabolism and other lipidaemias	0.004	0.996	0.000
E88.0 Disorders of plasma-protein metabolism, not elsewhere classified	0.004	0.996	0.000
L57.4 Cutis laxa senilis	0.000	0.996	0.003
E85.9 Amyloidosis, unspecified	0.003	0.996	0.000
Z02 Examination and encounter for administrative purposes	0.000	0.996	0.004
D89.0 Polyclonal hypergammaglobulinaemia	0.000	0.996	0.003
D89.3 Immune reconstitution syndrome	0.000	0.997	0.003
L57.9 Skin changes due to chronic exposure to nonionising radiation, unspecified	0.000	0.997	0.003
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.000	0.997	0.003
T40.5 Cocaine	0.003	0.997	0.000
E16.0 Drug-induced hypoglycaemia without coma	0.003	0.997	0.000
L60.8 Other nail disorders	0.003	0.997	0.000
T40.9 Other and unspecified psychodysleptics [hallucinogens]	0.003	0.997	0.000
T40.8 Lysergide [LSD]	0.003	0.997	0.000
T40.7 Cannabis (derivatives)	0.003	0.997	0.000
T40.3 Methadone	0.003	0.997	0.000
T40.1 Heroin	0.003	0.997	0.000
T40.0 Opium	0.003	0.997	0.000
T40.6 Other and unspecified narcotics	0.003	0.997	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.003	0.997	0.000
F33.1 Recurrent depressive disorder, current episode moderate	0.003	0.997	0.000
K80.2 Calculus of gallbladder without cholecystitis	0.003	0.997	0.000
E15-E16 Other disorders of glucose regulation and pancreatic internal secretion	0.003	0.997	0.000
E78.3 Hyperchylomicronaemia	0.003	0.997	0.000
E89.2 Postprocedural hypoparathyroidism	0.003	0.997	0.000
Z02.9 Examination for administrative purposes, unspecified	0.000	0.997	0.003
Z02.7 Issue of medical certificate	0.000	0.997	0.003
Z02.6 Examination for insurance purposes	0.000	0.997	0.003
Z02.5 Examination for participation in sport	0.000	0.997	0.003
Z02.4 Examination for driving licence	0.000	0.997	0.003
Z02.3 Examination for recruitment to armed forces	0.000	0.997	0.003
Z02.2 Examination for admission to residential institution	0.000	0.997	0.003
Z02.1 Pre-employment examination	0.000	0.997	0.003
Z02.0 Examination for admission to educational institution	0.000	0.997	0.003
E10 Insulin-dependent diabetes mellitus	0.003	0.997	0.000
B44 Aspergillosis	0.003	0.997	0.000
Q38.8 Other congenital malformations of pharynx	0.003	0.997	0.000
Q38.6 Other congenital malformations of mouth	0.003	0.997	0.000
E85.4 Organ-limited amyloidosis	0.002	0.997	0.000
E73.9 Lactose intolerance, unspecified	0.002	0.997	0.000
E78.6 Lipoprotein deficiency	0.003	0.997	0.000
B44.9 Aspergillosis, unspecified	0.003	0.997	0.000
Z97.4 Presence of external hearing-aid	0.003	0.997	0.000
E78.9 Disorder of lipoprotein metabolism, unspecified	0.003	0.997	0.000
N08.3 Glomerular disorders in diabetes mellitus	0.003	0.997	0.000
E10.2 With renal complications	0.002	0.997	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.997	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.002	0.997	0.000
Q38.3 Other congenital malformations of tongue	0.002	0.997	0.000
Q38.2 Macroglossia	0.002	0.997	0.000
Q38.1 Ankyloglossia	0.002	0.997	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.997	0.000
G31.8 Other specified degenerative diseases of nervous system	0.000	0.998	0.002
E15 Nondiabetic hypoglycaemic coma	0.002	0.998	0.000
L40-L45 Papulosquamous disorders	0.002	0.998	0.000
D80 Immunodeficiency with predominantly antibody defects	0.000	0.998	0.002
E10.8 With unspecified complications	0.002	0.998	0.000
E10.5 With peripheral circulatory complications	0.002	0.998	0.000
S06.00 Concussion (without open intracranial wound)	0.002	0.998	0.000
E10.7 With multiple complications	0.002	0.998	0.000
D80-D89 Certain disorders involving the immune mechanism	0.000	0.998	0.002
B44.8 Other forms of aspergillosis	0.002	0.998	0.000
B44.7 Disseminated aspergillosis	0.002	0.998	0.000
B44.2 Tonsillar aspergillosis	0.002	0.998	0.000
B44.0 Invasive pulmonary aspergillosis	0.002	0.998	0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.000	0.998	0.002
F80.1 Expressive language disorder	0.002	0.998	0.000
G70.0 Myasthenia gravis	0.000	0.998	0.002
D80.1 Nonfamilial hypogammaglobulinaemia	0.000	0.998	0.002
G93.1 Anoxic brain damage, not elsewhere classified	0.002	0.998	0.000
I27 Other pulmonary heart diseases	0.000	0.998	0.002
E10.4 With neurological complications	0.002	0.998	0.000
I27.8 Other specified pulmonary heart diseases	0.000	0.998	0.002
Z94.0 Kidney transplant status	0.002	0.998	0.000
E78.2 Mixed hyperlipidaemia	0.002	0.998	0.000
L55-L59 Radiation-related disorders of the skin and subcutaneous tissue	0.000	0.998	0.002
E10.6 With other specified complications	0.002	0.998	0.000
N36.2 Urethral caruncle	0.002	0.998	0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.000	0.998	0.002
F33.2 Recurrent depressive disorder, current episode severe without psychotic symptoms	0.002	0.998	0.000
S27.00 Traumatic pneumothorax (without open wound into thoracic cavity)	0.000	0.998	0.002
D82 Immunodeficiency associated with other major defects	0.000	0.998	0.002
L44 Other papulosquamous disorders	0.002	0.998	0.000
L41 Parapsoriasis	0.002	0.998	0.000
L45 Papulosquamous disorders in diseases classified elsewhere	0.002	0.998	0.000
D80.8 Other immunodeficiencies with predominantly antibody defects	0.000	0.998	0.002
D80.7 Transient hypogammaglobulinaemia of infancy	0.000	0.998	0.002
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.000	0.998	0.002
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.000	0.998	0.002
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.000	0.998	0.002
D80.0 Hereditary hypogammaglobulinaemia	0.000	0.998	0.002
E10.3 With ophthalmic complications	0.002	0.998	0.000
E11.2 With renal complications	0.002	0.998	0.000
E78.1 Pure hyperglyceridaemia	0.002	0.998	0.000
D50-D53 Nutritional anaemias	0.000	0.998	0.002
H43.3 Other vitreous opacities	0.002	0.998	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.000	0.998	0.002
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
D81 Combined immunodeficiencies	0.000	0.998	0.002
L56 Other acute skin changes due to ultraviolet radiation	0.000	0.998	0.002
G31.0 Circumscribed brain atrophy	0.000	0.998	0.002
N36.3 Prolapsed urethral mucosa	0.002	0.998	0.000
I27.1 Kyphoscoliotic heart disease	0.000	0.998	0.002
L56.8 Other specified acute skin changes due to ultraviolet radiation	0.000	0.998	0.002
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
L57.8 Other skin changes due to chronic exposure to nonionising radiation	0.000	0.998	0.002
D82.1 Di George's syndrome	0.000	0.998	0.002
E10.0 With coma	0.002	0.998	0.000
D83 Common variable immunodeficiency	0.000	0.998	0.002
S82.5 Fracture of medial malleolus	0.000	0.998	0.002
L55 Sunburn	0.000	0.998	0.002
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
H25.0 Senile incipient cataract	0.000	0.998	0.002
K26.3 Acute without haemorrhage or perforation	0.000	0.998	0.002
K80.5 Calculus of bile duct without cholangitis or cholecystitis	0.002	0.998	0.000
Q62.5 Duplication of ureter	0.002	0.998	0.000
D52 Folate deficiency anaemia	0.000	0.998	0.002
D53 Other nutritional anaemias	0.000	0.998	0.002
D82.9 Immunodeficiency associated with major defect, unspecified	0.000	0.998	0.001
D82.8 Immunodeficiency associated with other specified major defects	0.000	0.998	0.001
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.000	0.998	0.001
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.000	0.998	0.001
D82.2 Immunodeficiency with short-limbed stature	0.000	0.998	0.001
D82.0 Wiskott-Aldrich syndrome	0.000	0.998	0.001
L41.9 Parapsoriasis, unspecified	0.001	0.998	0.000
L41.8 Other parapsoriasis	0.001	0.998	0.000
L41.5 Retiform parapsoriasis	0.001	0.998	0.000
L41.4 Large plaque parapsoriasis	0.001	0.998	0.000
L41.3 Small plaque parapsoriasis	0.001	0.998	0.000
L41.2 Lymphomatoid papulosis	0.001	0.998	0.000
L41.1 Pityriasis lichenoides chronica	0.001	0.998	0.000
L41.0 Pityriasis lichenoides et varioliformis acuta	0.001	0.998	0.000
L44.9 Papulosquamous disorder, unspecified	0.001	0.998	0.000
L44.8 Other specified papulosquamous disorders	0.001	0.998	0.000
L44.4 Infantile papular acrodermatitis [Giannotti-Crosti]	0.001	0.998	0.000
L44.3 Lichen ruber moniliformis	0.001	0.998	0.000
L44.2 Lichen striatus	0.001	0.998	0.000
L44.1 Lichen nitidus	0.001	0.998	0.000
L44.0 Pityriasis rubra pilaris	0.001	0.998	0.000
G31 Other degenerative diseases of nervous system, not elsewhere classified	0.000	0.998	0.002
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
D84 Other immunodeficiencies	0.000	0.998	0.002
Q45.8 Other specified congenital malformations of digestive system	0.002	0.998	0.000
W06.0 Home	0.002	0.998	0.000
Z83.3 Family history of diabetes mellitus	0.000	0.998	0.002
L59 Other disorders of skin and subcutaneous tissue related to radiation	0.000	0.998	0.001
L58 Radiodermatitis	0.000	0.998	0.001
D81.9 Combined immunodeficiency, unspecified	0.000	0.998	0.001
D81.8 Other combined immunodeficiencies	0.000	0.998	0.001
D81.7 Major histocompatibility complex class II deficiency	0.000	0.998	0.001
D81.6 Major histocompatibility complex class I deficiency	0.000	0.998	0.001
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.000	0.998	0.001
D81.4 Nezelof's syndrome	0.000	0.998	0.001
D81.3 Adenosine deaminase [ADA] deficiency	0.000	0.998	0.001
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.000	0.998	0.001
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.000	0.998	0.001
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.000	0.998	0.001
D86.8 Sarcoidosis of other and combined sites	0.000	0.998	0.002
E86 Volume depletion	0.002	0.998	0.000
L56.4 Polymorphous light eruption	0.000	0.998	0.001
L56.3 Solar urticaria	0.000	0.998	0.001
L56.2 Photocontact dermatitis [berloque dermatitis]	0.000	0.998	0.001
L56.1 Drug photoallergic response	0.000	0.998	0.001
L56.0 Drug phototoxic response	0.000	0.998	0.001
N36.0 Urethral fistula	0.002	0.998	0.000
F80 Specific developmental disorders of speech and language	0.002	0.998	0.000
D47.2 Monoclonal gammopathy	0.000	0.998	0.002
G31.2 Degeneration of nervous system due to alcohol	0.000	0.998	0.002
H74.8 Other specified disorders of middle ear and mastoid	0.002	0.998	0.000
L56.9 Acute skin change due to ultraviolet radiation, unspecified	0.000	0.998	0.001
S00.7 Multiple superficial injuries of head	0.000	0.998	0.002
Y41.8 Other specified systemic anti-infectives and antiparasitics	0.002	0.998	0.000
F52.2 Failure of genital response	0.002	0.998	0.000
G90.3 Multisystem degeneration	0.000	0.998	0.002
I27.9 Pulmonary heart disease, unspecified	0.000	0.998	0.002
N36.1 Urethral diverticulum	0.002	0.998	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.001	0.998	0.000
Q39.8 Other congenital malformations of oesophagus	0.001	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.001	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.001	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.001	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.001	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.001	0.998	0.000
R41.2 Retrograde amnesia	0.002	0.998	0.000
Y79.2 Prosthetic and other implants, materials and accessory devices	0.002	0.998	0.000
N36 Other disorders of urethra	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.001	0.998	0.000
E10-E14 Diabetes mellitus	0.002	0.998	0.000
O20.9 Haemorrhage in early pregnancy, unspecified	0.002	0.998	0.000
D83.8 Other common variable immunodeficiencies	0.000	0.998	0.001
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells	0.000	0.998	0.001
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders	0.000	0.998	0.001
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function	0.000	0.998	0.001
Q39.4 Oesophageal web	0.001	0.998	0.000
N08 Glomerular disorders in diseases classified elsewhere	0.002	0.998	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.001	0.998	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.001	0.998	0.000
D43.0 Brain, supratentorial	0.002	0.998	0.000
L55.9 Sunburn, unspecified	0.000	0.998	0.001
L55.8 Other sunburn	0.000	0.998	0.001
L55.2 Sunburn of third degree	0.000	0.998	0.001
L55.1 Sunburn of second degree	0.000	0.998	0.001
L55.0 Sunburn of first degree	0.000	0.998	0.001
Chapter IV Endocrine, nutritional and metabolic diseases	0.002	0.998	0.000
D52.9 Folate deficiency anaemia, unspecified	0.000	0.998	0.001
D52.8 Other folate deficiency anaemias	0.000	0.998	0.001
D52.1 Drug-induced folate deficiency anaemia	0.000	0.998	0.001
D52.0 Dietary folate deficiency anaemia	0.000	0.998	0.001
D53.9 Nutritional anaemia, unspecified	0.000	0.998	0.001
S01.8 Open wound of other parts of head	0.000	0.998	0.002
D15.1 Heart	0.000	0.998	0.001
D53.8 Other specified nutritional anaemias	0.000	0.998	0.001
D53.2 Scorbutic anaemia	0.000	0.998	0.001
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.000	0.998	0.001
D53.0 Protein deficiency anaemia	0.000	0.998	0.001
G31.1 Senile degeneration of brain, not elsewhere classified	0.000	0.998	0.001
Q45.9 Congenital malformation of digestive system, unspecified	0.001	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.001	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.001	0.998	0.000
Q45.1 Annular pancreas	0.001	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.001	0.998	0.000
D84.1 Defects in the complement system	0.000	0.998	0.001
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.000	0.998	0.001
G04.9 Encephalitis, myelitis and encephalomyelitis, unspecified	0.000	0.998	0.001
L58.1 Chronic radiodermatitis	0.000	0.999	0.001
L58.0 Acute radiodermatitis	0.000	0.999	0.001
L59.8 Other specified disorders of skin and subcutaneous tissue related to radiation	0.000	0.999	0.001
L59.0 Erythema ab igne [dermatitis ab igne]	0.000	0.999	0.001
L85.9 Epidermal thickening, unspecified	0.001	0.999	0.000
F33.9 Recurrent depressive disorder, unspecified	0.001	0.999	0.000
F80.9 Developmental disorder of speech and language, unspecified	0.001	0.999	0.000
F80.8 Other developmental disorders of speech and language	0.001	0.999	0.000
F80.3 Acquired aphasia with epilepsy [Landau-Kleffner]	0.001	0.999	0.000
F80.2 Receptive language disorder	0.001	0.999	0.000
F80.0 Specific speech articulation disorder	0.001	0.999	0.000
N36.9 Urethral disorder, unspecified	0.001	0.999	0.000
Q40.2 Other specified congenital malformations of stomach	0.001	0.999	0.000
D56.3 Thalassaemia trait	0.000	0.999	0.001
D83.9 Common variable immunodeficiency, unspecified	0.000	0.999	0.001
L60.9 Nail disorder, unspecified	0.001	0.999	0.000
L89.3 Stage IV decubitus ulcer	0.001	0.999	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.999	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.999	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.001	0.999	0.000
Q40.1 Congenital hiatus hernia	0.001	0.999	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.001	0.999	0.000
R61.9 Hyperhidrosis, unspecified	0.000	0.999	0.001
E12 Malnutrition-related diabetes mellitus	0.001	0.999	0.000
H47.3 Other disorders of optic disk	0.000	0.999	0.001
L59.9 Disorder of skin and subcutaneous tissue related to radiation, unspecified	0.000	0.999	0.001
D84.8 Other specified immunodeficiencies	0.000	0.999	0.001
E26.0 Primary hyperaldosteronism	0.001	0.999	0.000
L58.9 Radiodermatitis, unspecified	0.000	0.999	0.001
N08.8 Glomerular disorders in other diseases classified elsewhere	0.001	0.999	0.000
N08.4 Glomerular disorders in other endocrine, nutritional and metabolic diseases	0.001	0.999	0.000
N08.2 Glomerular disorders in blood diseases and disorders involving the immune mechanism	0.001	0.999	0.000
N08.1 Glomerular disorders in neoplastic diseases	0.001	0.999	0.000
N08.0 Glomerular disorders in infectious and parasitic diseases classified elsewhere	0.001	0.999	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.001	0.999	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.001	0.999	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.001	0.999	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.001	0.999	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.001	0.999	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.001	0.999	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.001	0.999	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.001	0.999	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.001	0.999	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.001	0.999	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.001	0.999	0.000
S82.51 Fracture of medial malleolus (open)	0.000	0.999	0.001
H11.9 Disorder of conjunctiva, unspecified	0.000	0.999	0.001
I61.1 Intracerebral haemorrhage in hemisphere, cortical	0.001	0.999	0.000
D84.9 Immunodeficiency, unspecified	0.000	0.999	0.001
L60 Nail disorders	0.001	0.999	0.000
G04.8 Other encephalitis, myelitis and encephalomyelitis	0.000	0.999	0.001
K80 Cholelithiasis	0.001	0.999	0.000
S22.00 Fracture of thoracic vertebra (closed)	0.000	0.999	0.001
D86 Sarcoidosis	0.000	0.999	0.001
M24.47 Recurrent dislocation and subluxation of joint (Ankle and foot)	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