TreeWAS – Variant ID: rs7079041

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
F31 Bipolar affective disorder	0.000	0.821	0.179
F31.0 Bipolar affective disorder, current episode hypomanic	0.000	0.827	0.173
F31.9 Bipolar affective disorder, unspecified	0.000	0.833	0.167
F31.3 Bipolar affective disorder, current episode mild or moderate depression	0.000	0.834	0.166
F31.1 Bipolar affective disorder, current episode manic without psychotic symptoms	0.000	0.838	0.161
F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms	0.000	0.845	0.155
F31.4 Bipolar affective disorder, current episode severe depression without psychotic symptoms	0.000	0.849	0.151
F31.7 Bipolar affective disorder, currently in remission	0.000	0.859	0.141
F31.8 Other bipolar affective disorders	0.000	0.862	0.137
F31.6 Bipolar affective disorder, current episode mixed	0.000	0.871	0.129
F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms	0.000	0.878	0.122
Z08.9 Follow-up examination after unspecified treatment for malignant neoplasm	0.073	0.927	0.000
Z74.0 Reduced mobility	0.000	0.953	0.047
K74.6 Other and unspecified cirrhosis of liver	0.000	0.956	0.044
K74 Fibrosis and cirrhosis of liver	0.000	0.959	0.041
Z74 Problems related to care-provider dependency	0.000	0.964	0.036
Z74.2 Need for assistance at home and no other household member able to render care	0.000	0.964	0.036
K74.3 Primary biliary cirrhosis	0.000	0.964	0.036
K70-K77 Diseases of liver	0.000	0.965	0.035
K72.0 Acute and subacute hepatic failure	0.000	0.965	0.035
K72 Hepatic failure, not elsewhere classified	0.000	0.966	0.034
K75 Other inflammatory liver diseases	0.000	0.968	0.032
K70 Alcoholic liver disease	0.000	0.968	0.032
K74.5 Biliary cirrhosis, unspecified	0.000	0.969	0.031
K75.0 Abscess of liver	0.000	0.970	0.030
K74.4 Secondary biliary cirrhosis	0.000	0.970	0.029
K74.2 Hepatic fibrosis with hepatic sclerosis	0.000	0.970	0.029
K74.0 Hepatic fibrosis	0.000	0.971	0.029
K74.1 Hepatic sclerosis	0.000	0.972	0.028
K70.4 Alcoholic hepatic failure	0.000	0.972	0.028
Q20-Q28 Congenital malformations of the circulatory system	0.028	0.972	0.000
K72.1 Chronic hepatic failure	0.000	0.972	0.028
Q28 Other congenital malformations of circulatory system	0.027	0.973	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.027	0.973	0.000
K70.2 Alcoholic fibrosis and sclerosis of liver	0.000	0.973	0.027
Q28.2 Arteriovenous malformation of cerebral vessels	0.026	0.974	0.000
Q50-Q56 Congenital malformations of genital organs	0.026	0.974	0.000
Z74.3 Need for continuous supervision	0.000	0.974	0.026
Z74.1 Need for assistance with personal care	0.000	0.974	0.026
K75.4 Autoimmune hepatitis	0.000	0.974	0.026
Q21 Congenital malformations of cardiac septa	0.025	0.975	0.000
Q51 Congenital malformations of uterus and cervix	0.025	0.975	0.000
K70.3 Alcoholic cirrhosis of liver	0.000	0.975	0.025
K75.8 Other specified inflammatory liver diseases	0.000	0.975	0.025
Q00-Q07 Congenital malformations of the nervous system	0.025	0.975	0.000
Z74.9 Problem related to care-provider dependency, unspecified	0.000	0.976	0.024
K71 Toxic liver disease	0.000	0.976	0.024
K70.1 Alcoholic hepatitis	0.000	0.976	0.024
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.023	0.977	0.000
Q51.3 Bicornate uterus	0.023	0.977	0.000
K75.2 Nonspecific reactive hepatitis	0.000	0.977	0.023
K75.1 Phlebitis of portal vein	0.000	0.977	0.023
Q22 Congenital malformations of pulmonary and tricuspid valves	0.023	0.977	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.023	0.977	0.000
Z74.8 Other problems related to care-provider dependency	0.000	0.977	0.023
Q27 Other congenital malformations of peripheral vascular system	0.023	0.977	0.000
Q60-Q64 Congenital malformations of the urinary system	0.023	0.977	0.000
Q21.1 Atrial septal defect	0.023	0.977	0.000
Q05 Spina bifida	0.022	0.978	0.000
K75.3 Granulomatous hepatitis, not elsewhere classified	0.000	0.978	0.022
K77 Liver disorders in diseases classified elsewhere	0.000	0.978	0.022
Q21.9 Congenital malformation of cardiac septum, unspecified	0.022	0.978	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.022	0.978	0.000
Q51.8 Other congenital malformations of uterus and cervix	0.021	0.979	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.021	0.979	0.000
Q35-Q37 Cleft lip and cleft palate	0.021	0.979	0.000
Q52 Other congenital malformations of female genitalia	0.021	0.979	0.000
Q54 Hypospadias	0.021	0.979	0.000
K73 Chronic hepatitis, not elsewhere classified	0.000	0.979	0.021
Q25 Congenital malformations of great arteries	0.021	0.979	0.000
Q26 Congenital malformations of great veins	0.021	0.979	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.021	0.979	0.000
Q03 Congenital hydrocephalus	0.020	0.980	0.000
Q23 Congenital malformations of aortic and mitral valves	0.020	0.980	0.000
Q27.3 Peripheral arteriovenous malformation	0.020	0.980	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.020	0.980	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.020	0.980	0.000
Q28.1 Other malformations of precerebral vessels	0.020	0.980	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.020	0.980	0.000
Q90 Down's syndrome	0.019	0.980	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.019	0.981	0.000
Q05.9 Spina bifida, unspecified	0.019	0.981	0.000
Q51.1 Doubling of uterus with doubling of cervix and vagina	0.019	0.981	0.000
Q53 Undescended testicle	0.019	0.981	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.019	0.981	0.000
Q28.3 Other malformations of cerebral vessels	0.019	0.981	0.000
Q51.4 Unicornate uterus	0.019	0.981	0.000
Q22.5 Ebstein's anomaly	0.019	0.981	0.000
Q55 Other congenital malformations of male genital organs	0.019	0.981	0.000
Q05.7 Lumbar spina bifida without hydrocephalus	0.019	0.981	0.000
Q51.2 Other doubling of uterus	0.019	0.981	0.000
K70.9 Alcoholic liver disease, unspecified	0.000	0.981	0.019
K70.0 Alcoholic fatty liver	0.000	0.981	0.018
K76 Other diseases of liver	0.000	0.981	0.019
Q21.8 Other congenital malformations of cardiac septa	0.018	0.981	0.000
Q21.4 Aortopulmonary septal defect	0.018	0.981	0.000
Q21.2 Atrioventricular septal defect	0.018	0.981	0.000
Q51.9 Congenital malformation of uterus and cervix, unspecified	0.018	0.982	0.000
Q51.7 Congenital fistulae between uterus and digestive and urinary tracts	0.018	0.982	0.000
Q51.6 Embryonic cyst of cervix	0.018	0.982	0.000
Q51.5 Agenesis and aplasia of cervix	0.018	0.982	0.000
Q51.0 Agenesis and aplasia of uterus	0.018	0.982	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.018	0.982	0.000
Q40 Other congenital malformations of upper alimentary tract	0.018	0.982	0.000
Q04 Other congenital malformations of brain	0.018	0.982	0.000
Q06 Other congenital malformations of spinal cord	0.018	0.982	0.000
Q01 Encephalocele	0.018	0.982	0.000
Q00 Anencephaly and similar malformations	0.018	0.982	0.000
Q02 Microcephaly	0.018	0.982	0.000
Q38.7 Pharyngeal pouch	0.018	0.982	0.000
Q64 Other congenital malformations of urinary system	0.018	0.982	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.017	0.982	0.000
Q21.3 Tetralogy of Fallot	0.017	0.982	0.000
Q52.5 Fusion of labia	0.017	0.982	0.000
Q54.9 Hypospadias, unspecified	0.017	0.982	0.000
K71.9 Toxic liver disease, unspecified	0.000	0.982	0.017
K71.8 Toxic liver disease with other disorders of liver	0.000	0.982	0.017
K71.7 Toxic liver disease with fibrosis and cirrhosis of liver	0.000	0.982	0.017
K71.5 Toxic liver disease with chronic active hepatitis	0.000	0.982	0.017
K71.4 Toxic liver disease with chronic lobular hepatitis	0.000	0.982	0.017
K71.3 Toxic liver disease with chronic persistent hepatitis	0.000	0.982	0.017
K71.2 Toxic liver disease with acute hepatitis	0.000	0.982	0.017
Q14 Congenital malformations of posterior segment of eye	0.017	0.983	0.000
Q07 Other congenital malformations of nervous system	0.017	0.983	0.000
K71.6 Toxic liver disease with hepatitis, not elsewhere classified	0.000	0.983	0.017
Q96 Turner's syndrome	0.017	0.983	0.000
Q54.8 Other hypospadias	0.017	0.983	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.017	0.983	0.000
K71.1 Toxic liver disease with hepatic necrosis	0.000	0.983	0.017
Q03.0 Malformations of aqueduct of Sylvius	0.017	0.983	0.000
Q90.9 Down's syndrome, unspecified	0.017	0.983	0.000
Q24 Other congenital malformations of heart	0.017	0.983	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.017	0.983	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.017	0.983	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.017	0.983	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.017	0.983	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.017	0.983	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.017	0.983	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.017	0.983	0.000
Q63 Other congenital malformations of kidney	0.017	0.983	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.016	0.983	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.016	0.983	0.000
Q22.6 Hypoplastic right heart syndrome	0.016	0.983	0.000
Q22.4 Congenital tricuspid stenosis	0.016	0.983	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.016	0.983	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.016	0.983	0.000
Q22.1 Congenital pulmonary valve stenosis	0.016	0.983	0.000
Q22.0 Pulmonary valve atresia	0.016	0.983	0.000
Q23.3 Congenital mitral insufficiency	0.017	0.983	0.000
K71.0 Toxic liver disease with cholestasis	0.000	0.983	0.016
K76.8 Other specified diseases of liver	0.000	0.983	0.017
Q25.0 Patent ductus arteriosus	0.016	0.983	0.000
Q27.4 Congenital phlebectasia	0.016	0.983	0.000
Q27.2 Other congenital malformations of renal artery	0.016	0.983	0.000
Q27.1 Congenital renal artery stenosis	0.016	0.983	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.016	0.983	0.000
Q37 Cleft palate with cleft lip	0.016	0.983	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.016	0.984	0.000
Q05.8 Sacral spina bifida without hydrocephalus	0.016	0.984	0.000
Q05.6 Thoracic spina bifida without hydrocephalus	0.016	0.984	0.000
Q05.5 Cervical spina bifida without hydrocephalus	0.016	0.984	0.000
Q05.4 Unspecified spina bifida with hydrocephalus	0.016	0.984	0.000
Q05.3 Sacral spina bifida with hydrocephalus	0.016	0.984	0.000
Q05.2 Lumbar spina bifida with hydrocephalus	0.016	0.984	0.000
Q05.1 Thoracic spina bifida with hydrocephalus	0.016	0.984	0.000
Q05.0 Cervical spina bifida with hydrocephalus	0.016	0.984	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.016	0.984	0.000
Q21.0 Ventricular septal defect	0.016	0.984	0.000
Q61 Cystic kidney disease	0.016	0.984	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.016	0.984	0.000
K77.0 Liver disorders in infectious and parasitic diseases classified elsewhere	0.000	0.984	0.016
Q15 Other congenital malformations of eye	0.016	0.984	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.016	0.984	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.016	0.984	0.000
Q80-Q89 Other congenital malformations	0.016	0.984	0.000
Q35 Cleft palate	0.016	0.984	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.016	0.984	0.000
Q17 Other congenital malformations of ear	0.016	0.984	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.015	0.984	0.000
Q13 Congenital malformations of anterior segment of eye	0.015	0.984	0.000
Q36 Cleft lip	0.015	0.984	0.000
Q52.9 Congenital malformation of female genitalia, unspecified	0.015	0.985	0.000
Q52.8 Other specified congenital malformations of female genitalia	0.015	0.985	0.000
Q52.7 Other congenital malformations of vulva	0.015	0.985	0.000
Q52.6 Congenital malformation of clitoris	0.015	0.985	0.000
Q52.4 Other congenital malformations of vagina	0.015	0.985	0.000
Q52.3 Imperforate hymen	0.015	0.985	0.000
Q52.2 Congenital rectovaginal fistula	0.015	0.985	0.000
Q52.0 Congenital absence of vagina	0.015	0.985	0.000
L89.1 Stage II decubitus ulcer	0.000	0.985	0.015
Q52.1 Doubling of vagina	0.015	0.985	0.000
K75.9 Inflammatory liver disease, unspecified	0.000	0.985	0.015
Q54.4 Congenital chordee	0.015	0.985	0.000
Q54.3 Hypospadias, perineal	0.015	0.985	0.000
Q54.2 Hypospadias, penoscrotal	0.015	0.985	0.000
K73.8 Other chronic hepatitis, not elsewhere classified	0.000	0.985	0.015
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.015	0.985	0.000
K73.1 Chronic lobular hepatitis, not elsewhere classified	0.000	0.985	0.015
K73.0 Chronic persistent hepatitis, not elsewhere classified	0.000	0.985	0.015
S82.80 Fractures of other parts of lower leg (closed)	0.000	0.985	0.015
Q25.9 Congenital malformation of great arteries, unspecified	0.015	0.985	0.000
Q25.8 Other congenital malformations of great arteries	0.015	0.985	0.000
Q25.5 Atresia of pulmonary artery	0.015	0.985	0.000
Q25.3 Stenosis of aorta	0.015	0.985	0.000
Q25.2 Atresia of aorta	0.015	0.985	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.015	0.985	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.015	0.985	0.000
Q20.6 Isomerism of atrial appendages	0.015	0.985	0.000
Q20.5 Discordant atrioventricular connexion	0.015	0.985	0.000
Q20.4 Double inlet ventricle	0.015	0.985	0.000
Q20.3 Discordant ventriculoarterial connexion	0.015	0.985	0.000
Q20.2 Double outlet left ventricle	0.015	0.985	0.000
Q20.1 Double outlet right ventricle	0.015	0.985	0.000
Q20.0 Common arterial trunk	0.015	0.985	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.015	0.985	0.000
Q26.8 Other congenital malformations of great veins	0.015	0.985	0.000
Q26.6 Portal vein-hepatic artery fistula	0.015	0.985	0.000
Q26.5 Anomalous portal venous connexion	0.015	0.985	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.015	0.985	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.015	0.985	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.015	0.985	0.000
Q26.1 Persistent left superior vena cava	0.015	0.985	0.000
Q26.0 Congenital stenosis of vena cava	0.015	0.985	0.000
Q03.9 Congenital hydrocephalus, unspecified	0.015	0.985	0.000
Q03.8 Other congenital hydrocephalus	0.015	0.985	0.000
Q03.1 Atresia of foramina of Magendie and Luschka	0.015	0.985	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.015	0.985	0.000
Q18 Other congenital malformations of face and neck	0.015	0.985	0.000
Q30 Congenital malformations of nose	0.015	0.985	0.000
Q40.2 Other specified congenital malformations of stomach	0.015	0.985	0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.015	0.985	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.015	0.985	0.000
Q23.4 Hypoplastic left heart syndrome	0.015	0.985	0.000
Q23.2 Congenital mitral stenosis	0.015	0.985	0.000
Q43 Other congenital malformations of intestine	0.015	0.985	0.000
Q14.1 Congenital malformation of retina	0.015	0.985	0.000
Q62.5 Duplication of ureter	0.015	0.985	0.000
Q45 Other congenital malformations of digestive system	0.014	0.985	0.000
Q63.0 Accessory kidney	0.015	0.985	0.000
K76.6 Portal hypertension	0.000	0.986	0.014
Q62.2 Congenital megaloureter	0.014	0.986	0.000
Q34 Other congenital malformations of respiratory system	0.014	0.986	0.000
Q33 Congenital malformations of lung	0.014	0.986	0.000
Q32 Congenital malformations of trachea and bronchus	0.014	0.986	0.000
Q23.1 Congenital insufficiency of aortic valve	0.014	0.986	0.000
Q44.4 Choledochal cyst	0.014	0.986	0.000
Q25.6 Stenosis of pulmonary artery	0.014	0.986	0.000
Q90.2 Trisomy 21, translocation	0.014	0.986	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.014	0.986	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.014	0.986	0.000
Q38.8 Other congenital malformations of pharynx	0.014	0.986	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.014	0.986	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.014	0.986	0.000
Q38.3 Other congenital malformations of tongue	0.014	0.986	0.000
Q38.2 Macroglossia	0.014	0.986	0.000
Q38.1 Ankyloglossia	0.014	0.986	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.014	0.986	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.014	0.986	0.000
Q40.1 Congenital hiatus hernia	0.014	0.986	0.000
Q53.9 Undescended testicle, unspecified	0.014	0.986	0.000
Q54.1 Hypospadias, penile	0.014	0.986	0.000
Q55.0 Absence and aplasia of testis	0.014	0.986	0.000
K73.9 Chronic hepatitis, unspecified	0.000	0.986	0.014
Q89 Other congenital malformations, not elsewhere classified	0.014	0.986	0.000
Q25.4 Other congenital malformations of aorta	0.014	0.986	0.000
Q53.2 Undescended testicle, bilateral	0.014	0.986	0.000
Q53.0 Ectopic testis	0.014	0.986	0.000
Q56.4 Indeterminate sex, unspecified	0.014	0.986	0.000
Q56.3 Pseudohermaphroditism, unspecified	0.014	0.986	0.000
Q56.2 Female pseudohermaphroditism, not elsewhere classified	0.014	0.986	0.000
Q56.1 Male pseudohermaphroditism, not elsewhere classified	0.014	0.986	0.000
Q56.0 Hermaphroditism, not elsewhere classified	0.014	0.986	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.014	0.986	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.014	0.986	0.000
Q55.6 Other congenital malformations of penis	0.014	0.986	0.000
Q04.8 Other specified congenital malformations of brain	0.014	0.986	0.000
Q55.9 Congenital malformation of male genital organ, unspecified	0.014	0.986	0.000
Q55.8 Other specified congenital malformations of male genital organs	0.014	0.986	0.000
Q55.5 Congenital absence and aplasia of penis	0.014	0.986	0.000
Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate	0.014	0.986	0.000
Q55.3 Atresia of vas deferens	0.014	0.986	0.000
Q55.1 Hypoplasia of testis and scrotum	0.014	0.986	0.000
Q31 Congenital malformations of larynx	0.014	0.986	0.000
Q61.0 Congenital single renal cyst	0.014	0.986	0.000
Q54.0 Hypospadias, balanic	0.014	0.986	0.000
Q53.1 Undescended testicle, unilateral	0.014	0.986	0.000
Q61.3 Polycystic kidney, unspecified	0.014	0.986	0.000
K76.5 Hepatic veno-occlusive disease	0.000	0.986	0.013
K76.4 Peliosis hepatis	0.000	0.986	0.013
K76.3 Infarction of liver	0.000	0.986	0.013
K76.2 Central haemorrhagic necrosis of liver	0.000	0.986	0.013
Q62.8 Other congenital malformations of ureter	0.013	0.986	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.013	0.986	0.000
Q62.6 Malposition of ureter	0.013	0.986	0.000
Q62.4 Agenesis of ureter	0.013	0.986	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.013	0.986	0.000
Q62.1 Atresia and stenosis of ureter	0.013	0.986	0.000
Q62.0 Congenital hydronephrosis	0.013	0.986	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.013	0.987	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.013	0.987	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.013	0.987	0.000
Q44.7 Other congenital malformations of liver	0.013	0.987	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.013	0.987	0.000
Q38.6 Other congenital malformations of mouth	0.013	0.987	0.000
Q04.9 Congenital malformation of brain, unspecified	0.013	0.987	0.000
Q04.5 Megalencephaly	0.013	0.987	0.000
Q04.4 Septo-optic dysplasia	0.013	0.987	0.000
Q04.3 Other reduction deformities of brain	0.013	0.987	0.000
Q04.2 Holoprosencephaly	0.013	0.987	0.000
Q04.1 Arhinencephaly	0.013	0.987	0.000
Q04.0 Congenital malformations of corpus callosum	0.013	0.987	0.000
K76.7 Hepatorenal syndrome	0.000	0.987	0.013
Q63.8 Other specified congenital malformations of kidney	0.013	0.987	0.000
Q00.2 Iniencephaly	0.013	0.987	0.000
Q00.1 Craniorachischisis	0.013	0.987	0.000
Q00.0 Anencephaly	0.013	0.987	0.000
Q01.9 Encephalocele, unspecified	0.013	0.987	0.000
Q01.8 Encephalocele of other sites	0.013	0.987	0.000
Q01.2 Occipital encephalocele	0.013	0.987	0.000
Q01.1 Nasofrontal encephalocele	0.013	0.987	0.000
Q01.0 Frontal encephalocele	0.013	0.987	0.000
Q06.9 Congenital malformation of spinal cord, unspecified	0.013	0.987	0.000
Q06.8 Other specified congenital malformations of spinal cord	0.013	0.987	0.000
Q06.4 Hydromyelia	0.013	0.987	0.000
Q06.3 Other congenital cauda equina malformations	0.013	0.987	0.000
Q06.2 Diastematomyelia	0.013	0.987	0.000
Q06.1 Hypoplasia and dysplasia of spinal cord	0.013	0.987	0.000
Q06.0 Amyelia	0.013	0.987	0.000
Q96.9 Turner's syndrome, unspecified	0.013	0.987	0.000
Q37.9 Unspecified cleft palate with unilateral cleft lip	0.013	0.987	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.013	0.987	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.013	0.987	0.000
Q64.8 Other specified congenital malformations of urinary system	0.013	0.987	0.000
Q64.6 Congenital diverticulum of bladder	0.013	0.987	0.000
Q64.5 Congenital absence of bladder and urethra	0.013	0.987	0.000
Q64.4 Malformation of urachus	0.013	0.987	0.000
Q64.2 Congenital posterior urethral valves	0.013	0.987	0.000
Q64.1 Exstrophy of urinary bladder	0.013	0.987	0.000
Q64.0 Epispadias	0.013	0.987	0.000
Q04.6 Congenital cerebral cysts	0.013	0.987	0.000
F43.2 Adjustment disorders	0.013	0.987	0.000
Q61.9 Cystic kidney disease, unspecified	0.013	0.987	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.013	0.987	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.013	0.987	0.000
Q98.7 Male with sex chromosome mosaicism	0.013	0.987	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.013	0.987	0.000
Q98.5 Karyotype 47,XYY	0.013	0.987	0.000
Q98.3 Other male with 46,XX karyotype	0.013	0.987	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.013	0.987	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.013	0.987	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.013	0.987	0.000
Q10.0 Congenital ptosis	0.013	0.987	0.000
K72.9 Hepatic failure, unspecified	0.000	0.987	0.013
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.013	0.987	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.013	0.987	0.000
Q14.3 Congenital malformation of choroid	0.013	0.987	0.000
Q14.2 Congenital malformation of optic disk	0.013	0.987	0.000
Q14.0 Congenital malformation of vitreous humour	0.013	0.987	0.000
Q24.5 Malformation of coronary vessels	0.013	0.987	0.000
Q07.9 Congenital malformation of nervous system, unspecified	0.012	0.987	0.000
Q07.8 Other specified congenital malformations of nervous system	0.012	0.987	0.000
K77.8 Liver disorders in other diseases classified elsewhere	0.001	0.987	0.012
Q89.2 Congenital malformations of other endocrine glands	0.013	0.987	0.000
Q96.8 Other variants of Turner's syndrome	0.012	0.987	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.012	0.987	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.012	0.987	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.012	0.987	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.012	0.987	0.000
Q96.0 Karyotype 45,X	0.012	0.987	0.000
F43 Reaction to severe stress, and adjustment disorders	0.013	0.987	0.000
Q25.1 Coarctation of aorta	0.012	0.987	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.012	0.987	0.000
Q44.2 Atresia of bile ducts	0.012	0.987	0.000
Q44.1 Other congenital malformations of gallbladder	0.012	0.987	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.012	0.987	0.000
Q11.1 Other anophthalmos	0.012	0.987	0.000
Q24.4 Congenital subaortic stenosis	0.012	0.988	0.000
Q24.3 Pulmonary infundibular stenosis	0.012	0.988	0.000
Q24.2 Cor triatriatum	0.012	0.988	0.000
Q24.1 Levocardia	0.012	0.988	0.000
Q12 Congenital lens malformations	0.012	0.988	0.000
Q18.1 Preauricular sinus and cyst	0.012	0.988	0.000
Q15.0 Congenital glaucoma	0.012	0.988	0.000
Q91.7 Patau's syndrome, unspecified	0.012	0.988	0.000
Q91.6 Trisomy 13, translocation	0.012	0.988	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.012	0.988	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.012	0.988	0.000
Q91.3 Edwards' syndrome, unspecified	0.012	0.988	0.000
Q91.2 Trisomy 18, translocation	0.012	0.988	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.012	0.988	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.012	0.988	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.012	0.988	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.012	0.988	0.000
Q92.7 Triploidy and polyploidy	0.012	0.988	0.000
Q92.6 Extra marker chromosomes	0.012	0.988	0.000
Q92.5 Duplications with other complex rearrangements	0.012	0.988	0.000
Q92.4 Duplications seen only at prometaphase	0.012	0.988	0.000
Q92.3 Minor partial trisomy	0.012	0.988	0.000
Q92.2 Major partial trisomy	0.012	0.988	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.012	0.988	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.012	0.988	0.000
Q93.9 Deletion from autosomes, unspecified	0.012	0.988	0.000
Q93.8 Other deletions from the autosomes	0.012	0.988	0.000
Q93.7 Deletions with other complex rearrangements	0.012	0.988	0.000
Q93.6 Deletions seen only at prometaphase	0.012	0.988	0.000
Q93.5 Other deletions of part of a chromosome	0.012	0.988	0.000
Q93.4 Deletion of short arm of chromosome 5	0.012	0.988	0.000
Q93.3 Deletion of short arm of chromosome 4	0.012	0.988	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.012	0.988	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.012	0.988	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.012	0.988	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.012	0.988	0.000
Q95.8 Other balanced rearrangements and structural markers	0.012	0.988	0.000
Q95.5 Individuals with autosomal fragile site	0.012	0.988	0.000
Q95.4 Individuals with marker heterochromatin	0.012	0.988	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.012	0.988	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.012	0.988	0.000
Q95.1 Chromosome inversion in normal individual	0.012	0.988	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.012	0.988	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.012	0.988	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.012	0.988	0.000
Q97.3 Female with 46,XY karyotype	0.012	0.988	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.012	0.988	0.000
Q97.1 Female with more than three X chromosomes	0.012	0.988	0.000
Q97.0 Karyotype 47,XXX	0.012	0.988	0.000
Q99.9 Chromosomal abnormality, unspecified	0.012	0.988	0.000
Q99.8 Other specified chromosome abnormalities	0.012	0.988	0.000
Q99.2 Fragile X chromosome	0.012	0.988	0.000
Q99.1 46,XX true hermaphrodite	0.012	0.988	0.000
Q99.0 Chimera 46,XX/46,XY	0.012	0.988	0.000
Q83 Congenital malformations of breast	0.012	0.988	0.000
K76.1 Chronic passive congestion of liver	0.000	0.988	0.012
Q63.9 Congenital malformation of kidney, unspecified	0.012	0.988	0.000
Q63.3 Hyperplastic and giant kidney	0.012	0.988	0.000
F43.9 Reaction to severe stress, unspecified	0.012	0.988	0.000
Q24.6 Congenital heart block	0.012	0.988	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.012	0.988	0.000
Q37.8 Unspecified cleft palate with bilateral cleft lip	0.012	0.988	0.000
Q37.5 Cleft hard and soft palate with unilateral cleft lip	0.012	0.988	0.000
Q37.4 Cleft hard and soft palate with bilateral cleft lip	0.012	0.988	0.000
Q37.3 Cleft soft palate with unilateral cleft lip	0.012	0.988	0.000
Q37.2 Cleft soft palate with bilateral cleft lip	0.012	0.988	0.000
Q37.1 Cleft hard palate with unilateral cleft lip	0.012	0.988	0.000
Q37.0 Cleft hard palate with bilateral cleft lip	0.012	0.988	0.000
K73.2 Chronic active hepatitis, not elsewhere classified	0.000	0.988	0.012
Q35.9 Cleft palate, unspecified	0.012	0.988	0.000
Q10.7 Congenital malformation of orbit	0.012	0.988	0.000
Q10.6 Other congenital malformations of lachrymal apparatus	0.012	0.988	0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct	0.012	0.988	0.000
Q10.4 Absence and agenesis of lachrymal apparatus	0.012	0.988	0.000
Q10.3 Other congenital malformations of eyelid	0.012	0.988	0.000
Q10.2 Congenital entropion	0.012	0.988	0.000
Q10.1 Congenital ectropion	0.012	0.988	0.000
Q23.0 Congenital stenosis of aortic valve	0.012	0.988	0.000
Q61.8 Other cystic kidney diseases	0.012	0.988	0.000
Q61.1 Polycystic kidney, infantile type	0.012	0.988	0.000
Q61.4 Renal dysplasia	0.012	0.988	0.000
Q07.0 Arnold-Chiari syndrome	0.012	0.988	0.000
Q11.3 Macrophthalmos	0.012	0.988	0.000
Q11.2 Microphthalmos	0.012	0.988	0.000
Q11.0 Cystic eyeball	0.012	0.988	0.000
Q15.9 Congenital malformation of eye, unspecified	0.012	0.988	0.000
Q15.8 Other specified congenital malformations of eye	0.012	0.988	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.012	0.988	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.012	0.988	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.012	0.988	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.012	0.988	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.012	0.988	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.012	0.988	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.012	0.988	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.012	0.988	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.012	0.988	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.012	0.988	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.012	0.988	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.012	0.988	0.000
Q43.3 Congenital malformations of intestinal fixation	0.012	0.988	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.012	0.988	0.000
Q84 Other congenital malformations of integument	0.012	0.988	0.000
Q81 Epidermolysis bullosa	0.012	0.988	0.000
Q80 Congenital ichthyosis	0.012	0.988	0.000
Q17.5 Prominent ear	0.011	0.988	0.000
Q35.8 (Cleft palate, unspecified, bilateral)	0.011	0.988	0.000
Q35.7 Cleft uvula	0.011	0.988	0.000
Q35.6 Cleft palate, medial	0.011	0.988	0.000
Q35.5 Cleft hard palate with cleft soft palate	0.011	0.988	0.000
Q35.4 (Cleft hard palate with cleft soft palate, bilateral)	0.011	0.988	0.000
Q35.3 Cleft soft palate	0.011	0.988	0.000
Q35.2 (Cleft soft palate, bilateral)	0.011	0.988	0.000
Q35.1 Cleft hard palate	0.011	0.988	0.000
Q35.0 (Cleft hard palate, bilateral)	0.011	0.988	0.000
Q60.6 Potter's syndrome	0.011	0.988	0.000
Q60.5 Renal hypoplasia, unspecified	0.011	0.988	0.000
Q60.4 Renal hypoplasia, bilateral	0.011	0.988	0.000
Q60.3 Renal hypoplasia, unilateral	0.011	0.988	0.000
Q60.2 Renal agenesis, unspecified	0.012	0.988	0.000
Q60.1 Renal agenesis, bilateral	0.011	0.988	0.000
Q24.0 Dextrocardia	0.011	0.988	0.000
Q44.5 Other congenital malformations of bile ducts	0.011	0.988	0.000
Q17.9 Congenital malformation of ear, unspecified	0.011	0.988	0.000
Q17.8 Other specified congenital malformations of ear	0.011	0.988	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