TreeWAS – Variant ID: rs10971721

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
I63.9 Cerebral infarction, unspecified	0.052	0.948	0.000
Y83.2 Surgical operation with anastomosis, bypass or graft	0.022	0.978	0.000
O36.8 Maternal care for other specified foetal problems	0.000	0.980	0.020
N95.0 Postmenopausal bleeding	0.000	0.981	0.019
O36 Maternal care for other known or suspected foetal problems	0.000	0.982	0.018
O36.0 Maternal care for rhesus isoimmunisation	0.000	0.982	0.018
O36.9 Maternal care for foetal problem, unspecified	0.000	0.983	0.017
O36.6 Maternal care for excessive foetal growth	0.000	0.984	0.016
O36.3 Maternal care for signs of foetal hypoxia	0.000	0.985	0.014
O36.7 Maternal care for viable foetus in abdominal pregnancy	0.000	0.986	0.013
O36.2 Maternal care for hydrops foetalis	0.000	0.986	0.013
O36.5 Maternal care for poor foetal growth	0.000	0.987	0.013
O36.1 Maternal care for other isoimmunisation	0.000	0.988	0.012
O36.4 Maternal care for intra-uterine death	0.000	0.988	0.012
D69.6 Thrombocytopenia, unspecified	0.010	0.990	0.000
N95 Menopausal and other perimenopausal disorders	0.000	0.990	0.010
D69.3 Idiopathic thrombocytopenic purpura	0.009	0.991	0.000
D69 Purpura and other haemorrhagic conditions	0.009	0.991	0.000
N95.2 Postmenopausal atrophic vaginitis	0.000	0.992	0.008
N95.1 Menopausal and female climacteric states	0.000	0.992	0.008
C18.9 Colon, unspecified	0.008	0.992	0.000
N95.3 States associated with artificial menopause	0.000	0.992	0.008
D69.2 Other nonthrombocytopenic purpura	0.008	0.992	0.000
N95.9 Menopausal and perimenopausal disorder, unspecified	0.000	0.993	0.007
O47.1 False labour at or after 37 completed weeks of gestation	0.000	0.993	0.007
I63 Cerebral infarction	0.007	0.993	0.000
C18.2 Ascending colon	0.007	0.993	0.000
N95.8 Other specified menopausal and perimenopausal disorders	0.000	0.993	0.007
D69.4 Other primary thrombocytopenia	0.007	0.993	0.000
D69.8 Other specified haemorrhagic conditions	0.006	0.993	0.000
D69.1 Qualitative platelet defects	0.006	0.993	0.000
D69.0 Allergic purpura	0.006	0.994	0.000
C18 Malignant neoplasm of colon	0.006	0.994	0.000
D69.9 Haemorrhagic condition, unspecified	0.006	0.994	0.000
C18.3 Hepatic flexure	0.006	0.994	0.000
D69.5 Secondary thrombocytopenia	0.005	0.994	0.000
C18.0 Caecum	0.005	0.995	0.000
I63.6 Cerebral infarction due to cerebral venous thrombosis, nonpyogenic	0.005	0.995	0.000
I63.1 Cerebral infarction due to embolism of precerebral arteries	0.005	0.995	0.000
I63.0 Cerebral infarction due to thrombosis of precerebral arteries	0.005	0.995	0.000
M10.99 Gout, unspecified (Site unspecified)	0.000	0.995	0.005
I63.3 Cerebral infarction due to thrombosis of cerebral arteries	0.005	0.995	0.000
C18.1 Appendix	0.005	0.995	0.000
H20.9 Iridocyclitis, unspecified	0.000	0.995	0.005
I63.4 Cerebral infarction due to embolism of cerebral arteries	0.005	0.995	0.000
C18.4 Transverse colon	0.005	0.995	0.000
C18.8 Overlapping lesion of colon	0.004	0.995	0.000
I63.2 Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries	0.004	0.995	0.000
R16.1 Splenomegaly, not elsewhere classified	0.005	0.995	0.000
C18.5 Splenic flexure	0.004	0.996	0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.004	0.996	0.000
D68.8 Other specified coagulation defects	0.004	0.996	0.000
H83.0 Labyrinthitis	0.004	0.996	0.000
I63.8 Other cerebral infarction	0.004	0.996	0.000
J33.9 Nasal polyp, unspecified	0.000	0.996	0.004
O47 False labour	0.000	0.996	0.004
H20 Iridocyclitis	0.000	0.996	0.004
R27.8 Other and unspecified lack of coordination	0.004	0.996	0.000
D68 Other coagulation defects	0.004	0.996	0.000
O47.9 False labour, unspecified	0.000	0.996	0.004
H20.8 Other iridocyclitis	0.000	0.996	0.004
I44.0 Atrioventricular block, first degree	0.000	0.996	0.004
R63.0 Anorexia	0.000	0.996	0.004
D67 Hereditary factor IX deficiency	0.003	0.997	0.000
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.003	0.997	0.000
C18.6 Descending colon	0.003	0.997	0.000
I69.4 Sequelae of stroke, not specified as haemorrhage or infarction	0.003	0.997	0.000
D68.0 Von Willebrand's disease	0.003	0.997	0.000
H20.0 Acute and subacute iridocyclitis	0.000	0.997	0.003
H18.5 Hereditary corneal dystrophies	0.000	0.997	0.003
Z47.0 Follow-up care involving removal of fracture plate and other internal fixation device	0.003	0.997	0.000
H20.2 Lens-induced iridocyclitis	0.000	0.997	0.003
H20.1 Chronic iridocyclitis	0.000	0.997	0.003
R44.3 Hallucinations, unspecified	0.000	0.997	0.003
D68.1 Hereditary factor XI deficiency	0.003	0.997	0.000
D68.5 Primary Thrombophilia	0.003	0.997	0.000
D68.3 Haemorrhagic disorder due to circulating anticoagulants	0.003	0.997	0.000
H18 Other disorders of cornea	0.000	0.997	0.003
H16.0 Corneal ulcer	0.000	0.997	0.003
I63.5 Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries	0.003	0.997	0.000
D68.4 Acquired coagulation factor deficiency	0.003	0.997	0.000
H18.4 Corneal degeneration	0.000	0.997	0.003
D66 Hereditary factor VIII deficiency	0.003	0.997	0.000
D68.6 Other Thrombophilia	0.003	0.997	0.000
H15-H22 Disorders of sclera, cornea, iris and ciliary body	0.000	0.997	0.003
O47.0 False labour before 37 completed weeks of gestation	0.000	0.997	0.003
Q82.8 Other specified congenital malformations of skin	0.003	0.997	0.000
H16 Keratitis	0.000	0.997	0.003
R27.0 Ataxia, unspecified	0.003	0.997	0.000
F17.2 Dependence syndrome	0.003	0.997	0.000
N93.0 Postcoital and contact bleeding	0.003	0.997	0.000
R44.1 Visual hallucinations	0.000	0.997	0.003
I69 Sequelae of cerebrovascular disease	0.003	0.997	0.000
R27 Other lack of coordination	0.003	0.997	0.000
Q07.0 Arnold-Chiari syndrome	0.003	0.997	0.000
R44.8 Other and unspecified symptoms and signs involving general sensations and perceptions	0.000	0.997	0.003
R44 Other symptoms and signs involving general sensations and perceptions	0.000	0.997	0.003
H83 Other diseases of inner ear	0.003	0.997	0.000
H18.9 Disorder of cornea, unspecified	0.000	0.997	0.002
M81.40 Drug-induced osteoporosis (Multiple sites)	0.002	0.998	0.000
H18.7 Other corneal deformities	0.000	0.998	0.002
H18.3 Changes in corneal membranes	0.000	0.998	0.002
H18.2 Other corneal oedema	0.000	0.998	0.002
H18.0 Corneal pigmentations and deposits	0.000	0.998	0.002
Q82 Other congenital malformations of skin	0.002	0.998	0.000
H18.1 Bullous keratopathy	0.000	0.998	0.002
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
O34.7 Maternal care for abnormality of vulva and perineum	0.002	0.998	0.000
H17 Corneal scars and opacities	0.000	0.998	0.002
H16.9 Keratitis, unspecified	0.000	0.998	0.002
Q43.8 Other specified congenital malformations of intestine	0.002	0.998	0.000
Q43 Other congenital malformations of intestine	0.002	0.998	0.000
H18.8 Other specified disorders of cornea	0.000	0.998	0.002
M19.94 Arthrosis, unspecified (Hand)	0.000	0.998	0.002
D68.9 Coagulation defect, unspecified	0.002	0.998	0.000
Q63.0 Accessory kidney	0.002	0.998	0.000
H15 Disorders of sclera	0.000	0.998	0.002
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
I60-I69 Cerebrovascular diseases	0.002	0.998	0.000
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
H25.9 Senile cataract, unspecified	0.000	0.998	0.002
I69.8 Sequelae of other and unspecified cerebrovascular diseases	0.002	0.998	0.000
I69.0 Sequelae of subarachnoid haemorrhage	0.002	0.998	0.000
N43.3 Hydrocele, unspecified	0.000	0.998	0.002
R90.8 Other abnormal findings on diagnostic imaging of central nervous system	0.002	0.998	0.000
H16.8 Other keratitis	0.000	0.998	0.002
H16.4 Corneal neovascularisation	0.000	0.998	0.002
H16.3 Interstitial and deep keratitis	0.000	0.998	0.002
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
H44.2 Degenerative myopia	0.000	0.998	0.002
R44.0 Auditory hallucinations	0.000	0.998	0.002
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
H18.6 Keratoconus	0.000	0.998	0.002
H22 Disorders of iris and ciliary body in diseases classified elsewhere	0.000	0.998	0.002
I69.2 Sequelae of other nontraumatic intracranial haemorrhage	0.002	0.998	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.002	0.998	0.000
H83.8 Other specified diseases of inner ear	0.002	0.998	0.000
R44.2 Other hallucinations	0.000	0.998	0.002
H83.9 Disease of inner ear, unspecified	0.002	0.998	0.000
H83.3 Noise effects on inner ear	0.002	0.998	0.000
H83.2 Labyrinthine dysfunction	0.002	0.998	0.000
H83.1 Labyrinthine fistula	0.002	0.998	0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.002	0.998	0.000
M00.96 Pyogenic arthritis, unspecified (Lower leg)	0.000	0.998	0.002
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
J06.9 Acute upper respiratory infection, unspecified	0.000	0.998	0.002
Q50.4 Embryonic cyst of Fallopian tube	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
Q82.5 Congenital nonneoplastic naevus	0.002	0.998	0.000
N03.9 Unspecified	0.000	0.998	0.002
Q44.6 Cystic disease of liver	0.002	0.998	0.000
Q51.8 Other congenital malformations of uterus and cervix	0.002	0.998	0.000
H19 Disorders of sclera and cornea in diseases classified elsewhere	0.000	0.998	0.002
H17.9 Corneal scar and opacity, unspecified	0.000	0.998	0.002
Q82.9 Congenital malformation of skin, unspecified	0.002	0.998	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.002	0.998	0.000
Q82.3 Incontinentia pigmenti	0.002	0.998	0.000
Q82.2 Mastocytosis	0.002	0.998	0.000
Q82.1 Xeroderma pigmentosum	0.002	0.998	0.000
Q82.0 Hereditary lymphoedema	0.002	0.998	0.000
Q43.3 Congenital malformations of intestinal fixation	0.002	0.998	0.000
I66 Occlusion and stenosis of cerebral arteries, not resulting in cerebral infarction	0.002	0.998	0.000
H16.1 Other superficial keratitis without conjunctivitis	0.000	0.998	0.002
I62 Other nontraumatic intracranial haemorrhage	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.002	0.998	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
Z01.8 Other specified special examinations	0.000	0.998	0.002
H21 Other disorders of iris and ciliary body	0.000	0.998	0.002
I64 Stroke, not specified as haemorrhage or infarction	0.002	0.998	0.000
Q54 Hypospadias	0.002	0.998	0.000
H17.8 Other corneal scars and opacities	0.000	0.998	0.002
H17.1 Other central corneal opacity	0.000	0.998	0.002
H17.0 Adherent leukoma	0.000	0.998	0.002
E21.0 Primary hyperparathyroidism	0.002	0.998	0.000
H16.2 Keratoconjunctivitis	0.000	0.998	0.002
I62.9 Intracranial haemorrhage (nontraumatic), unspecified	0.002	0.998	0.000
I69.3 Sequelae of cerebral infarction	0.002	0.998	0.000
Q43.7 Persistent cloaca	0.002	0.998	0.000
Q43.6 Congenital fistula of rectum and anus	0.002	0.998	0.000
Q43.5 Ectopic anus	0.002	0.998	0.000
Q43.4 Duplication of intestine	0.002	0.998	0.000
Q43.2 Other congenital functional disorders of colon	0.002	0.998	0.000
Q43.1 Hirschsprung's disease	0.002	0.998	0.000
Q54.0 Hypospadias, balanic	0.002	0.998	0.000
Q51 Congenital malformations of uterus and cervix	0.002	0.998	0.000
H15.9 Disorder of sclera, unspecified	0.000	0.998	0.002
H15.8 Other disorders of sclera	0.000	0.998	0.002
H15.1 Episcleritis	0.000	0.998	0.002
H15.0 Scleritis	0.000	0.998	0.002
Q07.9 Congenital malformation of nervous system, unspecified	0.002	0.998	0.000
Q07.8 Other specified congenital malformations of nervous system	0.002	0.998	0.000
Q38.8 Other congenital malformations of pharynx	0.002	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.998	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.002	0.998	0.000
Q38.3 Other congenital malformations of tongue	0.002	0.998	0.000
Q38.2 Macroglossia	0.002	0.998	0.000
Q38.1 Ankyloglossia	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
I68 Cerebrovascular disorders in diseases classified elsewhere	0.002	0.998	0.000
Q89 Other congenital malformations, not elsewhere classified	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
Q53 Undescended testicle	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.002	0.998	0.000
M87.95 Osteonecrosis, unspecified (Pelvic region and thigh)	0.000	0.998	0.002
M10.9 Gout, unspecified	0.000	0.998	0.002
Q56 Indeterminate sex and pseudohermaphroditism	0.002	0.998	0.000
Q55 Other congenital malformations of male genital organs	0.002	0.998	0.000
Q52 Other congenital malformations of female genitalia	0.002	0.998	0.000
R16 Hepatomegaly and splenomegaly, not elsewhere classified	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q44.4 Choledochal cyst	0.002	0.998	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.002	0.998	0.000
Q44.2 Atresia of bile ducts	0.002	0.998	0.000
Q44.1 Other congenital malformations of gallbladder	0.002	0.998	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.002	0.998	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.002	0.998	0.000
Q84 Other congenital malformations of integument	0.002	0.998	0.000
Q81 Epidermolysis bullosa	0.002	0.998	0.000
Q80 Congenital ichthyosis	0.002	0.998	0.000
H22.8 Other disorders of iris and ciliary body in diseases classified elsewhere	0.000	0.998	0.002
H22.0 Iridocyclitis in infectious and parasitic diseases classified elsewhere	0.000	0.998	0.002
H53.9 Visual disturbance, unspecified	0.002	0.998	0.000
O70.0 First degree perineal laceration during delivery	0.000	0.998	0.002
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
I61.5 Intracerebral haemorrhage, intraventricular	0.002	0.998	0.000
I66.9 Occlusion and stenosis of unspecified cerebral artery	0.002	0.998	0.000
F17 Mental and behavioural disorders due to use of tobacco	0.002	0.998	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
M81.4 Drug-induced osteoporosis	0.002	0.998	0.000
Q50.6 Other congenital malformatons of Fallopian tube and broad ligament	0.002	0.998	0.000
Q50.5 Embryonic cyst of broad ligament	0.002	0.998	0.000
Q50.3 Other congenital malformations of ovary	0.002	0.998	0.000
Q50.2 Congenital torsion of ovary	0.002	0.998	0.000
Q50.1 Developmental ovarian cyst	0.002	0.998	0.000
Q50.0 Congenital absence of ovary	0.002	0.998	0.000
I61 Intracerebral haemorrhage	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
I69.1 Sequelae of intracerebral haemorrhage	0.002	0.998	0.000
Q79.6 Ehlers-Danlos syndrome	0.002	0.998	0.000
T17.2 Foreign body in pharynx	0.000	0.998	0.002
Y57.9 Drug or medicament, unspecified	0.002	0.998	0.000
Q83 Congenital malformations of breast	0.002	0.998	0.000
E78.9 Disorder of lipoprotein metabolism, unspecified	0.000	0.998	0.002
F17.1 Harmful use	0.002	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.002	0.998	0.000
Q04 Other congenital malformations of brain	0.002	0.998	0.000
Q03 Congenital hydrocephalus	0.002	0.998	0.000
Q01 Encephalocele	0.002	0.998	0.000
Q00 Anencephaly and similar malformations	0.002	0.998	0.000
Q02 Microcephaly	0.002	0.998	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.002	0.998	0.000
M19.95 Arthrosis, unspecified (Pelvic region and thigh)	0.000	0.998	0.002
H19.8 Other disorders of sclera and cornea in diseases classified elsewhere	0.000	0.998	0.001
H19.2 Keratitis and keratoconjunctivitis in other infectious and parasitic diseases classified elsewhere	0.000	0.998	0.001
H19.0 Scleritis and episcleritis in diseases classified elsewhere	0.000	0.998	0.001
I66.8 Occlusion and stenosis of other cerebral artery	0.002	0.998	0.000
I66.4 Occlusion and stenosis of multiple and bilateral cerebral arteries	0.002	0.998	0.000
I66.3 Occlusion and stenosis of cerebellar arteries	0.002	0.998	0.000
I66.2 Occlusion and stenosis of posterior cerebral artery	0.002	0.998	0.000
I66.1 Occlusion and stenosis of anterior cerebral artery	0.002	0.998	0.000
I66.0 Occlusion and stenosis of middle cerebral artery	0.002	0.998	0.000
Q67.5 Congenital deformity of spine	0.002	0.998	0.000
Q89.2 Congenital malformations of other endocrine glands	0.002	0.998	0.000
H22.1 Iridocyclitis in other diseases classified elsewhere	0.000	0.998	0.001
I62.1 Nontraumatic extradural haemorrhage	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.001	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.001	0.998	0.000
Q40.1 Congenital hiatus hernia	0.001	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.001	0.998	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.001	0.998	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.001	0.998	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.001	0.998	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.001	0.998	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.001	0.998	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.001	0.998	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.001	0.998	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.001	0.998	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.001	0.998	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.001	0.998	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.001	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.001	0.998	0.000
Q45.8 Other specified congenital malformations of digestive system	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
R16.0 Hepatomegaly, not elsewhere classified	0.002	0.998	0.000
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
Q60-Q64 Congenital malformations of the urinary system	0.002	0.998	0.000
G59.0 Diabetic mononeuropathy	0.002	0.998	0.000
H21.9 Disorder of iris and ciliary body, unspecified	0.000	0.998	0.001
H21.4 Pupillary membranes	0.000	0.998	0.001
H21.3 Cyst of iris, ciliary body and anterior chamber	0.000	0.998	0.001
H21.2 Degeneration of iris and ciliary body	0.000	0.998	0.001
H21.1 Other vascular disorders of iris and ciliary body	0.000	0.998	0.001
H21.0 Hyphaema	0.000	0.998	0.001
Q54.8 Other hypospadias	0.001	0.998	0.000
Q54.4 Congenital chordee	0.001	0.998	0.000
Q54.3 Hypospadias, perineal	0.001	0.998	0.000
Q54.2 Hypospadias, penoscrotal	0.001	0.998	0.000
Q54.1 Hypospadias, penile	0.001	0.998	0.000
K40.2 Bilateral inguinal hernia, without obstruction or gangrene	0.002	0.998	0.000
Q51.9 Congenital malformation of uterus and cervix, unspecified	0.001	0.998	0.000
Q51.7 Congenital fistulae between uterus and digestive and urinary tracts	0.001	0.998	0.000
Q51.6 Embryonic cyst of cervix	0.001	0.998	0.000
Q51.5 Agenesis and aplasia of cervix	0.001	0.998	0.000
Q51.4 Unicornate uterus	0.001	0.998	0.000
Q51.2 Other doubling of uterus	0.001	0.998	0.000
Q51.1 Doubling of uterus with doubling of cervix and vagina	0.001	0.998	0.000
Q51.0 Agenesis and aplasia of uterus	0.001	0.998	0.000
I61.0 Intracerebral haemorrhage in hemisphere, subcortical	0.002	0.998	0.000
Q53.1 Undescended testicle, unilateral	0.001	0.998	0.000
Q74.1 Congenital malformation of knee	0.001	0.998	0.000
Q89.9 Congenital malformation, unspecified	0.001	0.998	0.000
Q89.8 Other specified congenital malformations	0.001	0.998	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.001	0.998	0.000
Q89.4 Conjoined twins	0.001	0.998	0.000
Q89.3 Situs inversus	0.001	0.998	0.000
Q89.1 Congenital malformations of adrenal gland	0.001	0.998	0.000
Q89.0 Congenital malformations of spleen	0.001	0.998	0.000
I68.8 Other cerebrovascular disorders in diseases classified elsewhere	0.001	0.998	0.000
I68.2 Cerebral arteritis in other diseases classified elsewhere	0.001	0.998	0.000
I68.1 Cerebral arteritis in infectious and parasitic diseases classified elsewhere	0.001	0.998	0.000
I68.0 Cerebral amyloid angiopathy	0.001	0.998	0.000
Q78 Other osteochondrodysplasias	0.001	0.998	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.001	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.001	0.998	0.000
Q73 Reduction defects of unspecified limb	0.001	0.998	0.000
Q72 Reduction defects of lower limb	0.001	0.998	0.000
Q71 Reduction defects of upper limb	0.001	0.998	0.000
Q70 Syndactyly	0.001	0.998	0.000
Q69 Polydactyly	0.001	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.001	0.998	0.000
H19.3 Keratitis and keratoconjunctivitis in other diseases classified elsewhere	0.000	0.998	0.001
H19.1 Herpesviral keratitis and keratoconjunctivitis	0.000	0.998	0.001
H21.5 Other adhesions and disruptions of iris and ciliary body	0.000	0.998	0.001
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
Q39.6 Diverticulum 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
Q43.0 Meckel's diverticulum	0.001	0.998	0.000
Q53.9 Undescended testicle, unspecified	0.001	0.998	0.000
Q53.2 Undescended testicle, bilateral	0.001	0.998	0.000
Q53.0 Ectopic testis	0.001	0.998	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.001	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.001	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.001	0.998	0.000
Q63.2 Ectopic kidney	0.001	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
M10.98 Gout, unspecified (Other)	0.000	0.998	0.001
M10.95 Gout, unspecified (Pelvic region and thigh)	0.000	0.998	0.001
M10.94 Gout, unspecified (Hand)	0.000	0.998	0.001
M10.92 Gout, unspecified (Upper arm)	0.000	0.998	0.001
M10.91 Gout, unspecified (Shoulder region)	0.000	0.998	0.001
D10.3 Other and unspecified parts of mouth	0.000	0.998	0.002
H81.0 Meniere's disease	0.002	0.998	0.000
Q52.9 Congenital malformation of female genitalia, unspecified	0.001	0.998	0.000
Q52.8 Other specified congenital malformations of female genitalia	0.001	0.998	0.000
Q52.7 Other congenital malformations of vulva	0.001	0.998	0.000
Q52.6 Congenital malformation of clitoris	0.001	0.998	0.000
Q52.5 Fusion of labia	0.001	0.998	0.000
Q52.4 Other congenital malformations of vagina	0.001	0.998	0.000
Q52.3 Imperforate hymen	0.001	0.998	0.000
Q52.2 Congenital rectovaginal fistula	0.001	0.998	0.000
Q52.1 Doubling of vagina	0.001	0.998	0.000
Q52.0 Congenital absence of vagina	0.001	0.998	0.000
Q55.9 Congenital malformation of male genital organ, unspecified	0.001	0.998	0.000
Q55.8 Other specified congenital malformations of male genital organs	0.001	0.998	0.000
Q55.6 Other congenital malformations of penis	0.001	0.998	0.000
Q55.5 Congenital absence and aplasia of penis	0.001	0.998	0.000
Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate	0.001	0.998	0.000
Q55.3 Atresia of vas deferens	0.001	0.998	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.001	0.998	0.000
Q55.1 Hypoplasia of testis and scrotum	0.001	0.998	0.000
Q55.0 Absence and aplasia of testis	0.001	0.998	0.000
Q56.4 Indeterminate sex, unspecified	0.001	0.998	0.000
Q56.3 Pseudohermaphroditism, unspecified	0.001	0.998	0.000
Q56.2 Female pseudohermaphroditism, not elsewhere classified	0.001	0.998	0.000
Q56.1 Male pseudohermaphroditism, not elsewhere classified	0.001	0.998	0.000
Q56.0 Hermaphroditism, not elsewhere classified	0.001	0.998	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.001	0.998	0.000
M19.90 Arthrosis, unspecified (Multiple sites)	0.000	0.998	0.002
M81.49 Drug-induced osteoporosis (Site unspecified)	0.001	0.998	0.000
M84.11 Nonunion of fracture [pseudarthrosis] (Shoulder region)	0.001	0.998	0.000
Q80.9 Congenital ichthyosis, unspecified	0.001	0.998	0.000
Q80.8 Other congenital ichthyosis	0.001	0.998	0.000
Q80.4 Harlequin foetus	0.001	0.998	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.001	0.998	0.000
Q80.2 Lamellar ichthyosis	0.001	0.998	0.000
Q80.1 X-linked ichthyosis	0.001	0.998	0.000
Q80.0 Ichthyosis vulgaris	0.001	0.998	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.001	0.998	0.000
Q81.8 Other epidermolysis bullosa	0.001	0.998	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.001	0.998	0.000
Q81.1 Epidermolysis bullosa letalis	0.001	0.998	0.000
Q81.0 Epidermolysis bullosa simplex	0.001	0.998	0.000
Q84.9 Congenital malformation of integument, unspecified	0.001	0.998	0.000
Q84.8 Other specified congenital malformations of integument	0.001	0.998	0.000
Q84.6 Other congenital malformations of nails	0.001	0.998	0.000
Q84.5 Enlarged and hypertrophic nails	0.001	0.998	0.000
Q84.4 Congenital leukonychia	0.001	0.998	0.000
Q84.3 Anonychia	0.001	0.998	0.000
Q84.2 Other congenital malformations of hair	0.001	0.998	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.001	0.998	0.000
Q84.0 Congenital alopecia	0.001	0.998	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.001	0.998	0.000
Q86.2 Dysmorphism due to warfarin	0.001	0.998	0.000
Q86.1 Foetal hydantoin syndrome	0.001	0.998	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.001	0.998	0.000
F17.9 Unspecified mental and behavioural disorder	0.001	0.998	0.000
F17.8 Other mental and behavioural disorders	0.001	0.998	0.000
F17.7 Residual and late-onset psychotic disorder	0.001	0.998	0.000
F17.6 Amnesic syndrome	0.001	0.998	0.000
F17.5 Psychotic disorder	0.001	0.998	0.000
F17.4 Withdrawal state with delirium	0.001	0.998	0.000
F17.3 Withdrawal state	0.001	0.998	0.000
F17.0 Acute intoxication	0.001	0.998	0.000
N83.8 Other noninflammatory disorders of ovary, Fallopian tube and broad ligament	0.002	0.998	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.001	0.998	0.000
Q79.8 Other congenital malformations of musculoskeletal system	0.001	0.998	0.000
Q79.5 Other congenital malformations of abdominal wall	0.001	0.998	0.000
Q79.4 Prune belly syndrome	0.001	0.998	0.000
Q79.3 Gastroschisis	0.001	0.998	0.000
Q79.2 Exomphalos	0.001	0.998	0.000
Q79.1 Other congenital malformations of diaphragm	0.001	0.998	0.000
Q79.0 Congenital diaphragmatic hernia	0.001	0.998	0.000
M81.48 Drug-induced osteoporosis (Other)	0.001	0.998	0.000
M81.47 Drug-induced osteoporosis (Ankle and foot)	0.001	0.998	0.000
M81.46 Drug-induced osteoporosis (Lower leg)	0.001	0.998	0.000
M81.45 Drug-induced osteoporosis (Pelvic region and thigh)	0.001	0.998	0.000
M81.44 Drug-induced osteoporosis (Hand)	0.001	0.998	0.000
M81.43 Drug-induced osteoporosis (Forearm)	0.001	0.998	0.000
M81.42 Drug-induced osteoporosis (Upper arm)	0.001	0.998	0.000
M81.41 Drug-induced osteoporosis (Shoulder region)	0.001	0.998	0.000
I61.6 Intracerebral haemorrhage, multiple localised	0.001	0.998	0.000
Q67.8 Other congenital deformities of chest	0.001	0.998	0.000
Q67.7 Pectus carinatum	0.001	0.998	0.000
Q67.6 Pectus excavatum	0.001	0.998	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.001	0.998	0.000
Q67.3 Plagiocephaly	0.001	0.998	0.000
Q67.2 Dolichocephaly	0.001	0.998	0.000
Q67.1 Compression facies	0.001	0.998	0.000
Q67.0 Facial asymmetry	0.001	0.998	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.001	0.998	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.001	0.998	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.001	0.998	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.001	0.998	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.001	0.998	0.000
Q05 Spina bifida	0.001	0.998	0.000
S52.00 Fracture of upper end of ulna (closed)	0.000	0.998	0.002
I61.3 Intracerebral haemorrhage in brain stem	0.001	0.998	0.000
N31.8 Other neuromuscular dysfunction of bladder	0.002	0.998	0.000
Q54.9 Hypospadias, unspecified	0.001	0.998	0.000
Q83.9 Congenital malformation of breast, unspecified	0.001	0.998	0.000
Q83.8 Other congenital malformations of breast	0.001	0.998	0.000
Q83.3 Accessory nipple	0.001	0.998	0.000
Q83.2 Absent nipple	0.001	0.998	0.000
Q83.0 Congenital absence of breast with absent nipple	0.001	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.001	0.998	0.000
Q33 Congenital malformations of lung	0.001	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.001	0.998	0.000
Q31 Congenital malformations of larynx	0.001	0.998	0.000
Q30 Congenital malformations of nose	0.001	0.998	0.000
Q37 Cleft palate with cleft lip	0.001	0.998	0.000
Q36 Cleft lip	0.001	0.998	0.000
Q35 Cleft palate	0.001	0.998	0.000
Q66 Congenital deformities of feet	0.001	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.001	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.001	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.001	0.998	0.000
Q96 Turner's syndrome	0.001	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.001	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.001	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.001	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.001	0.998	0.000
Q90 Down's syndrome	0.001	0.998	0.000
M10.97 Gout, unspecified (Ankle and foot)	0.000	0.998	0.001
I60.6 Subarachnoid haemorrhage from other intracranial arteries	0.001	0.998	0.000
Q00.2 Iniencephaly	0.001	0.998	0.000
Q00.1 Craniorachischisis	0.001	0.998	0.000
Q00.0 Anencephaly	0.001	0.998	0.000
Q01.9 Encephalocele, unspecified	0.001	0.998	0.000
Q01.8 Encephalocele of other sites	0.001	0.998	0.000

This table lists the top 500 terms ordered by p(effect).

The full results table can be downloaded from this page.

The TreeWAS Database is the result of research conducted at the Oxford Big Data Institute at the University of Oxford.

This research has been conducted using the UK Biobank Resource (application number 10625). This work uses data provided by patients and collected by the NHS as part of their care and support.

This research has been conducted with the support of the Wellcome Trust (100956/Z/13/Z and 090532/Z/09/Z and 100308/Z/12/Z), the Danish National Research Foundation, Takeda, the Medical Research Council (MC_UU_12010/3), the Oak Foundation (OCAY-15-520), the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC), the Wellcome Trust/Royal Society (204290/Z/16/Z) and the Li Ka Shing Foundation.

Variant-specific associations