TreeWAS – Variant ID: rs6977660

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
K08.8 Other specified disorders of teeth and supporting structures	0.000	0.981	0.019
N13.3 Other and unspecified hydronephrosis	0.011	0.989	0.000
M79.09 Rheumatism, unspecified (Site unspecified)	0.006	0.994	0.000
K82.8 Other specified diseases of gallbladder	0.000	0.994	0.006
N80.0 Endometriosis of uterus	0.006	0.994	0.000
N13.9 Obstructive and reflux uropathy, unspecified	0.005	0.995	0.000
N13 Obstructive and reflux uropathy	0.005	0.995	0.000
N13.0 Hydronephrosis with ureteropelvic junction obstruction	0.005	0.995	0.000
Z86.6 Personal history of diseases of the nervous system and sense organs	0.004	0.996	0.000
N13.5 Kinking and stricture of ureter without hydronephrosis	0.004	0.996	0.000
C18.9 Colon, unspecified	0.004	0.996	0.000
Q63.0 Accessory kidney	0.004	0.996	0.000
N13.8 Other obstructive and reflux uropathy	0.003	0.996	0.000
N13.7 Vesicoureteral-reflux-associated uropathy	0.003	0.996	0.000
C18.3 Hepatic flexure	0.003	0.997	0.000
Z29.1 Prophylactic immunotherapy	0.003	0.997	0.000
Q63 Other congenital malformations of kidney	0.003	0.997	0.000
Z35.2 Supervision of pregnancy with other poor reproductive or obstetric history	0.000	0.997	0.003
C18.4 Transverse colon	0.003	0.997	0.000
L92.9 Granulomatous disorder of skin and subcutaneous tissue, unspecified	0.000	0.997	0.003
N13.2 Hydronephrosis with renal and ureteral calculous obstruction	0.003	0.997	0.000
C18 Malignant neoplasm of colon	0.003	0.997	0.000
N13.4 Hydroureter	0.003	0.997	0.000
L91.8 Other hypertrophic disorders of skin	0.000	0.997	0.003
S20.2 Contusion of thorax	0.003	0.997	0.000
C18.5 Splenic flexure	0.003	0.997	0.000
H43.8 Other disorders of vitreous body	0.000	0.997	0.003
Q63.9 Congenital malformation of kidney, unspecified	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.002	0.998	0.000
Q63.2 Ectopic kidney	0.002	0.998	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.002	0.998	0.000
N13.6 Pyonephrosis	0.002	0.998	0.000
C18.2 Ascending colon	0.002	0.998	0.000
Q62.5 Duplication of ureter	0.002	0.998	0.000
Q60-Q64 Congenital malformations of the urinary system	0.002	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.002	0.998	0.000
C18.8 Overlapping lesion of colon	0.002	0.998	0.000
K08 Other disorders of teeth and supporting structures	0.000	0.998	0.002
M89.97 Disorder of bone, unspecified (Ankle and foot)	0.000	0.998	0.002
Q64 Other congenital malformations of urinary system	0.002	0.998	0.000
C18.1 Appendix	0.002	0.998	0.000
M79.69 Pain in limb (Site unspecified)	0.002	0.998	0.000
M85.89 Other specified disorders of bone density and structure (Site unspecified)	0.002	0.998	0.000
M79.0 Rheumatism, unspecified	0.002	0.998	0.000
C18.7 Sigmoid colon	0.002	0.998	0.000
K56.6 Other and unspecified intestinal obstruction	0.000	0.998	0.002
A08.4 Viral intestinal infection, unspecified	0.000	0.998	0.002
K08.2 Atrophy of edentulous alveolar ridge	0.000	0.998	0.002
N13.1 Hydronephrosis with ureteral stricture, not elsewhere classified	0.002	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.002	0.998	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.002	0.998	0.000
R60.0 Localised oedema	0.000	0.998	0.002
A49.8 Other bacterial infections of unspecified site	0.000	0.998	0.002
D33.3 Cranial nerves	0.000	0.998	0.002
Q62.8 Other congenital malformations of ureter	0.002	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.002	0.998	0.000
Q62.6 Malposition of ureter	0.002	0.998	0.000
Q62.4 Agenesis of ureter	0.002	0.998	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.002	0.998	0.000
Q62.2 Congenital megaloureter	0.002	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.002	0.998	0.000
Q62.0 Congenital hydronephrosis	0.002	0.998	0.000
Q61 Cystic kidney disease	0.002	0.998	0.000
I33.0 Acute and subacute infective endocarditis	0.002	0.998	0.000
R63.0 Anorexia	0.002	0.998	0.000
Z01.7 Laboratory examination	0.002	0.998	0.000
R80 Isolated proteinuria	0.000	0.998	0.002
H43.3 Other vitreous opacities	0.000	0.998	0.002
K08.0 Exfoliation of teeth due to systemic causes	0.000	0.998	0.002
C18.6 Descending colon	0.002	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.002	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.002	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.002	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.002	0.998	0.000
Q64.4 Malformation of urachus	0.002	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.002	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.002	0.998	0.000
Q64.0 Epispadias	0.002	0.998	0.000
Q18.1 Preauricular sinus and cyst	0.002	0.998	0.000
D63.8 Anaemia in other chronic diseases classified elsewhere	0.002	0.998	0.000
N32.3 Diverticulum of bladder	0.002	0.998	0.000
M79.07 Rheumatism, unspecified (Ankle and foot)	0.002	0.998	0.000
M79.06 Rheumatism, unspecified (Lower leg)	0.002	0.998	0.000
M79.05 Rheumatism, unspecified (Pelvic region and thigh)	0.002	0.998	0.000
M79.04 Rheumatism, unspecified (Hand)	0.002	0.998	0.000
M79.03 Rheumatism, unspecified (Forearm)	0.002	0.998	0.000
M79.02 Rheumatism, unspecified (Upper arm)	0.002	0.998	0.000
M79.01 Rheumatism, unspecified (Shoulder region)	0.002	0.998	0.000
M79.08 Rheumatism, unspecified (Other)	0.002	0.998	0.000
H50.2 Vertical strabismus	0.000	0.998	0.002
H50.1 Divergent concomitant strabismus	0.000	0.998	0.002
Q61.9 Cystic kidney disease, unspecified	0.002	0.998	0.000
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
M05.90 Seropositive rheumatoid arthritis, unspecified (Multiple sites)	0.002	0.998	0.000
M25.46 Effusion of joint (Lower leg)	0.000	0.998	0.002
Z29 Need for other prophylactic measures	0.002	0.998	0.000
Q61.8 Other cystic kidney diseases	0.001	0.998	0.000
Q61.4 Renal dysplasia	0.001	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.001	0.998	0.000
S20 Superficial injury of thorax	0.002	0.998	0.000
H52.2 Astigmatism	0.000	0.998	0.002
Q61.5 Medullary cystic kidney	0.001	0.998	0.000
Q61.0 Congenital single renal cyst	0.002	0.998	0.000
H61.0 Perichondritis of external ear	0.002	0.998	0.000
Y88.3 Sequelae of surgical and medical procedures as the cause of abnormal reaction of the patient or of later complication, without mention of misadventure at the time of the procedure	0.002	0.998	0.000
Z29.8 Other specified prophylactic measures	0.002	0.998	0.000
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
J18.1 Lobar pneumonia, unspecified	0.000	0.998	0.002
K07.6 Temporomandibular joint disorders	0.002	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.001	0.998	0.000
L92.0 Granuloma annulare	0.000	0.998	0.001
X41.9 Unspecified place	0.002	0.998	0.000
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency	0.000	0.998	0.002
K08.9 Disorder of teeth and supporting structures, unspecified	0.000	0.998	0.001
Q23.0 Congenital stenosis of aortic valve	0.001	0.998	0.000
H43 Disorders of vitreous body	0.000	0.998	0.002
M84.11 Nonunion of fracture [pseudarthrosis] (Shoulder region)	0.001	0.998	0.000
I84.3 External thrombosed haemorrhoids	0.000	0.998	0.001
N36.0 Urethral fistula	0.000	0.998	0.001
S20.3 Other superficial injuries of front wall of thorax	0.001	0.999	0.000
S20.1 Other and unspecified superficial injuries of breast	0.001	0.999	0.000
Z29.9 Prophylactic measure, unspecified	0.001	0.999	0.000
S20.7 Multiple superficial injuries of thorax	0.001	0.999	0.000
S20.4 Other superficial injuries of back wall of thorax	0.001	0.999	0.000
S20.0 Contusion of breast	0.001	0.999	0.000
Z29.2 Other prophylactic chemotherapy	0.001	0.999	0.000
Q18.0 Sinus, fistula and cyst of branchial cleft	0.001	0.999	0.000
Q61.2 Polycystic kidney, adult type	0.001	0.999	0.000
Q18.9 Congenital malformation of face and neck, unspecified	0.001	0.999	0.000
Q18.8 Other specified congenital malformations of face and neck	0.001	0.999	0.000
Q18.7 Microcheilia	0.001	0.999	0.000
Q18.6 Macrocheilia	0.001	0.999	0.000
Q18.5 Microstomia	0.001	0.999	0.000
Q18.4 Macrostomia	0.001	0.999	0.000
Q18.3 Webbing of neck	0.001	0.999	0.000
Q18.2 Other branchial cleft malformations	0.001	0.999	0.000
X78.0 Home	0.000	0.999	0.001
C79.3 Secondary malignant neoplasm of brain and cerebral meninges	0.000	0.999	0.001
Q24.9 Congenital malformation of the heart, unspecified	0.001	0.999	0.000
M82.10 Osteoporosis in endocrine disorders (Multiple sites)	0.001	0.999	0.000
O42.9 Premature rupture of membranes, unspecified	0.000	0.999	0.001
Q60.6 Potter's syndrome	0.001	0.999	0.000
Q60.5 Renal hypoplasia, unspecified	0.001	0.999	0.000
Q60.4 Renal hypoplasia, bilateral	0.001	0.999	0.000
Q60.3 Renal hypoplasia, unilateral	0.001	0.999	0.000
Q60.1 Renal agenesis, bilateral	0.001	0.999	0.000
L92 Granulomatous disorders of skin and subcutaneous tissue	0.000	0.999	0.001
K12.1 Other forms of stomatitis	0.000	0.999	0.001
Z48.8 Other specified surgical follow-up care	0.001	0.999	0.000
H43.2 Crystalline deposits in vitreous body	0.000	0.999	0.001
H43.0 Vitreous prolapse	0.000	0.999	0.001
R26.0 Ataxic gait	0.001	0.999	0.000
W19.2 School, other institution and public administrative area	0.000	0.999	0.001
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.001	0.999	0.000
C18.0 Caecum	0.001	0.999	0.000
Q24.0 Dextrocardia	0.001	0.999	0.000
N85.0 Endometrial glandular hyperplasia	0.001	0.999	0.000
Q24 Other congenital malformations of heart	0.001	0.999	0.000
M07.39 Other psoriatic arthropathies (Site unspecified)	0.000	0.999	0.001
S27.20 Traumatic haemopneumothorax (without open wound into thoracic cavity)	0.001	0.999	0.000
J18.0 Bronchopneumonia, unspecified	0.000	0.999	0.001
H50 Other strabismus	0.000	0.999	0.001
Q24.5 Malformation of coronary vessels	0.001	0.999	0.000
Q60.2 Renal agenesis, unspecified	0.001	0.999	0.000
S20.8 Superficial injuries of other and unspecified parts of thorax	0.001	0.999	0.000
Z51.4 Preparatory care for treatment, not elsewhere classified	0.000	0.999	0.001
Z92.6 Personal history of chemotherapy for neoplastic disease	0.001	0.999	0.000
Q23 Congenital malformations of aortic and mitral valves	0.001	0.999	0.000
M43.17 Spondylolisthesis (Lumbosacral region)	0.000	0.999	0.001
M60.05 Infective myositis (Pelvic region and thigh)	0.001	0.999	0.000
L92.2 Granuloma faciale [eosinophilic granuloma of skin]	0.000	0.999	0.001
L92.1 Necrobiosis lipoidica, not elsewhere classified	0.000	0.999	0.001
N89.8 Other specified noninflammatory disorders of vagina	0.001	0.999	0.000
H50.9 Strabismus, unspecified	0.000	0.999	0.001
N36.8 Other specified disorders of urethra	0.000	0.999	0.001
S13.4 Sprain and strain of cervical spine	0.001	0.999	0.000
S19.9 Unspecified injury of neck	0.001	0.999	0.000
Z35.9 Supervision of high-risk pregnancy, unspecified	0.000	0.999	0.001
Z35.8 Supervision of other high-risk pregnancies	0.000	0.999	0.001
Q12 Congenital lens malformations	0.001	0.999	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.001	0.999	0.000
A63.0 Anogenital (venereal) warts	0.000	0.999	0.001
H50.4 Other and unspecified heterotropia	0.000	0.999	0.001
I27.2 Other secondary pulmonary hypertension	0.001	0.999	0.000
I62.0 Subdural haemorrhage (acute) (nontraumatic)	0.000	0.999	0.001
Q21.3 Tetralogy of Fallot	0.001	0.999	0.000
Z35.4 Supervision of pregnancy with grand multiparity	0.000	0.999	0.001
Q17 Other congenital malformations of ear	0.001	0.999	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.001	0.999	0.000
Q15 Other congenital malformations of eye	0.001	0.999	0.000
Q14 Congenital malformations of posterior segment of eye	0.001	0.999	0.000
Q13 Congenital malformations of anterior segment of eye	0.001	0.999	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.001	0.999	0.000
M05.94 Seropositive rheumatoid arthritis, unspecified (Hand)	0.001	0.999	0.000
H43.9 Disorder of vitreous body, unspecified	0.000	0.999	0.001
J18.9 Pneumonia, unspecified	0.000	0.999	0.001
Q24.6 Congenital heart block	0.001	0.999	0.000
Q24.4 Congenital subaortic stenosis	0.001	0.999	0.000
Q24.3 Pulmonary infundibular stenosis	0.001	0.999	0.000
Q24.2 Cor triatriatum	0.001	0.999	0.000
Q24.1 Levocardia	0.001	0.999	0.000
T17.5 Foreign body in bronchus	0.001	0.999	0.000
L91 Hypertrophic disorders of skin	0.000	0.999	0.001
Z35 Supervision of high-risk pregnancy	0.000	0.999	0.001
H50.8 Other specified strabismus	0.000	0.999	0.001
H50.6 Mechanical strabismus	0.000	0.999	0.001
H50.3 Intermittent heterotropia	0.000	0.999	0.001
H61.9 Disorder of external ear, unspecified	0.001	0.999	0.000
Z48.0 Attention to surgical dressings and sutures	0.001	0.999	0.000
M79.10 Myalgia (Multiple sites)	0.001	0.999	0.000
D32.0 Cerebral meninges	0.001	0.999	0.000
E06.3 Autoimmune thyroiditis	0.001	0.999	0.000
L92.8 Other granulomatous disorders of skin and subcutaneous tissue	0.000	0.999	0.001
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.001	0.999	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.001	0.999	0.000
Q23.4 Hypoplastic left heart syndrome	0.001	0.999	0.000
Q23.3 Congenital mitral insufficiency	0.001	0.999	0.000
Q23.2 Congenital mitral stenosis	0.001	0.999	0.000
J18 Pneumonia, organism unspecified	0.000	0.999	0.001
Q20-Q28 Congenital malformations of the circulatory system	0.001	0.999	0.000
H61.1 Non-infective disorders of pinna	0.001	0.999	0.000
K08.1 Loss of teeth due to accident, extraction or local periodontal disease	0.000	0.999	0.001
Q10.7 Congenital malformation of orbit	0.001	0.999	0.000
Q10.6 Other congenital malformations of lachrymal apparatus	0.001	0.999	0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct	0.001	0.999	0.000
Q10.4 Absence and agenesis of lachrymal apparatus	0.001	0.999	0.000
Q10.3 Other congenital malformations of eyelid	0.001	0.999	0.000
Q10.2 Congenital entropion	0.001	0.999	0.000
Q10.1 Congenital ectropion	0.001	0.999	0.000
Q10.0 Congenital ptosis	0.001	0.999	0.000
Q12.9 Congenital lens malformation, unspecified	0.001	0.999	0.000
Q12.8 Other congenital lens malformations	0.001	0.999	0.000
Q12.4 Spherophakia	0.001	0.999	0.000
Q12.3 Congenital aphakia	0.001	0.999	0.000
Q12.2 Coloboma of lens	0.001	0.999	0.000
Q12.1 Congenital displaced lens	0.001	0.999	0.000
Y40.0 Penicillins	0.000	0.999	0.001
M62.88 Other specified disorders of muscle (Other)	0.001	0.999	0.000
M87.20 Osteonecrosis due to previous trauma (Multiple sites)	0.001	0.999	0.000
I33.9 Acute endocarditis, unspecified	0.001	0.999	0.000
O43.1 Malformation of placenta	0.000	0.999	0.001
Q11.3 Macrophthalmos	0.001	0.999	0.000
Q11.2 Microphthalmos	0.001	0.999	0.000
Q11.1 Other anophthalmos	0.001	0.999	0.000
Q11.0 Cystic eyeball	0.001	0.999	0.000
Q12.0 Congenital cataract	0.001	0.999	0.000
Q13.9 Congenital malformation of anterior segment of eye, unspecified	0.001	0.999	0.000
Q13.8 Other congenital malformations of anterior segment of eye	0.001	0.999	0.000
Q13.5 Blue sclera	0.001	0.999	0.000
Q13.4 Other congenital corneal malformations	0.001	0.999	0.000
Q13.3 Congenital corneal opacity	0.001	0.999	0.000
Q13.2 Other congenital malformations of iris	0.001	0.999	0.000
Q13.1 Absence of iris	0.001	0.999	0.000
Q13.0 Coloboma of iris	0.001	0.999	0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.001	0.999	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.001	0.999	0.000
Q14.3 Congenital malformation of choroid	0.001	0.999	0.000
Q14.2 Congenital malformation of optic disk	0.001	0.999	0.000
Q14.1 Congenital malformation of retina	0.001	0.999	0.000
Q14.0 Congenital malformation of vitreous humour	0.001	0.999	0.000
Q15.9 Congenital malformation of eye, unspecified	0.001	0.999	0.000
Q15.8 Other specified congenital malformations of eye	0.001	0.999	0.000
Q15.0 Congenital glaucoma	0.001	0.999	0.000
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified	0.001	0.999	0.000
Q16.5 Congenital malformation of inner ear	0.001	0.999	0.000
Q16.4 Other congenital malformations of middle ear	0.001	0.999	0.000
Q16.3 Congenital malformation of ear ossicles	0.001	0.999	0.000
Q16.2 Absence of eustachian tube	0.001	0.999	0.000
Q16.1 Congenital absence, atresia and stricture of auditory canal (external)	0.001	0.999	0.000
Q16.0 Congenital absence of (ear) auricle	0.001	0.999	0.000
Q17.9 Congenital malformation of ear, unspecified	0.001	0.999	0.000
Q17.8 Other specified congenital malformations of ear	0.001	0.999	0.000
Q17.5 Prominent ear	0.001	0.999	0.000
Q17.4 Misplaced ear	0.001	0.999	0.000
Q17.3 Other misshapen ear	0.001	0.999	0.000
Q17.2 Microtia	0.001	0.999	0.000
Q17.1 Macrotia	0.001	0.999	0.000
Q17.0 Accessory auricle	0.001	0.999	0.000
Q90.9 Down's syndrome, unspecified	0.001	0.999	0.000
Z00.0 General medical examination	0.001	0.999	0.000
Q25 Congenital malformations of great arteries	0.001	0.999	0.000
M79.25 Neuralgia and neuritis, unspecified (Pelvic region and thigh)	0.001	0.999	0.000
M85.88 Other specified disorders of bone density and structure (Other)	0.001	0.999	0.000
A87.9 Viral meningitis, unspecified	0.000	0.999	0.001
F33.8 Other recurrent depressive disorders	0.001	0.999	0.000
L91.9 Hypertrophic disorder of skin, unspecified	0.000	0.999	0.001
M85.8 Other specified disorders of bone density and structure	0.001	0.999	0.000
Q25.0 Patent ductus arteriosus	0.001	0.999	0.000
Q38.7 Pharyngeal pouch	0.000	0.999	0.001
Z35.7 Supervision of high-risk pregnancy due to social problems	0.000	0.999	0.001
Z35.6 Supervision of very young primigravida	0.000	0.999	0.001
Z35.3 Supervision of pregnancy with history of insufficient antenatal care	0.000	0.999	0.001
Q90 Down's syndrome	0.001	0.999	0.000
M79.00 Rheumatism, unspecified (Multiple sites)	0.001	0.999	0.000
J18.8 Other pneumonia, organism unspecified	0.000	0.999	0.001
J18.2 Hypostatic pneumonia, unspecified	0.000	0.999	0.001
Q60.0 Renal agenesis, unilateral	0.001	0.999	0.000
S27.2 Traumatic heamopneumothorax	0.001	0.999	0.000
Q26 Congenital malformations of great veins	0.001	0.999	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.001	0.999	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.001	0.999	0.000
X41 Accidental poisoning by and exposure to antiepileptic, sedative-hypnotic, anti-Parkinsonism and psychotropic drugs, not elsewhere classified	0.001	0.999	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.001	0.999	0.000
M89.94 Disorder of bone, unspecified (Hand)	0.000	0.999	0.001
F33.9 Recurrent depressive disorder, unspecified	0.001	0.999	0.000
M05.9 Seropositive rheumatoid arthritis, unspecified	0.001	0.999	0.000
O43.8 Other placental disorders	0.000	0.999	0.001
Q25.9 Congenital malformation of great arteries, unspecified	0.001	0.999	0.000
Q25.8 Other congenital malformations of great arteries	0.001	0.999	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.001	0.999	0.000
Q25.6 Stenosis of pulmonary artery	0.001	0.999	0.000
Q25.5 Atresia of pulmonary artery	0.001	0.999	0.000
Q25.4 Other congenital malformations of aorta	0.001	0.999	0.000
Q25.3 Stenosis of aorta	0.001	0.999	0.000
Q25.2 Atresia of aorta	0.001	0.999	0.000
Q25.1 Coarctation of aorta	0.001	0.999	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.001	0.999	0.000
W20.0 Home	0.000	0.999	0.001
Z29.0 Isolation	0.001	0.999	0.000
M71.26 Synovial cyst of popliteal space [Baker]-Lower Leg	0.000	0.999	0.001
M85.87 Other specified disorders of bone density and structure (Ankle and foot)	0.001	0.999	0.000
M85.86 Other specified disorders of bone density and structure (Lower leg)	0.001	0.999	0.000
M85.84 Other specified disorders of bone density and structure (Hand)	0.001	0.999	0.000
M85.83 Other specified disorders of bone density and structure (Forearm)	0.001	0.999	0.000
M85.82 Other specified disorders of bone density and structure (Upper arm)	0.001	0.999	0.000
M85.81 Other specified disorders of bone density and structure (Shoulder region)	0.001	0.999	0.000
B17.1 Acute hepatitis C	0.000	0.999	0.001
H50.5 Heterophoria	0.000	0.999	0.001
L23.1 Allergic contact dermatitis due to adhesives	0.001	0.999	0.000
M89.9 Disorder of bone, unspecified	0.000	0.999	0.001
Q83.8 Other congenital malformations of breast	0.001	0.999	0.000
Q90.2 Trisomy 21, translocation	0.001	0.999	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.001	0.999	0.000
S46.2 Injury of muscle and tendon of other parts of biceps	0.000	0.999	0.001
Q96 Turner's syndrome	0.001	0.999	0.000
M79.46 Hypertrophy of (infrapatellar) fat pad (Lower leg)	0.001	0.999	0.000
S12.70 Multiple fractures of cervical spine (closed)	0.001	0.999	0.000
S27.10 Traumatic haemothorax (without open wound into thoracic cavity)	0.001	0.999	0.000
S27.21 Traumatic haemopneumothorax (with open wound into thoracic cavity)	0.001	0.999	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.001	0.999	0.000
M82.1 Osteoporosis in endocrine disorders	0.001	0.999	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.001	0.999	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.001	0.999	0.000
Q20.6 Isomerism of atrial appendages	0.001	0.999	0.000
Q20.5 Discordant atrioventricular connexion	0.001	0.999	0.000
Q20.4 Double inlet ventricle	0.001	0.999	0.000
Q20.3 Discordant ventriculoarterial connexion	0.001	0.999	0.000
Q20.2 Double outlet left ventricle	0.001	0.999	0.000
Q20.1 Double outlet right ventricle	0.001	0.999	0.000
Q20.0 Common arterial trunk	0.001	0.999	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.001	0.999	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.001	0.999	0.000
Q22.6 Hypoplastic right heart syndrome	0.001	0.999	0.000
Q22.5 Ebstein's anomaly	0.001	0.999	0.000
Q22.4 Congenital tricuspid stenosis	0.001	0.999	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.001	0.999	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.001	0.999	0.000
Q22.1 Congenital pulmonary valve stenosis	0.001	0.999	0.000
Q22.0 Pulmonary valve atresia	0.001	0.999	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.001	0.999	0.000
Q26.8 Other congenital malformations of great veins	0.001	0.999	0.000
Q26.6 Portal vein-hepatic artery fistula	0.001	0.999	0.000
Q26.5 Anomalous portal venous connexion	0.001	0.999	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.001	0.999	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.001	0.999	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.001	0.999	0.000
Q26.1 Persistent left superior vena cava	0.001	0.999	0.000
Q26.0 Congenital stenosis of vena cava	0.001	0.999	0.000
Q96.9 Turner's syndrome, unspecified	0.001	0.999	0.000
S11.8 Open wound of other parts of neck	0.001	0.999	0.000
T93.8 Sequelae of other specified injuries of lower limb	0.000	0.999	0.001
X41.0 Home	0.001	0.999	0.000
X41.8 Other specified place	0.001	0.999	0.000
X41.7 Farm	0.001	0.999	0.000
X41.6 Industrial and construction area	0.001	0.999	0.000
X41.5 Trade and service area	0.001	0.999	0.000
X41.4 Street and highway	0.001	0.999	0.000
X41.3 Sports and athletics area	0.001	0.999	0.000
X41.2 School, other institution and public administrative area	0.001	0.999	0.000
X41.1 Residential institution	0.001	0.999	0.000
Z82.3 Family history of stroke	0.000	0.999	0.001
Q21 Congenital malformations of cardiac septa	0.001	0.999	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.001	0.999	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.001	0.999	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.001	0.999	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.001	0.999	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.001	0.999	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.001	0.999	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.001	0.999	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.001	0.999	0.000
M05.98 Seropositive rheumatoid arthritis, unspecified (Other)	0.001	0.999	0.000
M05.96 Seropositive rheumatoid arthritis, unspecified (Lower leg)	0.001	0.999	0.000
M05.95 Seropositive rheumatoid arthritis, unspecified (Pelvic region and thigh)	0.001	0.999	0.000
M05.93 Seropositive rheumatoid arthritis, unspecified (Forearm)	0.001	0.999	0.000
M05.92 Seropositive rheumatoid arthritis, unspecified (Upper arm)	0.001	0.999	0.000
M05.91 Seropositive rheumatoid arthritis, unspecified (Shoulder region)	0.001	0.999	0.000
M07.36 Other psoriatic arthropathies (Lower leg)	0.000	0.999	0.001
I62.9 Intracranial haemorrhage (nontraumatic), unspecified	0.000	0.999	0.001
N36.3 Prolapsed urethral mucosa	0.000	0.999	0.001
Q24.8 Other specified congenital malformations of heart	0.001	0.999	0.000
Q96.8 Other variants of Turner's syndrome	0.001	0.999	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.001	0.999	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.001	0.999	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.001	0.999	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.001	0.999	0.000
Q96.0 Karyotype 45,X	0.001	0.999	0.000
B91 Sequelae of poliomyelitis	0.000	0.999	0.001
S19 Other and unspecified injuries of neck	0.001	0.999	0.000
M07.30 Other psoriatic arthropathies (Multiple sites)	0.000	0.999	0.001
M82.19 Osteoporosis in endocrine disorders (Site unspecified)	0.001	0.999	0.000
M82.18 Osteoporosis in endocrine disorders (Other)	0.001	0.999	0.000
M82.17 Osteoporosis in endocrine disorders (Ankle and foot)	0.001	0.999	0.000
M82.16 Osteoporosis in endocrine disorders (Lower leg)	0.001	0.999	0.000
M82.15 Osteoporosis in endocrine disorders (Pelvic region and thigh)	0.001	0.999	0.000
M82.14 Osteoporosis in endocrine disorders (Hand)	0.001	0.999	0.000
M82.13 Osteoporosis in endocrine disorders (Forearm)	0.001	0.999	0.000
M82.12 Osteoporosis in endocrine disorders (Upper arm)	0.001	0.999	0.000
M82.11 Osteoporosis in endocrine disorders (Shoulder region)	0.001	0.999	0.000
M87.25 Osteonecrosis due to previous trauma (Pelvic region and thigh)	0.001	0.999	0.000
M89.99 Disorder of bone, unspecified (Site unspecified)	0.000	0.999	0.001
M89.93 Disorder of bone, unspecified (Forearm)	0.000	0.999	0.001
M89.92 Disorder of bone, unspecified (Upper arm)	0.000	0.999	0.001
M89.91 Disorder of bone, unspecified (Shoulder region)	0.000	0.999	0.001
M89.90 Disorder of bone, unspecified (Multiple sites)	0.000	0.999	0.001
X41.08 Accidental poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified , Home ,While engaged in other specified activities	0.001	0.999	0.000
C49.2 Connective and soft tissue of lower limb, including hip	0.000	0.999	0.001
L23.9 Allergic contact dermatitis, unspecified cause	0.001	0.999	0.000
L91.0 Keloid scar	0.000	0.999	0.001
Q21.9 Congenital malformation of cardiac septum, unspecified	0.001	0.999	0.000
Q21.8 Other congenital malformations of cardiac septa	0.001	0.999	0.000
Q21.4 Aortopulmonary septal defect	0.001	0.999	0.000
Q21.2 Atrioventricular septal defect	0.001	0.999	0.000
Q21.0 Ventricular septal defect	0.001	0.999	0.000
Q43.0 Meckel's diverticulum	0.001	0.999	0.000
Q91.7 Patau's syndrome, unspecified	0.001	0.999	0.000
Q91.6 Trisomy 13, translocation	0.001	0.999	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.001	0.999	0.000
Q91.3 Edwards' syndrome, unspecified	0.001	0.999	0.000
Q91.2 Trisomy 18, translocation	0.001	0.999	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.001	0.999	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.001	0.999	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.001	0.999	0.000
Q92.7 Triploidy and polyploidy	0.001	0.999	0.000
Q92.6 Extra marker chromosomes	0.001	0.999	0.000
Q92.5 Duplications with other complex rearrangements	0.001	0.999	0.000
Q92.4 Duplications seen only at prometaphase	0.001	0.999	0.000
Q92.3 Minor partial trisomy	0.001	0.999	0.000
Q92.2 Major partial trisomy	0.001	0.999	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.001	0.999	0.000
Q93.9 Deletion from autosomes, unspecified	0.001	0.999	0.000
Q93.8 Other deletions from the autosomes	0.001	0.999	0.000
Q93.7 Deletions with other complex rearrangements	0.001	0.999	0.000
Q93.6 Deletions seen only at prometaphase	0.001	0.999	0.000
Q93.5 Other deletions of part of a chromosome	0.001	0.999	0.000
Q93.4 Deletion of short arm of chromosome 5	0.001	0.999	0.000
Q93.3 Deletion of short arm of chromosome 4	0.001	0.999	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.001	0.999	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.001	0.999	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.001	0.999	0.000
Q95.8 Other balanced rearrangements and structural markers	0.001	0.999	0.000
Q95.5 Individuals with autosomal fragile site	0.001	0.999	0.000
Q95.4 Individuals with marker heterochromatin	0.001	0.999	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.001	0.999	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.001	0.999	0.000
Q95.1 Chromosome inversion in normal individual	0.001	0.999	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.001	0.999	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.001	0.999	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.001	0.999	0.000
Q97.3 Female with 46,XY karyotype	0.001	0.999	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.001	0.999	0.000
Q97.1 Female with more than three X chromosomes	0.001	0.999	0.000
Q97.0 Karyotype 47,XXX	0.001	0.999	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.001	0.999	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.001	0.999	0.000
Q98.7 Male with sex chromosome mosaicism	0.001	0.999	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.001	0.999	0.000
Q98.5 Karyotype 47,XYY	0.001	0.999	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.001	0.999	0.000
Q98.3 Other male with 46,XX karyotype	0.001	0.999	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.001	0.999	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.001	0.999	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.001	0.999	0.000
Q99.9 Chromosomal abnormality, unspecified	0.001	0.999	0.000
Q99.8 Other specified chromosome abnormalities	0.001	0.999	0.000
Q99.2 Fragile X chromosome	0.001	0.999	0.000
Q99.1 46,XX true hermaphrodite	0.001	0.999	0.000
Q99.0 Chimera 46,XX/46,XY	0.001	0.999	0.000
S11.9 Open wound of neck, part unspecified	0.001	0.999	0.000
S19.8 Other specified injuries of neck	0.001	0.999	0.000
Q35-Q37 Cleft lip and cleft palate	0.001	0.999	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.001	0.999	0.000
D41.0 Kidney	0.001	0.999	0.000
F31.9 Bipolar affective disorder, unspecified	0.000	0.999	0.001
K62.7 Radiation proctitis	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