TreeWAS – Variant ID: rs2369304

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
F05.9 Delirium, unspecified	0.000	0.991	0.009
S62.61 Fracture of other finger (open)	0.000	0.993	0.007
N87.9 Dysplasia of cervix uteri, unspecified	0.005	0.995	0.000
F05 Delirium, not induced by alcohol and other psychoactive substances	0.000	0.995	0.005
M47.90 Spondylosis, unspecified (Multiple sites in spine)	0.000	0.996	0.004
F05.1 Delirium superimposed on dementia	0.000	0.996	0.004
F43.2 Adjustment disorders	0.004	0.996	0.000
Q63.0 Accessory kidney	0.004	0.996	0.000
F05.8 Other delirium	0.000	0.996	0.004
F05.0 Delirium not superimposed on dementia, so described	0.000	0.996	0.004
R45.8 Other symptoms and signs involving emotional state	0.004	0.996	0.000
Z48.9 Surgical follow-up care, unspecified	0.000	0.996	0.004
C48.2 Peritoneum, unspecified	0.000	0.997	0.003
B34.8 Other viral infections of unspecified site	0.000	0.997	0.003
Q54 Hypospadias	0.003	0.997	0.000
Q63 Other congenital malformations of kidney	0.003	0.997	0.000
S62.50 Fracture of thumb (closed)	0.000	0.997	0.003
Q50-Q56 Congenital malformations of genital organs	0.003	0.997	0.000
D04.7 Skin of lower limb, including hip	0.003	0.997	0.000
Q54.8 Other hypospadias	0.003	0.997	0.000
Q54.1 Hypospadias, penile	0.003	0.997	0.000
K80.4 Calculus of bile duct with cholecystitis	0.003	0.997	0.000
M10.99 Gout, unspecified (Site unspecified)	0.003	0.997	0.000
Q52 Other congenital malformations of female genitalia	0.003	0.997	0.000
N76.2 Acute vulvitis	0.003	0.997	0.000
Q54.0 Hypospadias, balanic	0.003	0.997	0.000
L03.8 Cellulitis of other sites	0.000	0.997	0.003
Q54.9 Hypospadias, unspecified	0.003	0.997	0.000
H92.1 Otorrhoea	0.000	0.997	0.003
N81.8 Other female genital prolapse	0.003	0.997	0.000
D47.1 Chronic myeloproliferative disease	0.000	0.997	0.003
F43.0 Acute stress reaction	0.002	0.997	0.000
Q53 Undescended testicle	0.002	0.997	0.000
M94.88 Other specified disorders of cartilage (Other)	0.000	0.998	0.002
Q54.4 Congenital chordee	0.002	0.998	0.000
Q54.3 Hypospadias, perineal	0.002	0.998	0.000
Q54.2 Hypospadias, penoscrotal	0.002	0.998	0.000
M10.9 Gout, unspecified	0.002	0.998	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.002	0.998	0.000
Q87.4 Marfan's syndrome	0.002	0.998	0.000
Q52.4 Other congenital malformations of vagina	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.002	0.998	0.000
F43 Reaction to severe stress, and adjustment disorders	0.002	0.998	0.000
Q55 Other congenital malformations of male genital organs	0.002	0.998	0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.002	0.998	0.000
Q63.2 Ectopic kidney	0.002	0.998	0.000
Q52.5 Fusion of labia	0.002	0.998	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.002	0.998	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.002	0.998	0.000
M54.58 Low back pain (Sacral and sacrococcygeal region)	0.002	0.998	0.000
M10.97 Gout, unspecified (Ankle and foot)	0.002	0.998	0.000
E87.7 Fluid overload	0.002	0.998	0.000
R09.8 Other specified symptoms and signs involving the circulatory and respiratory systems	0.000	0.998	0.002
T45.5 Anticoagulants	0.002	0.998	0.000
Q51 Congenital malformations of uterus and cervix	0.002	0.998	0.000
Q07.0 Arnold-Chiari syndrome	0.002	0.998	0.000
Q50.4 Embryonic cyst of Fallopian tube	0.002	0.998	0.000
M10.93 Gout, unspecified (Forearm)	0.002	0.998	0.000
Q53.2 Undescended testicle, bilateral	0.002	0.998	0.000
Q24 Other congenital malformations of heart	0.002	0.998	0.000
S82.20 Fracture of shaft of tibia (closed)	0.000	0.998	0.002
Q24.5 Malformation of coronary vessels	0.002	0.998	0.000
Q52.9 Congenital malformation of female genitalia, unspecified	0.002	0.998	0.000
Q52.8 Other specified congenital malformations of female genitalia	0.002	0.998	0.000
Q52.7 Other congenital malformations of vulva	0.002	0.998	0.000
Q52.6 Congenital malformation of clitoris	0.002	0.998	0.000
Q52.3 Imperforate hymen	0.002	0.998	0.000
Q52.2 Congenital rectovaginal fistula	0.002	0.998	0.000
Q52.0 Congenital absence of vagina	0.002	0.998	0.000
Q24.4 Congenital subaortic stenosis	0.002	0.998	0.000
Q52.1 Doubling of vagina	0.002	0.998	0.000
M94.8 Other specified disorders of cartilage	0.000	0.998	0.002
Q60-Q64 Congenital malformations of the urinary system	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
W10.8 Other specified place	0.000	0.998	0.002
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
M88.90 Paget's disease of bone, unspecified (Multiple sites)	0.000	0.998	0.002
H05.0 Acute inflammation of orbit	0.002	0.998	0.000
C48 Malignant neoplasm of retroperitoneum and peritoneum	0.000	0.998	0.002
Q25.6 Stenosis of pulmonary artery	0.002	0.998	0.000
Q53.9 Undescended testicle, unspecified	0.002	0.998	0.000
M10.94 Gout, unspecified (Hand)	0.002	0.998	0.000
Q53.0 Ectopic testis	0.002	0.998	0.000
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
R03.1 Nonspecific low blood-pressure reading	0.002	0.998	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.002	0.998	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.002	0.998	0.000
Q25 Congenital malformations of great arteries	0.002	0.998	0.000
M10.98 Gout, unspecified (Other)	0.002	0.998	0.000
M10.95 Gout, unspecified (Pelvic region and thigh)	0.002	0.998	0.000
M10.91 Gout, unspecified (Shoulder region)	0.002	0.998	0.000
M10.90 Gout, unspecified (Multiple sites)	0.002	0.998	0.000
Q53.1 Undescended testicle, unilateral	0.002	0.998	0.000
Q51.8 Other congenital malformations of uterus and cervix	0.002	0.998	0.000
Q07.8 Other specified congenital malformations of nervous system	0.002	0.998	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.002	0.998	0.000
M94.26 Chondromalacia (Lower leg)	0.000	0.998	0.002
M94.86 Other specified disorders of cartilage (Lower leg)	0.000	0.998	0.002
F43.8 Other reactions to severe stress	0.002	0.998	0.000
Q50.6 Other congenital malformatons of Fallopian tube and 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
Q55.9 Congenital malformation of male genital organ, unspecified	0.002	0.998	0.000
Q55.8 Other specified congenital malformations of male genital organs	0.002	0.998	0.000
Q55.5 Congenital absence and aplasia of penis	0.002	0.998	0.000
Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate	0.002	0.998	0.000
Q55.3 Atresia of vas deferens	0.002	0.998	0.000
Q55.1 Hypoplasia of testis and scrotum	0.002	0.998	0.000
Q55.0 Absence and aplasia of testis	0.002	0.998	0.000
M65.91 Synovitis and tenosynovitis, unspecified (Shoulder region)	0.000	0.998	0.002
M94.85 Other specified disorders of cartilage (Pelvic region and thigh)	0.000	0.998	0.002
Q55.6 Other congenital malformations of penis	0.002	0.998	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms	0.000	0.998	0.002
Q56.4 Indeterminate sex, unspecified	0.002	0.998	0.000
Q56.3 Pseudohermaphroditism, unspecified	0.002	0.998	0.000
Q56.2 Female pseudohermaphroditism, not elsewhere classified	0.002	0.998	0.000
Q56.1 Male pseudohermaphroditism, not elsewhere classified	0.002	0.998	0.000
Q56.0 Hermaphroditism, not elsewhere classified	0.002	0.998	0.000
M10.96 Gout, unspecified (Lower leg)	0.002	0.998	0.000
N94.9 Unspecified condition associated with female genital organs and menstrual cycle	0.000	0.998	0.002
Q28.2 Arteriovenous malformation of cerebral vessels	0.002	0.998	0.000
Q51.4 Unicornate uterus	0.002	0.998	0.000
C48.0 Retroperitoneum	0.000	0.998	0.002
Q24.8 Other specified congenital malformations of heart	0.002	0.998	0.000
Q51.9 Congenital malformation of uterus and cervix, unspecified	0.002	0.998	0.000
Q51.7 Congenital fistulae between uterus and digestive and urinary tracts	0.002	0.998	0.000
Q51.6 Embryonic cyst of cervix	0.002	0.998	0.000
Q51.5 Agenesis and aplasia of cervix	0.002	0.998	0.000
Q51.1 Doubling of uterus with doubling of cervix and vagina	0.002	0.998	0.000
Q51.0 Agenesis and aplasia of uterus	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
M10.92 Gout, unspecified (Upper arm)	0.002	0.998	0.000
S62.6 Fracture of other finger	0.000	0.998	0.002
X51.9 Unspecified place	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
Q24.6 Congenital heart block	0.002	0.998	0.000
Q24.3 Pulmonary infundibular stenosis	0.002	0.998	0.000
Q24.2 Cor triatriatum	0.002	0.998	0.000
Q24.1 Levocardia	0.002	0.998	0.000
T47.1 Other antacids and anti-gastric-secretion drugs	0.002	0.998	0.000
M94.89 Other specified disorders of cartilage (Site unspecified)	0.000	0.998	0.002
M94.87 Other specified disorders of cartilage (Ankle and foot)	0.000	0.998	0.002
M94.84 Other specified disorders of cartilage (Hand)	0.000	0.998	0.002
M94.83 Other specified disorders of cartilage (Forearm)	0.000	0.998	0.002
M94.82 Other specified disorders of cartilage (Upper arm)	0.000	0.998	0.002
M94.81 Other specified disorders of cartilage (Shoulder region)	0.000	0.998	0.002
M94.80 Other specified disorders of cartilage (Multiple sites)	0.000	0.998	0.002
Q25.4 Other congenital malformations of aorta	0.002	0.998	0.000
D47.3 Essential (haemorrhagic) thrombocythaemia	0.000	0.998	0.002
J38.0 Paralysis of vocal cords and larynx	0.000	0.998	0.002
Q07.9 Congenital malformation of nervous system, unspecified	0.002	0.998	0.000
Q24.0 Dextrocardia	0.002	0.998	0.000
Q51.2 Other doubling of uterus	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.002	0.998	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.002	0.998	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.002	0.998	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.002	0.998	0.000
T45.2 Vitamins, not elsewhere classified	0.002	0.998	0.000
D47 Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue	0.000	0.998	0.002
C48.8 Overlapping lesion of retroperitoneum and peritoneum	0.000	0.998	0.002
N76.1 Subacute and chronic vaginitis	0.002	0.998	0.000
T39.8 Other nonopioid analgesics and antipyretics, not elsewhere classified	0.002	0.998	0.000
W55.0 Home	0.002	0.998	0.000
B34 Viral infection of unspecified site	0.000	0.998	0.002
T45 Poisoning by primarily systemic and haematological agents, not elsewhere classified	0.002	0.998	0.000
S82.21 Fracture of shaft of tibia (open)	0.000	0.998	0.002
A49.8 Other bacterial infections of unspecified site	0.002	0.998	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.002	0.998	0.000
Q64 Other congenital malformations of urinary system	0.002	0.998	0.000
C48.1 Specified parts of peritoneum	0.000	0.998	0.002
K86.1 Other chronic pancreatitis	0.000	0.998	0.002
Q50.5 Embryonic cyst of broad ligament	0.002	0.998	0.000
U80.8 Agent resistant to other penicillin-related antibiotic	0.000	0.998	0.002
U80.1 Methicillin resistant agent	0.000	0.998	0.002
Q99 Other chromosome abnormalities, not elsewhere classified	0.002	0.998	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.002	0.998	0.000
Q25.8 Other congenital malformations of great arteries	0.002	0.998	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.998	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.998	0.000
Q25.2 Atresia of aorta	0.002	0.998	0.000
S64.2 Injury of radial nerve at wrist and hand level	0.000	0.998	0.002
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
M10.39 Gout due to impairment of renal function (Site unspecified)	0.002	0.998	0.000
F43.9 Reaction to severe stress, unspecified	0.002	0.998	0.000
M94.2 Chondromalacia	0.000	0.998	0.002
Q24.9 Congenital malformation of the heart, unspecified	0.002	0.998	0.000
Q25.1 Coarctation of aorta	0.002	0.998	0.000
Q25.0 Patent ductus arteriosus	0.002	0.998	0.000
D34 Benign neoplasm of thyroid gland	0.000	0.998	0.002
M87.95 Osteonecrosis, unspecified (Pelvic region and thigh)	0.000	0.998	0.002
B34.4 Papovirus infection, unspecified	0.000	0.998	0.002
Q25.3 Stenosis of aorta	0.002	0.998	0.000
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
I21.4 Acute subendocardial myocardial infarction	0.000	0.998	0.002
Q22 Congenital malformations of pulmonary and tricuspid valves	0.002	0.998	0.000
F43.1 Posttraumatic stress disorder	0.002	0.998	0.000
M10.3 Gout due to impairment of renal function	0.002	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.002	0.998	0.000
T45.1 Antineoplastic and immunosuppressive drugs	0.002	0.998	0.000
Q61 Cystic kidney disease	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
D47.4 Osteomyelofibrosis	0.000	0.998	0.002
N76.5 Ulceration of vagina	0.002	0.998	0.000
N76 Other inflammation of vagina and vulva	0.002	0.998	0.000
U80 Agent resistant to penicillin and related antibiotics	0.000	0.998	0.002
M10 Gout	0.002	0.998	0.000
Q96 Turner's syndrome	0.002	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.001	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.001	0.998	0.000
Q01 Encephalocele	0.001	0.998	0.000
Q00 Anencephaly and similar malformations	0.001	0.998	0.000
Q02 Microcephaly	0.001	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.001	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	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
M10.09 Idiopathic gout (Site unspecified)	0.002	0.998	0.000
D12.7 Rectosigmoid junction	0.002	0.998	0.000
Q21.8 Other congenital malformations of cardiac septa	0.002	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.998	0.000
Q51.3 Bicornate uterus	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.001	0.998	0.000
Q03 Congenital hydrocephalus	0.001	0.998	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
Q90 Down's syndrome	0.001	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
A41.5 Septicaemia due to other Gram-negative organisms	0.000	0.998	0.002
D47.9 Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified	0.000	0.998	0.002
F31.1 Bipolar affective disorder, current episode manic without psychotic symptoms	0.000	0.998	0.002
M67.2 Synovial hypertrophy, not elsewhere classified	0.000	0.998	0.002
Q28.9 Congenital malformation of circulatory system, unspecified	0.001	0.998	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.001	0.998	0.000
Q28.1 Other malformations of precerebral vessels	0.001	0.998	0.000
I99 Other and unspecified disorders of circulatory system	0.000	0.998	0.002
Q35 Cleft palate	0.001	0.998	0.000
D47.7 Other specified neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue	0.000	0.998	0.001
D47.5 Chronic eosinophilic leukaemia [hypereosinophilic syndrome]	0.000	0.998	0.001
D47.0 Histiocytic and mast cell tumours of uncertain and unknown behaviour	0.000	0.998	0.001
M10.0 Idiopathic gout	0.001	0.998	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.001	0.998	0.000
Q04 Other congenital malformations of brain	0.001	0.998	0.000
B34.3 Parvovirus infection, unspecified	0.000	0.998	0.001
B34.2 Coronavirus infection, unspecified	0.000	0.998	0.001
B34.1 Enterovirus infection, unspecified	0.000	0.998	0.001
B34.0 Adenovirus infection, unspecified	0.000	0.998	0.001
H05.2 Exophthalmic conditions	0.002	0.998	0.000
T39.0 Salicylates	0.002	0.998	0.000
T45.9 Primarily systemic and haematological agent, unspecified	0.001	0.998	0.000
T45.8 Other primarily systemic and haematological agents	0.001	0.998	0.000
T45.7 Anticoagulant antagonists, vitamin K and other coagulants	0.001	0.998	0.000
T45.6 Fibrinolysis-affecting drugs	0.001	0.998	0.000
T45.4 Iron and its compounds	0.001	0.998	0.000
T45.3 Enzymes, not elsewhere classified	0.001	0.998	0.000
N70.1 Chronic salpingitis and oophoritis	0.002	0.998	0.000
N76.3 Subacute and chronic vulvitis	0.001	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.001	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.001	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.001	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.001	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.001	0.998	0.000
Q64.4 Malformation of urachus	0.001	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.001	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.001	0.998	0.000
Q64.0 Epispadias	0.001	0.998	0.000
Q99.9 Chromosomal abnormality, unspecified	0.001	0.998	0.000
Q99.2 Fragile X chromosome	0.001	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.001	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.001	0.998	0.000
T39.9 Nonopioid analgesic, antipyretic and antirheumatic, unspecified	0.001	0.998	0.000
U80.0 Penicillin resistant agent	0.000	0.998	0.002
T47 Poisoning by agents primarily affecting gastro-intestinal system	0.002	0.998	0.000
S82.50 Fracture of medial malleolus (closed)	0.002	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
M94.29 Chondromalacia (Site unspecified)	0.000	0.998	0.001
M94.28 Chondromalacia (Other)	0.000	0.998	0.001
M94.27 Chondromalacia (Ankle and foot)	0.000	0.998	0.001
M94.25 Chondromalacia (Pelvic region and thigh)	0.000	0.998	0.001
M94.24 Chondromalacia (Hand)	0.000	0.998	0.001
M94.23 Chondromalacia (Forearm)	0.000	0.998	0.001
M94.22 Chondromalacia (Upper arm)	0.000	0.998	0.001
M94.21 Chondromalacia (Shoulder region)	0.000	0.998	0.001
M94.20 Chondromalacia (Multiple sites)	0.000	0.998	0.001
S52.01 Fracture of upper end of ulna (open)	0.001	0.998	0.000
D47.2 Monoclonal gammopathy	0.000	0.998	0.001
E14.3 With ophthalmic complications	0.000	0.998	0.002
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.001	0.998	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.001	0.998	0.000
Q20.6 Isomerism of atrial appendages	0.001	0.998	0.000
Q20.5 Discordant atrioventricular connexion	0.001	0.998	0.000
Q20.4 Double inlet ventricle	0.001	0.998	0.000
Q20.3 Discordant ventriculoarterial connexion	0.001	0.998	0.000
Q20.2 Double outlet left ventricle	0.001	0.998	0.000
Q20.1 Double outlet right ventricle	0.001	0.998	0.000
Q20.0 Common arterial trunk	0.001	0.998	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.001	0.998	0.000
Q26.8 Other congenital malformations of great veins	0.001	0.998	0.000
Q26.6 Portal vein-hepatic artery fistula	0.001	0.998	0.000
Q26.5 Anomalous portal venous connexion	0.001	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.001	0.998	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.001	0.998	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.001	0.998	0.000
Q26.1 Persistent left superior vena cava	0.001	0.998	0.000
Q26.0 Congenital stenosis of vena cava	0.001	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.001	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.001	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.001	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.001	0.998	0.000
Q98.5 Karyotype 47,XYY	0.001	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.001	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.001	0.998	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.001	0.998	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.001	0.998	0.000
S82.2 Fracture of shaft of tibia	0.000	0.998	0.001
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.001	0.998	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.001	0.998	0.000
Q22.6 Hypoplastic right heart syndrome	0.001	0.998	0.000
Q22.5 Ebstein's anomaly	0.001	0.998	0.000
Q22.4 Congenital tricuspid stenosis	0.001	0.998	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.001	0.998	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.001	0.998	0.000
Q22.0 Pulmonary valve atresia	0.001	0.998	0.000
H92 Otalgia and effusion of ear	0.000	0.998	0.001
M94 Other disorders of cartilage	0.000	0.998	0.001
Q27 Other congenital malformations of peripheral vascular system	0.001	0.998	0.000
M10.38 Gout due to impairment of renal function (Other)	0.001	0.999	0.000
M10.37 Gout due to impairment of renal function (Ankle and foot)	0.001	0.999	0.000
M10.36 Gout due to impairment of renal function (Lower leg)	0.001	0.999	0.000
M10.35 Gout due to impairment of renal function (Pelvic region and thigh)	0.001	0.999	0.000
M10.34 Gout due to impairment of renal function (Hand)	0.001	0.999	0.000
M10.33 Gout due to impairment of renal function (Forearm)	0.001	0.999	0.000
M10.32 Gout due to impairment of renal function (Upper arm)	0.001	0.999	0.000
M10.31 Gout due to impairment of renal function (Shoulder region)	0.001	0.999	0.000
M10.30 Gout due to impairment of renal function (Multiple sites)	0.001	0.999	0.000
H92.0 Otalgia	0.000	0.999	0.001
Q22.1 Congenital pulmonary valve stenosis	0.001	0.999	0.000
Q28.3 Other malformations of cerebral vessels	0.001	0.999	0.000
Q35.9 Cleft palate, unspecified	0.001	0.999	0.000
Q61.8 Other cystic kidney diseases	0.001	0.999	0.000
Q61.1 Polycystic kidney, infantile type	0.001	0.999	0.000
R93.5 Abnormal findings on diagnostic imaging of other abdominal regions, including retroperitoneum	0.000	0.999	0.001
T47.4 Other laxatives	0.001	0.999	0.000
Q34 Other congenital malformations of respiratory system	0.001	0.999	0.000
Q33 Congenital malformations of lung	0.001	0.999	0.000
Q32 Congenital malformations of trachea and bronchus	0.001	0.999	0.000
Q31 Congenital malformations of larynx	0.001	0.999	0.000
Q30 Congenital malformations of nose	0.001	0.999	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.001	0.999	0.000
M10.4 Other secondary gout	0.001	0.999	0.000
M10.2 Drug-induced gout	0.001	0.999	0.000
M10.1 Lead-induced gout	0.001	0.999	0.000
Q61.4 Renal dysplasia	0.001	0.999	0.000
Q62.1 Atresia and stenosis of ureter	0.001	0.999	0.000
Q96.9 Turner's syndrome, unspecified	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
Q38-Q45 Other congenital malformations of the digestive system	0.001	0.999	0.000
L72.0 Epidermal cyst	0.000	0.999	0.001
O14.0 Moderate preeclampsia	0.001	0.999	0.000
Q00.2 Iniencephaly	0.001	0.999	0.000
Q00.1 Craniorachischisis	0.001	0.999	0.000
Q00.0 Anencephaly	0.001	0.999	0.000
Q01.9 Encephalocele, unspecified	0.001	0.999	0.000
Q01.8 Encephalocele of other sites	0.001	0.999	0.000
Q01.2 Occipital encephalocele	0.001	0.999	0.000
Q01.1 Nasofrontal encephalocele	0.001	0.999	0.000
Q01.0 Frontal encephalocele	0.001	0.999	0.000
Q06.9 Congenital malformation of spinal cord, unspecified	0.001	0.999	0.000
Q06.8 Other specified congenital malformations of spinal cord	0.001	0.999	0.000
Q06.4 Hydromyelia	0.001	0.999	0.000
Q06.3 Other congenital cauda equina malformations	0.001	0.999	0.000
Q06.2 Diastematomyelia	0.001	0.999	0.000
Q06.1 Hypoplasia and dysplasia of spinal cord	0.001	0.999	0.000
Q06.0 Amyelia	0.001	0.999	0.000
Q62.8 Other congenital malformations of ureter	0.001	0.999	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.001	0.999	0.000
Q62.6 Malposition of ureter	0.001	0.999	0.000
Q62.4 Agenesis of ureter	0.001	0.999	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.001	0.999	0.000
Q62.2 Congenital megaloureter	0.001	0.999	0.000
Q62.0 Congenital hydronephrosis	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
F31.6 Bipolar affective disorder, current episode mixed	0.000	0.999	0.001
Q28.0 Arteriovenous malformation of precerebral vessels	0.001	0.999	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.999	0.000
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
T47.2 Stimulant laxatives	0.001	0.999	0.000
T88.7 Unspecified adverse effect of drug or medicament	0.000	0.999	0.001
F31 Bipolar affective disorder	0.000	0.999	0.001
Q05 Spina bifida	0.001	0.999	0.000
R34 Anuria and oliguria	0.001	0.999	0.000
M25.97 Joint disorder, unspecified (Ankle and foot)	0.000	0.999	0.001
M67.43 Ganglion, wrist	0.000	0.999	0.001
C49.2 Connective and soft tissue of lower limb, including hip	0.000	0.999	0.001
F31.3 Bipolar affective disorder, current episode mild or moderate depression	0.000	0.999	0.001
N32.3 Diverticulum of bladder	0.000	0.999	0.001
Q03.9 Congenital hydrocephalus, unspecified	0.001	0.999	0.000
Q03.8 Other congenital hydrocephalus	0.001	0.999	0.000
Q03.1 Atresia of foramina of Magendie and Luschka	0.001	0.999	0.000
Q21.4 Aortopulmonary septal defect	0.001	0.999	0.000
Q21.3 Tetralogy of Fallot	0.001	0.999	0.000
Q21.2 Atrioventricular septal defect	0.001	0.999	0.000
Q35.8 (Cleft palate, unspecified, bilateral)	0.001	0.999	0.000
Q35.7 Cleft uvula	0.001	0.999	0.000
Q35.6 Cleft palate, medial	0.001	0.999	0.000
Q35.5 Cleft hard palate with cleft soft palate	0.001	0.999	0.000
Q35.4 (Cleft hard palate with cleft soft palate, bilateral)	0.001	0.999	0.000
Q35.3 Cleft soft palate	0.001	0.999	0.000
Q35.2 (Cleft soft palate, bilateral)	0.001	0.999	0.000
Q35.1 Cleft hard palate	0.001	0.999	0.000
Q35.0 (Cleft hard palate, bilateral)	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
T93.8 Sequelae of other specified injuries of lower limb	0.001	0.999	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.001	0.999	0.000
Q84 Other congenital malformations of integument	0.001	0.999	0.000
Q81 Epidermolysis bullosa	0.001	0.999	0.000
Q80 Congenital ichthyosis	0.001	0.999	0.000
M10.08 Idiopathic gout (Other)	0.001	0.999	0.000
M10.06 Idiopathic gout (Lower leg)	0.001	0.999	0.000
M10.05 Idiopathic gout (Pelvic region and thigh)	0.001	0.999	0.000
M10.04 Idiopathic gout (Hand)	0.001	0.999	0.000
M10.03 Idiopathic gout (Forearm)	0.001	0.999	0.000
M10.02 Idiopathic gout (Upper arm)	0.001	0.999	0.000
M10.01 Idiopathic gout (Shoulder region)	0.001	0.999	0.000
E06.3 Autoimmune thyroiditis	0.000	0.999	0.001
F31.8 Other bipolar affective disorders	0.000	0.999	0.001
N76.8 Other specified inflammation of vagina and vulva	0.001	0.999	0.000
Q04.9 Congenital malformation of brain, unspecified	0.001	0.999	0.000
Q04.8 Other specified congenital malformations of brain	0.001	0.999	0.000
Q04.5 Megalencephaly	0.001	0.999	0.000
Q04.4 Septo-optic dysplasia	0.001	0.999	0.000
Q04.3 Other reduction deformities of brain	0.001	0.999	0.000
Q04.2 Holoprosencephaly	0.001	0.999	0.000
Q04.1 Arhinencephaly	0.001	0.999	0.000
Q04.0 Congenital malformations of corpus callosum	0.001	0.999	0.000
V18.2 Unspecified pedal cyclist injured in nontraffic accident	0.001	0.999	0.000
M10.00 Idiopathic gout (Multiple sites)	0.001	0.999	0.000
A02.0 Salmonella gastro-enteritis	0.001	0.999	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.001	0.999	0.000
Q90.9 Down's syndrome, unspecified	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