TreeWAS – Variant ID: rs11190164

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
I49.9 Cardiac arrhythmia, unspecified	0.803	0.197	0.000
I49 Other cardiac arrhythmias	0.793	0.207	0.000
I49.5 Sick sinus syndrome	0.783	0.217	0.000
I49.8 Other specified cardiac arrhythmias	0.745	0.255	0.000
I49.0 Ventricular fibrillation and flutter	0.665	0.335	0.000
I49.4 Other and unspecified premature depolarisation	0.629	0.371	0.000
I49.2 Junctional premature depolarisation	0.568	0.432	0.000
I49.1 Atrial premature depolarisation	0.560	0.440	0.000
I49.3 Ventricular premature depolarisation	0.270	0.730	0.000
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency	0.048	0.952	0.000
D51 Vitamin B12 deficiency anaemia	0.018	0.981	0.000
D51.8 Other vitamin B12 deficiency anaemias	0.013	0.986	0.000
D51.3 Other dietary vitamin B12 deficiency anaemia	0.013	0.986	0.000
D51.2 Transcobalamin II deficiency	0.013	0.986	0.000
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria	0.013	0.986	0.000
Z08.2 Follow-up examination after chemotherapy for malignant neoplasm	0.012	0.988	0.000
Q61.3 Polycystic kidney, unspecified	0.012	0.988	0.000
Y45.3 Other nonsteroidal anti-inflammatory drugs [NSAID]	0.000	0.989	0.011
Z22.3 Carrier of other specified bacterial diseases	0.000	0.989	0.011
D51.9 Vitamin B12 deficiency anaemia, unspecified	0.009	0.991	0.000
Z83.7 Family history of diseases of the digestive system	0.000	0.991	0.009
Q61 Cystic kidney disease	0.008	0.992	0.000
Z22 Carrier of infectious disease	0.000	0.993	0.007
Z83 Family history of other specific disorders	0.000	0.993	0.007
Z83.3 Family history of diabetes mellitus	0.000	0.993	0.007
D50-D53 Nutritional anaemias	0.007	0.993	0.000
Z22.5 Carrier of viral hepatitis	0.000	0.994	0.006
T85.7 Infection and inflammatory reaction due to other internal prosthetic devices, implants and grafts	0.006	0.994	0.000
Z83.1 Family history of other infectious and parasitic diseases	0.000	0.994	0.006
Q61.2 Polycystic kidney, adult type	0.006	0.994	0.000
Q61.5 Medullary cystic kidney	0.006	0.994	0.000
Q61.8 Other cystic kidney diseases	0.006	0.994	0.000
Q61.4 Renal dysplasia	0.006	0.994	0.000
Q61.1 Polycystic kidney, infantile type	0.006	0.994	0.000
Q61.0 Congenital single renal cyst	0.006	0.994	0.000
D52 Folate deficiency anaemia	0.006	0.994	0.000
Z22.1 Carrier of other intestinal infectious diseases	0.000	0.994	0.006
Z83.2 Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.000	0.994	0.006
D53 Other nutritional anaemias	0.006	0.994	0.000
Z22.8 Carrier of other infectious diseases	0.000	0.995	0.005
Z22.9 Carrier of infectious disease, unspecified	0.000	0.995	0.005
Z22.6 Carrier of human T-lymphotropic virus type 1 [HTLV-1] infection	0.000	0.995	0.005
Z22.4 Carrier of infections with a predominantly sexual mode of transmission	0.000	0.995	0.005
Z22.2 Carrier of diphtheria	0.000	0.995	0.005
Z22.0 Carrier of typhoid	0.000	0.995	0.005
Q60-Q64 Congenital malformations of the urinary system	0.005	0.995	0.000
D52.9 Folate deficiency anaemia, unspecified	0.005	0.995	0.000
Z83.6 Family history of diseases of the respiratory system	0.000	0.995	0.005
Z83.0 Family history of human immunodeficiency virus [HIV]	0.000	0.995	0.005
D53.9 Nutritional anaemia, unspecified	0.005	0.995	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.005	0.995	0.000
Z83.5 Family history of eye and ear disorders	0.000	0.995	0.005
Q61.9 Cystic kidney disease, unspecified	0.004	0.995	0.000
G71.3 Mitochondrial myopathy, not elsewhere classified	0.004	0.995	0.000
T85.5 Mechanical complication of gastro-intestinal prosthetic devices, implants and grafts	0.005	0.995	0.000
G70.0 Myasthenia gravis	0.004	0.996	0.000
Q62.5 Duplication of ureter	0.004	0.996	0.000
D52.8 Other folate deficiency anaemias	0.004	0.996	0.000
D52.1 Drug-induced folate deficiency anaemia	0.004	0.996	0.000
D52.0 Dietary folate deficiency anaemia	0.004	0.996	0.000
S30.9 Superficial injury of abdomen, lower back and pelvis, part unspecified	0.000	0.996	0.004
G70 Myasthenia gravis and other myoneural disorders	0.004	0.996	0.000
T85 Complications of other internal prosthetic devices, implants and grafts	0.004	0.996	0.000
D53.8 Other specified nutritional anaemias	0.004	0.996	0.000
D53.2 Scorbutic anaemia	0.004	0.996	0.000
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.004	0.996	0.000
D53.0 Protein deficiency anaemia	0.004	0.996	0.000
Q63 Other congenital malformations of kidney	0.004	0.996	0.000
R93.2 Abnormal findings on diagnostic imaging of liver and biliary tract	0.004	0.996	0.000
Q64 Other congenital malformations of urinary system	0.004	0.996	0.000
O20.0 Threatened abortion	0.004	0.996	0.000
T85.2 Mechanical complication of intraocular lens	0.004	0.996	0.000
G71 Primary disorders of muscles	0.004	0.996	0.000
G70.9 Myoneural disorder, unspecified	0.004	0.996	0.000
Q62.2 Congenital megaloureter	0.004	0.996	0.000
C18.0 Caecum	0.004	0.996	0.000
G70-G73 Diseases of myoneural junction and muscle	0.004	0.996	0.000
T85.6 Mechanical complication of other specified internal prosthetic devices, implants and grafts	0.004	0.996	0.000
Q62.8 Other congenital malformations of ureter	0.004	0.996	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.004	0.996	0.000
Q62.6 Malposition of ureter	0.004	0.996	0.000
Q62.4 Agenesis of ureter	0.004	0.996	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.004	0.996	0.000
Q62.1 Atresia and stenosis of ureter	0.004	0.996	0.000
Q62.0 Congenital hydronephrosis	0.004	0.996	0.000
T85.0 Mechanical complication of ventricular intracranial (communicating) shunt	0.004	0.996	0.000
Q63.8 Other specified congenital malformations of kidney	0.004	0.996	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.004	0.996	0.000
R93.3 Abnormal findings on diagnostic imaging of other parts of digestive tract	0.004	0.996	0.000
H16 Keratitis	0.004	0.996	0.000
R93.5 Abnormal findings on diagnostic imaging of other abdominal regions, including retroperitoneum	0.004	0.996	0.000
H16.1 Other superficial keratitis without conjunctivitis	0.004	0.996	0.000
R93 Abnormal findings on diagnostic imaging of other body structures	0.004	0.996	0.000
B98.0 Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters	0.000	0.997	0.003
Z83.4 Family history of other endocrine, nutritional and metabolic diseases	0.000	0.997	0.003
H16.0 Corneal ulcer	0.003	0.997	0.000
G70.8 Other specified myoneural disorders	0.003	0.997	0.000
G70.2 Congenital and developmental myasthenia	0.003	0.997	0.000
G70.1 Toxic myoneural disorders	0.003	0.997	0.000
Q63.0 Accessory kidney	0.003	0.997	0.000
G72 Other myopathies	0.003	0.997	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.003	0.997	0.000
Q63.3 Hyperplastic and giant kidney	0.003	0.997	0.000
G73 Disorders of myoneural junction and muscle in diseases classified elsewhere	0.003	0.997	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.003	0.997	0.000
Q64.8 Other specified congenital malformations of urinary system	0.003	0.997	0.000
Q64.6 Congenital diverticulum of bladder	0.003	0.997	0.000
Q64.5 Congenital absence of bladder and urethra	0.003	0.997	0.000
Q64.4 Malformation of urachus	0.003	0.997	0.000
Q64.2 Congenital posterior urethral valves	0.003	0.997	0.000
Q64.1 Exstrophy of urinary bladder	0.003	0.997	0.000
Q64.0 Epispadias	0.003	0.997	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.003	0.997	0.000
R93.0 Abnormal findings on diagnostic imaging of skull and head, not elsewhere classified	0.003	0.997	0.000
H18.8 Other specified disorders of cornea	0.003	0.997	0.000
N39.3 Stress incontinence	0.003	0.997	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.003	0.997	0.000
C34.9 Bronchus or lung, unspecified	0.003	0.997	0.000
G71.9 Primary disorder of muscle, unspecified	0.003	0.997	0.000
G71.8 Other primary disorders of muscles	0.003	0.997	0.000
G71.2 Congenital myopathies	0.003	0.997	0.000
H21.8 Other specified disorders of iris and ciliary body	0.003	0.997	0.000
D12.4 Descending colon	0.003	0.997	0.000
G71.1 Myotonic disorders	0.003	0.997	0.000
Q63.2 Ectopic kidney	0.003	0.997	0.000
H19 Disorders of sclera and cornea in diseases classified elsewhere	0.003	0.997	0.000
H16.4 Corneal neovascularisation	0.003	0.997	0.000
T85.1 Mechanical complication of implanted electronic stimulator of nervous system	0.003	0.997	0.000
N42.8 Other specified disorders of prostate	0.000	0.997	0.003
H16.2 Keratoconjunctivitis	0.003	0.997	0.000
H21 Other disorders of iris and ciliary body	0.003	0.997	0.000
R93.6 Abnormal findings on diagnostic imaging of limbs	0.003	0.997	0.000
G71.0 Muscular dystrophy	0.003	0.997	0.000
H21.2 Degeneration of iris and ciliary body	0.003	0.997	0.000
T85.8 Other complications of internal prosthetic devices, implants and grafts, not elsewhere classified	0.003	0.997	0.000
K29.8 Duodenitis	0.000	0.997	0.003
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.003	0.997	0.000
H15-H22 Disorders of sclera, cornea, iris and ciliary body	0.003	0.997	0.000
G73.7 Myopathy other diseases classified elsewhere	0.003	0.997	0.000
H19.1 Herpesviral keratitis and keratoconjunctivitis	0.003	0.997	0.000
R93.4 Abnormal findings on diagnostic imaging of urinary organs	0.003	0.997	0.000
G72.8 Other specified myopathies	0.003	0.997	0.000
G72.0 Drug-induced myopathy	0.003	0.997	0.000
W29.9 Unspecified place	0.000	0.997	0.003
H18 Other disorders of cornea	0.003	0.997	0.000
C34.3 Lower lobe, bronchus or lung	0.003	0.997	0.000
H16.8 Other keratitis	0.003	0.997	0.000
H16.3 Interstitial and deep keratitis	0.003	0.997	0.000
G72.1 Alcoholic myopathy	0.003	0.997	0.000
S30.1 Contusion of abdominal wall	0.000	0.997	0.003
M40.24 Other and unspecified kyphosis (Thoracic region)	0.003	0.997	0.000
H18.9 Disorder of cornea, unspecified	0.003	0.997	0.000
S30 Superficial injury of abdomen, lower back and pelvis	0.000	0.997	0.003
T93.3 Sequelae of dislocation, sprain and strain of lower limb	0.003	0.997	0.000
T85.9 Unspecified complication of internal prosthetic device, implant and graft	0.003	0.997	0.000
H19.3 Keratitis and keratoconjunctivitis in other diseases classified elsewhere	0.003	0.997	0.000
T85.3 Mechanical complication of other ocular prosthetic devices, imnplants and grafts	0.003	0.997	0.000
R93.8 Abnormal findings on diagnostic imaging of other specified body structures	0.003	0.997	0.000
H19.2 Keratitis and keratoconjunctivitis in other infectious and parasitic diseases classified elsewhere	0.003	0.997	0.000
G72.3 Periodic paralysis	0.003	0.997	0.000
G72.2 Myopathy due to other toxic agents	0.003	0.997	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.003	0.997	0.000
C34.2 Middle lobe, bronchus or lung	0.003	0.997	0.000
G73.6 Myopathy in metabolic diseases	0.002	0.997	0.000
G73.5 Myopathy in endocrine diseases	0.002	0.997	0.000
G73.4 Myopathy in infectious and parasitic diseases classified elsewhere	0.002	0.997	0.000
G73.3 Myasthenic syndromes in other diseases classified elsewhere	0.002	0.997	0.000
G73.2 Other myasthenic syndromes in neoplastic disease	0.002	0.997	0.000
G73.1 Eaton-Lambert syndrome	0.002	0.997	0.000
G73.0 Myasthenic syndromes in endocrine diseases	0.002	0.997	0.000
C34 Malignant neoplasm of bronchus and lung	0.003	0.997	0.000
G72.4 Inflammatory myopathy, not elsewhere classified	0.003	0.997	0.000
M25.76 Osteophyte (Lower leg)	0.000	0.997	0.003
H18.1 Bullous keratopathy	0.003	0.997	0.000
Q60.6 Potter's syndrome	0.002	0.997	0.000
Q60.5 Renal hypoplasia, unspecified	0.002	0.997	0.000
Q60.4 Renal hypoplasia, bilateral	0.002	0.997	0.000
Q60.3 Renal hypoplasia, unilateral	0.002	0.997	0.000
Q60.1 Renal agenesis, bilateral	0.002	0.997	0.000
H21.4 Pupillary membranes	0.002	0.997	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.003	0.997	0.000
H19.8 Other disorders of sclera and cornea in diseases classified elsewhere	0.002	0.997	0.000
H19.0 Scleritis and episcleritis in diseases classified elsewhere	0.002	0.997	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.003	0.997	0.000
H18.3 Changes in corneal membranes	0.002	0.997	0.000
H21.0 Hyphaema	0.002	0.997	0.000
K04.8 Radicular cyst	0.003	0.997	0.000
H21.3 Cyst of iris, ciliary body and anterior chamber	0.002	0.997	0.000
K26.5 Chronic or unspecified with perforation	0.000	0.998	0.002
T93.2 Sequelae of other fractures of lower limb	0.002	0.998	0.000
G72.9 Myopathy, unspecified	0.002	0.998	0.000
H16.9 Keratitis, unspecified	0.002	0.998	0.000
H21.9 Disorder of iris and ciliary body, unspecified	0.002	0.998	0.000
H21.1 Other vascular disorders of iris and ciliary body	0.002	0.998	0.000
M40.2 Other and unspecified kyphosis	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
T93.5 Sequelae of injury of muscle and tendon of lower limb	0.002	0.998	0.000
H18.7 Other corneal deformities	0.002	0.998	0.000
H18.0 Corneal pigmentations and deposits	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
Q66 Congenital deformities of feet	0.002	0.998	0.000
Q60.2 Renal agenesis, unspecified	0.002	0.998	0.000
M40.26 Other and unspecified kyphosis (Lumbar region)	0.002	0.998	0.000
H47.2 Optic atrophy	0.000	0.998	0.002
S30.7 Multiple superficial injuries of abdomen, lower back and pelvis	0.000	0.998	0.002
S30.0 Contusion of lower back and pelvis	0.000	0.998	0.002
Q43 Other congenital malformations of intestine	0.002	0.998	0.000
Q65 Congenital deformities of hip	0.002	0.998	0.000
C18.3 Hepatic flexure	0.002	0.998	0.000
H18.2 Other corneal oedema	0.002	0.998	0.000
H20 Iridocyclitis	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
Q67.5 Congenital deformity of spine	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
T93 Sequelae of injuries of lower limb	0.002	0.998	0.000
S30.8 Other superficial injuries of abdomen, lower back and pelvis	0.000	0.998	0.002
H17 Corneal scars and opacities	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
C34.8 Overlapping lesion of bronchus and lung	0.002	0.998	0.000
H22 Disorders of iris and ciliary body in diseases classified elsewhere	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
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
M40.29 Other and unspecified kyphosis (Site unspecified)	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
H53.8 Other visual disturbances	0.002	0.998	0.000
Q44.6 Cystic disease of liver	0.002	0.998	0.000
Q43.8 Other specified congenital malformations of intestine	0.002	0.998	0.000
G96.0 Cerebrospinal fluid leak	0.000	0.998	0.002
Q65.8 Other congenital deformities of hip	0.002	0.998	0.000
N11.9 Chronic tubulo-interstitial nephritis, unspecified	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q66.9 Congenital deformity of feet, unspecified	0.002	0.998	0.000
T93.8 Sequelae of other specified injuries of lower limb	0.002	0.998	0.000
Z43.3 Attention to colostomy	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
R40.2 Coma, unspecified	0.002	0.998	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
G56.3 Lesion of radial nerve	0.000	0.998	0.002
Q75 Other congenital malformations of skull and face bones	0.002	0.998	0.000
Q73 Reduction defects of unspecified limb	0.002	0.998	0.000
Q72 Reduction defects of lower limb	0.002	0.998	0.000
Q71 Reduction defects of upper limb	0.002	0.998	0.000
Q70 Syndactyly	0.002	0.998	0.000
Q69 Polydactyly	0.002	0.998	0.000
Q66.6 Other congenital valgus deformities of feet	0.002	0.998	0.000
T85.4 Mechanical complication of breast prosthesis and implant	0.002	0.998	0.000
C53.9 Cervix uteri, unspecified	0.000	0.998	0.002
H18.6 Keratoconus	0.002	0.998	0.000
Q39.4 Oesophageal web	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.002	0.998	0.000
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.002	0.998	0.000
Q60.0 Renal agenesis, unilateral	0.002	0.998	0.000
S30.2 Contusion of external genital organs	0.000	0.998	0.002
Q35 Cleft palate	0.002	0.998	0.000
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	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
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
M40.28 Other and unspecified kyphosis (Sacral and sacrococcygeal region)	0.002	0.998	0.000
M40.27 Other and unspecified kyphosis (Lumbosacral region)	0.002	0.998	0.000
M40.25 Other and unspecified kyphosis (Thoracolumbar region)	0.002	0.998	0.000
M40.23 Other and unspecified kyphosis (Cervicothoracic region)	0.002	0.998	0.000
M40.22 Other and unspecified kyphosis (Cervical region)	0.002	0.998	0.000
M40.21 Other and unspecified kyphosis (Occipito-atlanto-axial region)	0.002	0.998	0.000
M40.20 Other and unspecified kyphosis (Multiple sites in spine)	0.002	0.998	0.000
H20.0 Acute and subacute iridocyclitis	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.998	0.000
H15 Disorders of sclera	0.002	0.998	0.000
H20.1 Chronic iridocyclitis	0.002	0.998	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.002	0.998	0.000
Q04 Other congenital malformations of brain	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
H47.0 Disorders of optic nerve, not elsewhere classified	0.000	0.998	0.002
Q39.9 Congenital malformation of oesophagus, unspecified	0.002	0.998	0.000
Q39.8 Other congenital malformations of oesophagus	0.002	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.002	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.002	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.002	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.002	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.002	0.998	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.002	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.002	0.998	0.000
Q76 Congenital malformations of spine and bony thorax	0.002	0.998	0.000
Q66.7 Pes cavus	0.002	0.998	0.000
Q66.5 Congenital pes planus	0.002	0.998	0.000
Q66.4 Talipes calcaneovalgus	0.002	0.998	0.000
Q66.3 Other congenital varus deformities of feet	0.002	0.998	0.000
Q66.1 Talipes calcaneovarus	0.002	0.998	0.000
Q66.0 Talipes equinovarus	0.002	0.998	0.000
Q67.8 Other congenital deformities of chest	0.002	0.998	0.000
Q67.7 Pectus carinatum	0.002	0.998	0.000
Q67.3 Plagiocephaly	0.002	0.998	0.000
Q67.2 Dolichocephaly	0.002	0.998	0.000
Q67.1 Compression facies	0.002	0.998	0.000
Q67.0 Facial asymmetry	0.002	0.998	0.000
Q45.8 Other specified congenital malformations of digestive system	0.002	0.998	0.000
Q66.8 Other congenital deformities of feet	0.002	0.998	0.000
Q52 Other congenital malformations of female genitalia	0.002	0.998	0.000
H17.9 Corneal scar and opacity, unspecified	0.002	0.998	0.000
I82.9 Embolism and thrombosis of unspecified vein	0.000	0.998	0.002
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
Q65.9 Congenital deformity of hip, unspecified	0.002	0.998	0.000
Q65.6 Unstable hip	0.002	0.998	0.000
Q65.5 Congenital subluxation of hip, unspecified	0.002	0.998	0.000
Q65.4 Congenital subluxation of hip, bilateral	0.002	0.998	0.000
Q65.3 Congenital subluxation of hip, unilateral	0.002	0.998	0.000
Q65.2 Congenital dislocation of hip, unspecified	0.002	0.998	0.000
Q65.1 Congenital dislocation of hip, bilateral	0.002	0.998	0.000
Q65.0 Congenital dislocation of hip, unilateral	0.002	0.998	0.000
Z89.5 Acquired absence of leg at or below knee	0.002	0.998	0.000
H47 Other disorders of optic [2nd] nerve and visual pathways	0.000	0.998	0.002
H20.2 Lens-induced iridocyclitis	0.002	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.002	0.998	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.998	0.000
Q35.9 Cleft palate, unspecified	0.002	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.002	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.002	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.002	0.998	0.000
Q45.1 Annular pancreas	0.002	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.002	0.998	0.000
Q52.5 Fusion of labia	0.002	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.002	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.002	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.002	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.002	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.002	0.998	0.000
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
H17.1 Other central corneal opacity	0.002	0.998	0.000
H17.0 Adherent leukoma	0.002	0.998	0.000
O21.1 Hyperemesis gravidarum with metabolic disturbance	0.002	0.998	0.000
O44.0 Placenta praevia specified as without haemorrhage	0.000	0.998	0.002
Q67.6 Pectus excavatum	0.002	0.998	0.000
T93.6 Sequelae of crushing injury and traumatic amputation of lower limb	0.002	0.998	0.000
T93.4 Sequelae of injury of nerve of lower limb	0.002	0.998	0.000
Q37 Cleft palate with cleft lip	0.002	0.998	0.000
Q36 Cleft lip	0.002	0.998	0.000
Q96 Turner's syndrome	0.002	0.998	0.000
H22.8 Other disorders of iris and ciliary body in diseases classified elsewhere	0.002	0.998	0.000
H22.0 Iridocyclitis in infectious and parasitic diseases classified elsewhere	0.002	0.998	0.000
H47.3 Other disorders of optic disk	0.000	0.998	0.002
Q66.2 Metatarsus varus	0.002	0.998	0.000
O20 Haemorrhage in early pregnancy	0.002	0.998	0.000
Q06.8 Other specified congenital malformations of spinal cord	0.002	0.998	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.002	0.998	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.002	0.998	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.002	0.998	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.002	0.998	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.002	0.998	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.002	0.998	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.002	0.998	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.002	0.998	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.002	0.998	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.002	0.998	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.002	0.998	0.000
Q68.5 Congenital bowing of long bones of leg, unspecified	0.002	0.998	0.000
Q68.4 Congenital bowing of tibia and fibula	0.002	0.998	0.000
Q68.3 Congenital bowing of femur	0.002	0.998	0.000
Q68.2 Congenital deformity of knee	0.002	0.998	0.000
Q68.1 Congenital deformity of hand	0.002	0.998	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.002	0.998	0.000
Q52.4 Other congenital malformations of vagina	0.002	0.998	0.000
Z71.1 Person with feared complaint in whom no diagnosis is made	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
M86.96 Osteomyelitis, unspecified (Lower leg)	0.002	0.998	0.000
C34.0 Main bronchus	0.002	0.998	0.000
Q04.8 Other specified congenital malformations of brain	0.002	0.998	0.000
M89.55 Osteolysis (Pelvic region and thigh)	0.002	0.998	0.000
Q43.3 Congenital malformations of intestinal fixation	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
Q90 Down's syndrome	0.002	0.998	0.000
H35.3 Degeneration of macula and posterior pole	0.002	0.998	0.000
R93.1 Abnormal findings on diagnostic imaging of heart and coronary circulation	0.002	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.002	0.998	0.000
Q33 Congenital malformations of lung	0.002	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.002	0.998	0.000
Q31 Congenital malformations of larynx	0.002	0.998	0.000
Q30 Congenital malformations of nose	0.002	0.998	0.000
N36.0 Urethral fistula	0.000	0.998	0.002
Q69.9 Polydactyly, unspecified	0.002	0.998	0.000
Q69.2 Accessory toe(s)	0.002	0.998	0.000
Q69.1 Accessory thumb(s)	0.002	0.998	0.000
Q69.0 Accessory finger(s)	0.002	0.998	0.000
Q70.9 Syndactyly, unspecified	0.002	0.998	0.000
Q70.4 Polysyndactyly	0.002	0.998	0.000
Q70.3 Webbed toes	0.002	0.998	0.000
Q70.2 Fused toes	0.002	0.998	0.000
Q70.1 Webbed fingers	0.002	0.998	0.000
Q70.0 Fused fingers	0.002	0.998	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.002	0.998	0.000
Q71.8 Other reduction defects of upper limb(s)	0.002	0.998	0.000
Q71.6 Lobster-claw hand	0.002	0.998	0.000
Q71.5 Longitudinal reduction defect of ulna	0.002	0.998	0.000
Q71.4 Longitudinal reduction defect of radius	0.002	0.998	0.000
Q71.3 Congenital absence of hand and finger(s)	0.002	0.998	0.000
Q71.2 Congenital absence of both forearm and hand	0.002	0.998	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.002	0.998	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.002	0.998	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.002	0.998	0.000
Q72.8 Other reduction defects of lower limb(s)	0.002	0.998	0.000
Q72.7 Split foot	0.002	0.998	0.000
Q72.6 Longitudinal reduction defect of fibula	0.002	0.998	0.000
Q72.5 Longitudinal reduction defect of tibia	0.002	0.998	0.000
Q72.4 Longitudinal reduction defect of femur	0.002	0.998	0.000
Q72.3 Congenital absence of foot and toe(s)	0.002	0.998	0.000
Q72.2 Congenital absence of both lower leg and foot	0.002	0.998	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.002	0.998	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.002	0.998	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.002	0.998	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.002	0.998	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.002	0.998	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.002	0.998	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.002	0.998	0.000
Q75.5 Oculomandibular dysostosis	0.002	0.998	0.000
Q75.4 Mandibulofacial dysostosis	0.002	0.998	0.000
Q75.3 Macrocephaly	0.002	0.998	0.000
Q75.2 Hypertelorism	0.002	0.998	0.000
Q75.1 Craniofacial dysostosis	0.002	0.998	0.000
Q75.0 Craniosynostosis	0.002	0.998	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.002	0.998	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.002	0.998	0.000
Q77.6 Chondroectodermal dysplasia	0.002	0.998	0.000
Q77.5 Diastrophic dysplasia	0.002	0.998	0.000
Q77.4 Achondroplasia	0.002	0.998	0.000
Q77.3 Chondrodysplasia punctata	0.002	0.998	0.000
Q77.2 Short rib syndrome	0.002	0.998	0.000
Q77.1 Thanatophoric short stature	0.002	0.998	0.000
Q77.0 Achondrogenesis	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
N11.1 Chronic obstructive pyelonephritis	0.002	0.998	0.000
H21.5 Other adhesions and disruptions of iris and ciliary body	0.001	0.998	0.000
Q04.6 Congenital cerebral cysts	0.002	0.998	0.000
Q35.8 (Cleft palate, unspecified, bilateral)	0.001	0.998	0.000
Q35.7 Cleft uvula	0.001	0.998	0.000
Q35.6 Cleft palate, medial	0.001	0.998	0.000
Q35.5 Cleft hard palate with cleft soft palate	0.001	0.998	0.000
Q35.4 (Cleft hard palate with cleft soft palate, bilateral)	0.001	0.998	0.000
Q35.3 Cleft soft palate	0.001	0.998	0.000
Q35.2 (Cleft soft palate, bilateral)	0.001	0.998	0.000
Q35.1 Cleft hard palate	0.001	0.998	0.000
Q35.0 (Cleft hard palate, bilateral)	0.001	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
Q43.0 Meckel's diverticulum	0.002	0.998	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.002	0.998	0.000
Q78.8 Other specified osteochondrodysplasias	0.002	0.998	0.000
Q78.6 Multiple congenital exostoses	0.002	0.998	0.000
Q78.5 Metaphyseal dysplasia	0.002	0.998	0.000
Q78.4 Enchondromatosis	0.002	0.998	0.000
Q78.3 Progressive diaphyseal dysplasia	0.002	0.998	0.000
Q78.2 Osteopetrosis	0.002	0.998	0.000
Q78.1 Polyostotic fibrous dysplasia	0.002	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
F22.0 Delusional disorder	0.000	0.998	0.002
H20.9 Iridocyclitis, unspecified	0.002	0.998	0.000
Q38.8 Other congenital malformations of pharynx	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
R93.7 Abnormal findings on diagnostic imaging of other parts of musculoskeletal system	0.002	0.998	0.000
X78.0 Home	0.000	0.998	0.002
M19.17 Post-traumatic arthrosis of other joints (Ankle and foot)	0.002	0.998	0.000
H15.9 Disorder of sclera, unspecified	0.001	0.998	0.000
Q51.8 Other congenital malformations of uterus and cervix	0.002	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

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