TreeWAS – Variant ID: rs1052536

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
H52.0 Hypermetropia	0.015	0.985	0.000
I51.9 Heart disease, unspecified	0.000	0.987	0.013
E05.0 Thyrotoxicosis with diffuse goitre	0.012	0.988	0.000
Z11.0 Special screening examination for intestinal infectious diseases	0.000	0.990	0.010
D05.1 Intraductal carcinoma in situ	0.009	0.991	0.000
S80.8 Other superficial injuries of lower leg	0.009	0.991	0.000
L72.8 Other follicular cysts of skin and subcutaneous tissue	0.000	0.991	0.009
Z97.4 Presence of external hearing-aid	0.008	0.992	0.000
L91.8 Other hypertrophic disorders of skin	0.007	0.993	0.000
E05 Thyrotoxicosis [hyperthyroidism]	0.006	0.994	0.000
K43.9 Ventral hernia without obstruction or gangrene	0.006	0.994	0.000
K59.9 Functional intestinal disorder, unspecified	0.005	0.995	0.000
R41.8 Other and unspecified symptoms and signs involving cognitive functions and awareness	0.005	0.995	0.000
R09.2 Respiratory arrest	0.000	0.995	0.005
E05.9 Thyrotoxicosis, unspecified	0.005	0.995	0.000
E05.1 Thyrotoxicosis with toxic single thyroid nodule	0.005	0.995	0.000
M21.07 Valgus deformity, not elsewhere classified (Ankle and foot)	0.000	0.995	0.005
E05.5 Thyroid crisis or storm	0.004	0.996	0.000
E05.4 Thyrotoxicosis factitia	0.004	0.996	0.000
E05.3 Thyrotoxicosis from ectopic thyroid tissue	0.004	0.996	0.000
N12 Tubulo-interstitial nephritis, not specified as acute or chronic	0.000	0.996	0.004
E05.8 Other thyrotoxicosis	0.004	0.996	0.000
H53.8 Other visual disturbances	0.004	0.996	0.000
Z11 Special screening examination for infectious and parasitic diseases	0.000	0.996	0.004
J93.1 Other spontaneous pneumothorax	0.004	0.996	0.000
E55.9 Vitamin D deficiency, unspecified	0.004	0.996	0.000
L27.0 Generalised skin eruption due to drugs and medicaments	0.004	0.996	0.000
S52.80 Fracture of other parts of forearm (closed)	0.004	0.996	0.000
J86.9 Pyothorax without fistula	0.000	0.996	0.004
E05.2 Thyrotoxicosis with toxic multinodular goitre	0.004	0.996	0.000
Z11.9 Special screening examination for infectious and parasitic diseases, unspecified	0.000	0.996	0.004
C18.5 Splenic flexure	0.000	0.996	0.004
S80 Superficial injury of lower leg	0.004	0.996	0.000
S80.0 Contusion of knee	0.003	0.997	0.000
Z97.8 Presence of other specified devices	0.003	0.997	0.000
K59.8 Other specified functional intestinal disorders	0.003	0.997	0.000
M66.06 Rupture of popliteal cyst-Lower leg	0.000	0.997	0.003
Z11.2 Special screening examination for other bacterial diseases	0.000	0.997	0.003
S80.7 Multiple superficial injuries of lower leg	0.003	0.997	0.000
Z11.6 Special screening examination for other protozoal diseases and helminthiases	0.000	0.997	0.003
Z11.3 Special screening examination for infections with a predominantly sexual mode of transmission	0.000	0.997	0.003
Z11.8 Special screening examination for other infectious and parasitic diseases	0.000	0.997	0.003
I80.8 Phlebitis and thrombophlebitis of other sites	0.003	0.997	0.000
L91 Hypertrophic disorders of skin	0.003	0.997	0.000
Z11.1 Special screening examination for respiratory tuberculosis	0.000	0.997	0.003
K59 Other functional intestinal disorders	0.003	0.997	0.000
M79.79 Fibromyalgia (Site unspecified)	0.003	0.997	0.000
Z11.4 Special screening examination for human immunodeficiency virus [HIV]	0.000	0.997	0.003
K59.4 Anal spasm	0.003	0.997	0.000
C43.4 Malignant melanoma of scalp and neck	0.003	0.997	0.000
W25.9 Unspecified place	0.003	0.997	0.000
Q38.7 Pharyngeal pouch	0.003	0.997	0.000
C45.0 Mesothelioma of pleura	0.000	0.997	0.003
D17.9 Benign lipomatous neoplasm, unspecified	0.003	0.997	0.000
M21.0 Valgus deformity, not elsewhere classified	0.000	0.997	0.003
D23.6 Skin of upper limb, including shoulder	0.000	0.997	0.003
Z97 Presence of other devices	0.003	0.997	0.000
C84.4 Peripheral T-cell lymphoma	0.000	0.997	0.003
G44.4 Drug-induced headache, not elsewhere classified	0.000	0.997	0.003
Q44.6 Cystic disease of liver	0.003	0.997	0.000
Z11.5 Special screening examination for other viral diseases	0.000	0.997	0.002
D14.0 Middle ear, nasal cavity and accessory sinuses	0.003	0.997	0.000
K59.2 Neurogenic bowel, not elsewhere classified	0.002	0.997	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.003	0.997	0.000
L91.0 Keloid scar	0.002	0.997	0.000
M21.06 Valgus deformity, not elsewhere classified (Lower leg)	0.000	0.998	0.002
G72.8 Other specified myopathies	0.002	0.998	0.000
L91.9 Hypertrophic disorder of skin, unspecified	0.002	0.998	0.000
G72.4 Inflammatory myopathy, not elsewhere classified	0.002	0.998	0.000
Q82.5 Congenital nonneoplastic naevus	0.002	0.998	0.000
E55 Vitamin D deficiency	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
G72.9 Myopathy, unspecified	0.002	0.998	0.000
I35.0 Aortic (valve) stenosis	0.000	0.998	0.002
M75.0 Adhesive capsulitis of shoulder	0.002	0.998	0.000
E03.8 Other specified hypothyroidism	0.002	0.998	0.000
M21.09 Valgus deformity, not elsewhere classified (Site unspecified)	0.000	0.998	0.002
M21.08 Valgus deformity, not elsewhere classified (Other)	0.000	0.998	0.002
M21.05 Valgus deformity, not elsewhere classified (Pelvic region and thigh)	0.000	0.998	0.002
M21.04 Valgus deformity, not elsewhere classified (Hand)	0.000	0.998	0.002
M21.03 Valgus deformity, not elsewhere classified (Forearm)	0.000	0.998	0.002
M21.02 Valgus deformity, not elsewhere classified (Upper arm)	0.000	0.998	0.002
M21.01 Valgus deformity, not elsewhere classified (Shoulder region)	0.000	0.998	0.002
M21.00 Valgus deformity, not elsewhere classified (Multiple sites)	0.000	0.998	0.002
R11 Nausea and vomiting	0.002	0.998	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.002	0.998	0.000
C84.5 Other and unspecified T-cell lymphomas	0.000	0.998	0.002
Q38.8 Other congenital malformations of pharynx	0.002	0.998	0.000
Z97.0 Presence of artificial eye	0.002	0.998	0.000
M66.0 Rupture of popliteal cyst	0.000	0.998	0.002
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
Z97.3 Presence of spectacles and contact lenses	0.002	0.998	0.000
G72 Other myopathies	0.002	0.998	0.000
I08.3 Combined disorders of mitral, aortic and tricuspid valves	0.000	0.998	0.002
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
Q66.8 Other congenital deformities of feet	0.002	0.998	0.000
C45.9 Mesothelioma, unspecified	0.000	0.998	0.002
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.998	0.000
Q38.1 Ankyloglossia	0.002	0.998	0.000
C53.0 Endocervix	0.002	0.998	0.000
Q07.0 Arnold-Chiari syndrome	0.002	0.998	0.000
M79.63 Pain in limb (Forearm)	0.000	0.998	0.002
I35.9 Aortic valve disorder, unspecified	0.000	0.998	0.002
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
C84 Peripheral and cutaneous T-cell lymphomas	0.000	0.998	0.002
Q55 Other congenital malformations of male genital organs	0.002	0.998	0.000
G51.9 Disorder of facial nerve, unspecified	0.002	0.998	0.000
I80.0 Phlebitis and thrombophlebitis of superficial vessels of lower extremities	0.002	0.998	0.000
S80.1 Contusion of other and unspecified parts of lower leg	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
S02.40 Fracture of malar and maxillary bones (closed)	0.000	0.998	0.002
K59.0 Constipation	0.002	0.998	0.000
Q55.6 Other congenital malformations of penis	0.002	0.998	0.000
E55.0 Rickets, active	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
C45 Mesothelioma	0.000	0.998	0.002
I51.0 Cardiac septal defect, acquired	0.000	0.998	0.002
Q82 Other congenital malformations of skin	0.002	0.998	0.000
H34.2 Other retinal artery occlusions	0.000	0.998	0.002
I80.9 Phlebitis and thrombophlebitis of unspecified site	0.002	0.998	0.000
K59.3 Megacolon, not elsewhere classified	0.002	0.998	0.000
S86.9 Injury of unspecified muscle and tendon at lower leg level	0.002	0.998	0.000
C84.0 Mycosis fungoides	0.000	0.998	0.002
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
H52 Disorders of refraction and accommodation	0.002	0.998	0.000
C14.0 Pharynx, unspecified	0.002	0.998	0.000
I35.8 Other aortic valve disorders	0.000	0.998	0.002
Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate	0.002	0.998	0.000
M25.47 Effusion of joint (Ankle and foot)	0.002	0.998	0.000
C43.7 Malignant melanoma of lower limb, including hip	0.002	0.998	0.000
M66.09 Rupture of popliteal cyst-Site unspec	0.000	0.998	0.002
M66.08 Rupture of popliteal cyst-Other	0.000	0.998	0.002
M66.07 Rupture of popliteal cyst-Ankle/foot	0.000	0.998	0.002
M66.05 Rupture of popliteal cyst-Pelvic/thigh	0.000	0.998	0.002
M66.04 Rupture of popliteal cyst-Hand	0.000	0.998	0.002
M66.03 Rupture of popliteal cyst-Forearm	0.000	0.998	0.002
M66.02 Rupture of popliteal cyst-Upper arm	0.000	0.998	0.002
M66.01 Rupture of popliteal cyst-Shldr region	0.000	0.998	0.002
M66.00 Rupture of popliteal cyst-Mult sites	0.000	0.998	0.002
G72.3 Periodic paralysis	0.002	0.998	0.000
G72.2 Myopathy due to other toxic agents	0.002	0.998	0.000
S52.8 Fracture of other parts of forearm	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
N32.9 Bladder disorder, unspecified	0.000	0.998	0.002
Z88.9 Personal history of allergy to unspecified drugs, medicaments and biological substances	0.002	0.998	0.000
G72.1 Alcoholic myopathy	0.002	0.998	0.000
K59.1 Functional diarrhoea	0.002	0.998	0.000
Z97.1 Presence of artificial limb (complete)(partial)	0.002	0.998	0.000
M46.92 Inflammatory spondylopathy, unspecified (Cervical region)	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
Q82.8 Other specified congenital malformations of skin	0.002	0.998	0.000
C84.9 Mature T/NK-cell lymphoma, unspecified	0.000	0.998	0.002
C84.8 Cutaneous T-cell lymphoma, unspecified	0.000	0.998	0.002
C84.7 Anaplastic large cell lymphoma, ALK-negative	0.000	0.998	0.002
C84.6 Anaplastic large cell lymphoma, ALK-positive	0.000	0.998	0.002
C84.3 Lymphoepithelioid lymphoma	0.000	0.998	0.002
C84.2 T-zone lymphoma	0.000	0.998	0.002
C84.1 Sezary's diease	0.000	0.998	0.002
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
Q55.3 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
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
H57.9 Disorder of eye and adnexa, unspecified	0.002	0.998	0.000
M94.96 Disorder of cartilage, unspecified (Lower leg)	0.002	0.998	0.000
K43 Ventral hernia	0.002	0.998	0.000
C45.7 Mesothelioma of other sites	0.000	0.998	0.002
C45.2 Mesothelioma of pericardium	0.000	0.998	0.002
C45.1 Mesothelioma of peritoneum	0.000	0.998	0.002
I35 Nonrheumatic aortic valve disorders	0.000	0.998	0.002
G44.2 Tension-type headache	0.000	0.998	0.002
Q82.9 Congenital malformation of skin, unspecified	0.001	0.998	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.001	0.998	0.000
Q82.3 Incontinentia pigmenti	0.001	0.998	0.000
Q82.1 Xeroderma pigmentosum	0.001	0.998	0.000
B17.1 Acute hepatitis C	0.002	0.998	0.000
Z97.2 Presence of dental prosthetic device (complete)(partial)	0.001	0.998	0.000
H52.6 Other disorders of refraction	0.001	0.998	0.000
H52.5 Disorders of accommodation	0.001	0.998	0.000
M79.7 Fibromyalgia	0.002	0.998	0.000
Q82.2 Mastocytosis	0.001	0.998	0.000
W25 Contact with sharp glass	0.002	0.998	0.000
M25.75 Osteophyte (Pelvic region and thigh)	0.000	0.998	0.002
Q07.8 Other specified congenital malformations of nervous system	0.001	0.998	0.000
Z99.1 Dependence on respirator	0.000	0.998	0.002
I80 Phlebitis and thrombophlebitis	0.002	0.998	0.000
L27 Dermatitis due to substances taken internally	0.002	0.998	0.000
M40.24 Other and unspecified kyphosis (Thoracic region)	0.002	0.998	0.000
S52.81 Fracture of other parts of forearm (open)	0.001	0.998	0.000
S05.8 Other injuries of eye and orbit	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	0.001	0.998	0.000
Q61 Cystic kidney disease	0.002	0.998	0.000
H52.7 Disorder of refraction, unspecified	0.001	0.998	0.000
Q39.8 Other congenital malformations of oesophagus	0.001	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.001	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.001	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.001	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.001	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.001	0.998	0.000
W25.8 Other specified place	0.001	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
D68.2 Hereditary deficiency of other clotting factors	0.000	0.998	0.002
H35.6 Retinal haemorrhage	0.000	0.998	0.002
Q82.0 Hereditary lymphoedema	0.001	0.998	0.000
Q87.4 Marfan's syndrome	0.001	0.998	0.000
G44 Other headache syndromes	0.000	0.998	0.002
M79.67 Pain in limb (Ankle and foot)	0.000	0.998	0.002
C71.2 Temporal lobe	0.002	0.998	0.000
K55.9 Vascular disorder of intestine, unspecified	0.000	0.998	0.002
Q07.9 Congenital malformation of nervous system, unspecified	0.001	0.998	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.001	0.998	0.000
D05 Carcinoma in situ of breast	0.002	0.998	0.000
H52.4 Presbyopia	0.001	0.998	0.000
H53.0 Amblyopia ex anopsia	0.002	0.998	0.000
Q39.4 Oesophageal web	0.001	0.998	0.000
Q62.2 Congenital megaloureter	0.001	0.998	0.000
R44.1 Visual hallucinations	0.000	0.998	0.002
S56.1 Injury of flexor muscle and tendon of other finger(s) at forearm level	0.000	0.998	0.001
J86 Pyothorax	0.000	0.998	0.001
M79.10 Myalgia (Multiple sites)	0.000	0.998	0.001
H52.2 Astigmatism	0.001	0.998	0.000
Q25.1 Coarctation of aorta	0.001	0.998	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.001	0.998	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.001	0.998	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.001	0.998	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.001	0.998	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.001	0.998	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.001	0.998	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.001	0.998	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.001	0.998	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.001	0.998	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.001	0.998	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.001	0.998	0.000
Q61.5 Medullary cystic kidney	0.001	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.001	0.998	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.001	0.998	0.000
I35.2 Aortic (valve) stenosis with insufficiency	0.000	0.999	0.001
O64.0 Obstructed labour due to incomplete rotation of foetal head	0.001	0.999	0.000
Q62.5 Duplication of ureter	0.001	0.999	0.000
M79.70 Fibromyalgia (Multiple sites)	0.001	0.999	0.000
E83.1 Disorders of iron metabolism	0.000	0.999	0.001
G72.0 Drug-induced myopathy	0.001	0.999	0.000
J84.9 Interstitial pulmonary disease, unspecified	0.001	0.999	0.000
K43.7 Other and unspecified ventral hernia with gangrene	0.001	0.999	0.000
K43.6 Other and unspecified ventral hernia with obstruction, without gangrene	0.001	0.999	0.000
K43.5 Parastomal hernia without obstruction or gangrene	0.001	0.999	0.000
K43.4 Parastomal hernia with gangrene	0.001	0.999	0.000
K43.3 Parastomal hernia with obstruction, without gangrene	0.001	0.999	0.000
K43.2 Incisional hernia without obstruction or gangrene	0.001	0.999	0.000
F60.8 Other specific personality disorders	0.001	0.999	0.000
I82.8 Embolism and thrombosis of other specified veins	0.000	0.999	0.001
Q40 Other congenital malformations of upper alimentary tract	0.001	0.999	0.000
Q00-Q07 Congenital malformations of the nervous system	0.001	0.999	0.000
F60.3 Emotionally unstable personality disorder	0.001	0.999	0.000
I80.1 Phlebitis and thrombophlebitis of femoral vein	0.001	0.999	0.000
K43.1 Ventral hernia with gangrene	0.001	0.999	0.000
S56.4 Injury of extensor muscle and tendon of other finger(s) at forearm level	0.000	0.999	0.001
W25.6 Industrial and construction area	0.001	0.999	0.000
W25.5 Trade and service area	0.001	0.999	0.000
W25.1 Residential institution	0.001	0.999	0.000
W25.0 Home	0.001	0.999	0.000
W25.7 Farm	0.001	0.999	0.000
W25.4 Street and highway	0.001	0.999	0.000
W25.3 Sports and athletics area	0.001	0.999	0.000
W25.2 School, other institution and public administrative area	0.001	0.999	0.000
Q89 Other congenital malformations, not elsewhere classified	0.001	0.999	0.000
M79.78 Fibromyalgia (Other)	0.001	0.999	0.000
M79.77 Fibromyalgia (Ankle and foot)	0.001	0.999	0.000
M79.76 Fibromyalgia (Lower leg)	0.001	0.999	0.000
M79.75 Fibromyalgia (Pelvic region and thigh)	0.001	0.999	0.000
M79.74 Fibromyalgia (Hand)	0.001	0.999	0.000
M79.73 Fibromyalgia (Forearm)	0.001	0.999	0.000
M79.72 Fibromyalgia (Upper arm)	0.001	0.999	0.000
M79.71 Fibromyalgia (Shoulder region)	0.001	0.999	0.000
G44.3 Chronic posttraumatic headache	0.000	0.999	0.001
L27.9 Dermatitis due to unspecified substance taken internally	0.001	0.999	0.000
L27.8 Dermatitis due to other substances taken internally	0.001	0.999	0.000
S56.3 Injury of extensor or abductor muscles and tendons of thumb at forearm level	0.000	0.999	0.001
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.001	0.999	0.000
S27.20 Traumatic haemopneumothorax (without open wound into thoracic cavity)	0.000	0.999	0.001
C53.9 Cervix uteri, unspecified	0.001	0.999	0.000
Q25.6 Stenosis of pulmonary artery	0.001	0.999	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.001	0.999	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.001	0.999	0.000
Q45.2 Congenital pancreatic cyst	0.001	0.999	0.000
Q45.1 Annular pancreas	0.001	0.999	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	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
Q04 Other congenital malformations of brain	0.001	0.999	0.000
M40.26 Other and unspecified kyphosis (Lumbar region)	0.001	0.999	0.000
F60.5 Anankastic personality disorder	0.001	0.999	0.000
L27.2 Dermatitis due to ingested food	0.001	0.999	0.000
M40.2 Other and unspecified kyphosis	0.001	0.999	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.001	0.999	0.000
F60 Specific personality disorders	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
M40.22 Other and unspecified kyphosis (Cervical region)	0.001	0.999	0.000
S27.80 Injury of other specified intrathoracic organs (without open wound into thoracic cavity)	0.000	0.999	0.001
G44.1 Vascular headache, not elsewhere classified	0.000	0.999	0.001
N27.0 Small kidney, unilateral	0.001	0.999	0.000
Q04.8 Other specified congenital malformations of brain	0.001	0.999	0.000
Q83 Congenital malformations of breast	0.001	0.999	0.000
S86 Injury of muscle and tendon at lower leg level	0.001	0.999	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.001	0.999	0.000
Q50-Q56 Congenital malformations of genital organs	0.001	0.999	0.000
G51.3 Clonic hemifacial spasm	0.001	0.999	0.000
H34.8 Other retinal vascular occlusions	0.000	0.999	0.001
I79.2 Peripheral angiopathy in diseases classified elsewhere	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
Q62.1 Atresia and stenosis of ureter	0.001	0.999	0.000
Q62.0 Congenital hydronephrosis	0.001	0.999	0.000
R23.4 Changes in skin texture	0.001	0.999	0.000
R26.2 Difficulty in walking, not elsewhere classified	0.001	0.999	0.000
Q96 Turner's syndrome	0.001	0.999	0.000
Q60-Q64 Congenital malformations of the urinary system	0.001	0.999	0.000
E61.2 Magnesium deficiency	0.001	0.999	0.000
N99.0 Postprocedural renal failure	0.000	0.999	0.001
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.001	0.999	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.001	0.999	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.001	0.999	0.000
Q96.9 Turner's syndrome, unspecified	0.001	0.999	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.001	0.999	0.000
F60.2 Dissocial personality disorder	0.001	0.999	0.000
G51.0 Bell's palsy	0.001	0.999	0.000
M17.0 Primary gonarthrosis, bilateral	0.001	0.999	0.000
Q51.4 Unicornate uterus	0.001	0.999	0.000
Q61.9 Cystic kidney disease, unspecified	0.001	0.999	0.000
Q89.2 Congenital malformations of other endocrine glands	0.001	0.999	0.000
Q35-Q37 Cleft lip and cleft palate	0.001	0.999	0.000
M79.69 Pain in limb (Site unspecified)	0.000	0.999	0.001
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.999	0.000
Q40.1 Congenital hiatus hernia	0.001	0.999	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.001	0.999	0.000
Q61.4 Renal dysplasia	0.001	0.999	0.000
Q61.2 Polycystic kidney, adult type	0.001	0.999	0.000
Q66.9 Congenital deformity of feet, unspecified	0.001	0.999	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.001	0.999	0.000
Q89.9 Congenital malformation, unspecified	0.001	0.999	0.000
Q89.8 Other specified congenital malformations	0.001	0.999	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.001	0.999	0.000
Q89.4 Conjoined twins	0.001	0.999	0.000
Q89.3 Situs inversus	0.001	0.999	0.000
Q89.1 Congenital malformations of adrenal gland	0.001	0.999	0.000
Q89.0 Congenital malformations of spleen	0.001	0.999	0.000
R79.9 Abnormal finding of blood chemistry, unspecified	0.001	0.999	0.000
Q06 Other congenital malformations of spinal cord	0.001	0.999	0.000
Q01 Encephalocele	0.001	0.999	0.000
Q00 Anencephaly and similar malformations	0.001	0.999	0.000
Q02 Microcephaly	0.001	0.999	0.000
Q31 Congenital malformations of larynx	0.001	0.999	0.000
Q66 Congenital deformities of feet	0.001	0.999	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.001	0.999	0.000
W25.09 Contact with sharp glass; Home; During unspecified activity	0.001	0.999	0.000
W25.03 Contact with sharp glass; Home; While engaged in other types of work	0.001	0.999	0.000
W25.18 Contact with sharp glass; Residential institution;While engaged in other specified activities	0.001	0.999	0.000
W25.52 Contact with sharp glass; Trade and service area;While working for income	0.001	0.999	0.000
W25.62 Contact with sharp glass; Industrial and construction area ;While working for income	0.001	0.999	0.000
E03.1 Congenital hypothyroidism without goitre	0.001	0.999	0.000
F60.7 Dependent personality disorder	0.001	0.999	0.000
J85.2 Abscess of lung without pneumonia	0.001	0.999	0.000
L27.1 Localised skin eruption due to drugs and medicaments	0.001	0.999	0.000
Q31.0 Web of larynx	0.001	0.999	0.000
C53 Malignant neoplasm of cervix uteri	0.001	0.999	0.000
G51 Facial nerve disorders	0.001	0.999	0.000
Q37 Cleft palate with cleft lip	0.001	0.999	0.000
M40.25 Other and unspecified kyphosis (Thoracolumbar region)	0.001	0.999	0.000
F60.4 Histrionic personality disorder	0.001	0.999	0.000
F60.1 Schizoid personality disorder	0.001	0.999	0.000
G44.8 Other specified headache syndromes	0.000	0.999	0.001
H35.8 Other specified retinal disorders	0.000	0.999	0.001
Q04.9 Congenital malformation of brain, unspecified	0.001	0.999	0.000
Q04.6 Congenital cerebral cysts	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
Q37.9 Unspecified cleft palate with unilateral cleft lip	0.001	0.999	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.999	0.000
Q80.9 Congenital ichthyosis, unspecified	0.001	0.999	0.000
Q80.8 Other congenital ichthyosis	0.001	0.999	0.000
Q80.4 Harlequin foetus	0.001	0.999	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.001	0.999	0.000
Q80.2 Lamellar ichthyosis	0.001	0.999	0.000
Q80.1 X-linked ichthyosis	0.001	0.999	0.000
Q80.0 Ichthyosis vulgaris	0.001	0.999	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.001	0.999	0.000
Q81.8 Other epidermolysis bullosa	0.001	0.999	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.001	0.999	0.000
Q81.1 Epidermolysis bullosa letalis	0.001	0.999	0.000
Q81.0 Epidermolysis bullosa simplex	0.001	0.999	0.000
Q83.1 Accessory breast	0.001	0.999	0.000
Q84.9 Congenital malformation of integument, unspecified	0.001	0.999	0.000
Q84.8 Other specified congenital malformations of integument	0.001	0.999	0.000
Q84.6 Other congenital malformations of nails	0.001	0.999	0.000
Q84.5 Enlarged and hypertrophic nails	0.001	0.999	0.000
Q84.4 Congenital leukonychia	0.001	0.999	0.000
Q84.3 Anonychia	0.001	0.999	0.000
Q84.2 Other congenital malformations of hair	0.001	0.999	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.001	0.999	0.000
Q84.0 Congenital alopecia	0.001	0.999	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.001	0.999	0.000
Q86.2 Dysmorphism due to warfarin	0.001	0.999	0.000
Q86.1 Foetal hydantoin syndrome	0.001	0.999	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.001	0.999	0.000
W21.9 Unspecified place	0.000	0.999	0.001
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.001	0.999	0.000
M40.28 Other and unspecified kyphosis (Sacral and sacrococcygeal region)	0.001	0.999	0.000
M40.27 Other and unspecified kyphosis (Lumbosacral region)	0.001	0.999	0.000
M40.23 Other and unspecified kyphosis (Cervicothoracic region)	0.001	0.999	0.000
M40.21 Other and unspecified kyphosis (Occipito-atlanto-axial region)	0.001	0.999	0.000
M40.20 Other and unspecified kyphosis (Multiple sites in spine)	0.001	0.999	0.000
C09.9 Tonsil, unspecified	0.001	0.999	0.000
Q45.8 Other specified congenital malformations of digestive system	0.001	0.999	0.000
Q83.9 Congenital malformation of breast, unspecified	0.001	0.999	0.000
Q83.3 Accessory nipple	0.001	0.999	0.000
Q83.2 Absent nipple	0.001	0.999	0.000
Q83.0 Congenital absence of breast with absent nipple	0.001	0.999	0.000
S86.0 Injury of Achilles tendon	0.001	0.999	0.000
S86.7 Injury of multiple muscles and tendons at lower leg level	0.001	0.999	0.000
S86.3 Injury of muscle(s) and tendon(s) of peroneal muscle group at lower leg level	0.001	0.999	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	0.001	0.999	0.000
Q25 Congenital malformations of great arteries	0.001	0.999	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.001	0.999	0.000
Q51 Congenital malformations of uterus and cervix	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
F60.6 Anxious [avoidant] personality disorder	0.001	0.999	0.000
K04.5 Chronic apical periodontitis	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
Q99.8 Other specified chromosome abnormalities	0.001	0.999	0.000
S80.9 Superficial injury of lower leg, unspecified	0.001	0.999	0.000
S86.1 Injury of other muscle(s) and tendon(s) of posterior muscle group at lower leg level	0.001	0.999	0.000
V23.5 Passenger injured in traffic accident	0.001	0.999	0.000
V28.2 Unspecified motorcycle rider injured in nontraffic accident	0.001	0.999	0.000
H34 Retinal vascular occlusions	0.000	0.999	0.001
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
Q60 Renal agenesis and other reduction defects of kidney	0.001	0.999	0.000
D05.0 Lobular carcinoma in situ	0.001	0.999	0.000
F60.0 Paranoid personality disorder	0.001	0.999	0.000
G44.0 Cluster headache syndrome	0.000	0.999	0.001
O36.6 Maternal care for excessive foetal growth	0.001	0.999	0.000
Q43.8 Other specified congenital malformations of intestine	0.001	0.999	0.000
Q66.3 Other congenital varus deformities of feet	0.001	0.999	0.000
S86.2 Injury of muscle(s) and tendon(s) of anterior muscle group at lower leg level	0.001	0.999	0.000
Q36 Cleft lip	0.001	0.999	0.000
Q43 Other congenital malformations of intestine	0.001	0.999	0.000
M40.29 Other and unspecified kyphosis (Site unspecified)	0.001	0.999	0.000
M48.07 Spinal stenosis (Lumbosacral region)	0.000	0.999	0.001
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
Q24.6 Congenital heart block	0.001	0.999	0.000
Q31.9 Congenital malformation of larynx, unspecified	0.001	0.999	0.000
Q31.8 Other congenital malformations of larynx	0.001	0.999	0.000
Q31.5 Congenital laryngomalacia	0.001	0.999	0.000
Q31.4 Congenital laryngeal stridor	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