TreeWAS – Variant ID: rs12950363

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
C22.0 Liver cell carcinoma	0.009	0.991	0.000
C22 Malignant neoplasm of liver and intrahepatic bile ducts	0.009	0.991	0.000
T93.2 Sequelae of other fractures of lower limb	0.009	0.991	0.000
T93 Sequelae of injuries of lower limb	0.008	0.992	0.000
C22.9 Liver, unspecified	0.008	0.992	0.000
C15-C26 Malignant neoplasms of digestive organs	0.008	0.992	0.000
T93.9 Sequelae of unspecified injury of lower limb	0.008	0.992	0.000
C19 Malignant neoplasm of rectosigmoid junction	0.008	0.992	0.000
C18.9 Colon, unspecified	0.007	0.993	0.000
C18 Malignant neoplasm of colon	0.007	0.993	0.000
T93.0 Sequelae of open wound of lower limb	0.007	0.993	0.000
C23 Malignant neoplasm of gallbladder	0.007	0.993	0.000
C20 Malignant neoplasm of rectum	0.007	0.993	0.000
T93.3 Sequelae of dislocation, sprain and strain of lower limb	0.007	0.993	0.000
C25 Malignant neoplasm of pancreas	0.007	0.993	0.000
T93.1 Sequelae of fracture of femur	0.007	0.993	0.000
C22.7 Other specified carcinomas of liver	0.007	0.993	0.000
C22.4 Other sarcomas of liver	0.007	0.993	0.000
C22.3 Angiosarcoma of liver	0.007	0.993	0.000
C22.2 Hepatoblastoma	0.007	0.993	0.000
C17 Malignant neoplasm of small intestine	0.007	0.993	0.000
R93.2 Abnormal findings on diagnostic imaging of liver and biliary tract	0.000	0.993	0.007
T93.5 Sequelae of injury of muscle and tendon of lower limb	0.006	0.993	0.000
C18.6 Descending colon	0.006	0.994	0.000
T93.8 Sequelae of other specified injuries of lower limb	0.006	0.994	0.000
T93.6 Sequelae of crushing injury and traumatic amputation of lower limb	0.006	0.994	0.000
T93.4 Sequelae of injury of nerve of lower limb	0.006	0.994	0.000
C16 Malignant neoplasm of stomach	0.006	0.994	0.000
C24 Malignant neoplasm of other and unspecified parts of biliary tract	0.006	0.994	0.000
C22.1 Intrahepatic bile duct carcinoma	0.006	0.994	0.000
C25.0 Head of pancreas	0.006	0.994	0.000
C26 Malignant neoplasm of other and ill-defined digestive organs	0.006	0.994	0.000
C18.7 Sigmoid colon	0.006	0.994	0.000
C18.0 Caecum	0.006	0.994	0.000
C25.9 Pancreas, unspecified	0.006	0.994	0.000
C17.0 Duodenum	0.006	0.994	0.000
C16.3 Pyloric antrum	0.006	0.994	0.000
C18.1 Appendix	0.006	0.994	0.000
C16.5 Lesser curvature of stomach, unspecified	0.005	0.994	0.000
C18.8 Overlapping lesion of colon	0.005	0.994	0.000
C18.4 Transverse colon	0.005	0.995	0.000
K02.9 Dental caries, unspecified	0.000	0.995	0.005
C25.8 Overlapping lesion of pancreas	0.005	0.995	0.000
C25.7 Other parts of pancreas	0.005	0.995	0.000
C25.4 Endocrine pancreas	0.005	0.995	0.000
C25.3 Pancreatic duct	0.005	0.995	0.000
C25.1 Body of pancreas	0.005	0.995	0.000
C17.9 Small intestine, unspecified	0.005	0.995	0.000
C17.8 Overlapping lesion of small intestine	0.005	0.995	0.000
C17.3 Meckel's diverticulum	0.005	0.995	0.000
C17.2 Ileum	0.005	0.995	0.000
C17.1 Jejunum	0.005	0.995	0.000
C24.1 Ampulla of Vater	0.005	0.995	0.000
R93.4 Abnormal findings on diagnostic imaging of urinary organs	0.000	0.995	0.005
R93 Abnormal findings on diagnostic imaging of other body structures	0.000	0.995	0.005
C21 Malignant neoplasm of anus and anal canal	0.005	0.995	0.000
C16.8 Overlapping lesion of stomach	0.005	0.995	0.000
C16.6 Greater curvature of stomach, unspecified	0.005	0.995	0.000
C16.4 Pylorus	0.005	0.995	0.000
C16.2 Body of stomach	0.005	0.995	0.000
C16.1 Fundus of stomach	0.005	0.995	0.000
C24.9 Biliary tract, unspecified	0.005	0.995	0.000
C24.8 Overlapping lesion of biliary tract	0.005	0.995	0.000
C26.9 Ill-defined sites within the digestive system	0.005	0.995	0.000
D86.9 Sarcoidosis, unspecified	0.005	0.995	0.000
C25.2 Tail of pancreas	0.005	0.995	0.000
C18.5 Splenic flexure	0.005	0.995	0.000
C18.2 Ascending colon	0.005	0.995	0.000
D13.1 Stomach	0.005	0.995	0.000
R93.0 Abnormal findings on diagnostic imaging of skull and head, not elsewhere classified	0.000	0.995	0.005
C24.0 Extrahepatic bile duct	0.004	0.995	0.000
C26.8 Overlapping lesion of digestive system	0.004	0.995	0.000
C26.1 Spleen	0.004	0.995	0.000
E05.0 Thyrotoxicosis with diffuse goitre	0.004	0.996	0.000
R93.5 Abnormal findings on diagnostic imaging of other abdominal regions, including retroperitoneum	0.000	0.996	0.004
C18.3 Hepatic flexure	0.004	0.996	0.000
D50.9 Iron deficiency anaemia, unspecified	0.004	0.996	0.000
C16.0 Cardia	0.004	0.996	0.000
R93.1 Abnormal findings on diagnostic imaging of heart and coronary circulation	0.000	0.996	0.004
R93.7 Abnormal findings on diagnostic imaging of other parts of musculoskeletal system	0.000	0.996	0.004
Z47.0 Follow-up care involving removal of fracture plate and other internal fixation device	0.004	0.996	0.000
C26.0 Intestinal tract, part unspecified	0.004	0.996	0.000
R93.6 Abnormal findings on diagnostic imaging of limbs	0.000	0.996	0.004
D86 Sarcoidosis	0.004	0.996	0.000
C21.8 Overlapping lesion of rectum, anus and anal canal	0.004	0.996	0.000
C21.2 Cloacogenic zone	0.004	0.996	0.000
S82.60 Fracture of lateral malleolus (closed)	0.000	0.996	0.004
Z01.8 Other specified special examinations	0.000	0.997	0.003
H81.0 Meniere's disease	0.000	0.997	0.003
D86.0 Sarcoidosis of lung	0.003	0.997	0.000
C21.1 Anal canal	0.003	0.997	0.000
K20 Oesophagitis	0.003	0.997	0.000
C85.1 B-cell lymphoma, unspecified	0.003	0.997	0.000
C21.0 Anus, unspecified	0.003	0.997	0.000
D86.8 Sarcoidosis of other and combined sites	0.003	0.997	0.000
C64 Malignant neoplasm of kidney, except renal pelvis	0.000	0.997	0.003
D86.3 Sarcoidosis of skin	0.003	0.997	0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.003	0.997	0.000
R93.8 Abnormal findings on diagnostic imaging of other specified body structures	0.000	0.997	0.003
C16.9 Stomach, unspecified	0.003	0.997	0.000
Z36.0 Antenatal screening for chromosomal anomalies	0.000	0.997	0.003
D80-D89 Certain disorders involving the immune mechanism	0.003	0.997	0.000
H11.3 Conjunctival haemorrhage	0.003	0.997	0.000
R61.9 Hyperhidrosis, unspecified	0.003	0.997	0.000
D13 Benign neoplasm of other and ill-defined parts of digestive system	0.003	0.997	0.000
D86.1 Sarcoidosis of lymph nodes	0.003	0.997	0.000
Q61.3 Polycystic kidney, unspecified	0.000	0.997	0.003
D70 Agranulocytosis	0.003	0.997	0.000
K62.8 Other specified diseases of anus and rectum	0.003	0.997	0.000
D73.0 Hyposplenism	0.003	0.997	0.000
M23.24 Derangement of meniscus due to old tear or injury (Lateral collateral ligament or Anterior horn of lateral meniscus)	0.003	0.997	0.000
D13.2 Duodenum	0.003	0.997	0.000
T42.4 Benzodiazepines	0.003	0.997	0.000
D73 Diseases of spleen	0.003	0.997	0.000
Z36.8 Other antenatal screening	0.000	0.997	0.003
Z88.3 Personal history of allergy to other anti-infective agents	0.003	0.997	0.000
M22.8 Other disorders of patella	0.003	0.997	0.000
D80 Immunodeficiency with predominantly antibody defects	0.002	0.997	0.000
D70-D77 Other diseases of blood and blood-forming organs	0.002	0.997	0.000
Q61.2 Polycystic kidney, adult type	0.000	0.998	0.002
C15 Malignant neoplasm of oesophagus	0.002	0.998	0.000
D84 Other immunodeficiencies	0.002	0.998	0.000
K02 Dental caries	0.000	0.998	0.002
D58 Other hereditary haemolytic anaemias	0.002	0.998	0.000
Q61 Cystic kidney disease	0.000	0.998	0.002
D13.5 Extrahepatic bile ducts	0.002	0.998	0.000
O47.1 False labour at or after 37 completed weeks of gestation	0.000	0.998	0.002
Z36 Antenatal screening	0.000	0.998	0.002
D55-D59 Haemolytic anaemias	0.002	0.998	0.000
D83 Common variable immunodeficiency	0.002	0.998	0.000
D82 Immunodeficiency associated with other major defects	0.002	0.998	0.000
D81 Combined immunodeficiencies	0.002	0.998	0.000
D13.9 Ill-defined sites within the digestive system	0.002	0.998	0.000
D13.7 Endocrine pancreas	0.002	0.998	0.000
D13.6 Pancreas	0.002	0.998	0.000
D13.4 Liver	0.002	0.998	0.000
D13.3 Other and unspecified parts of small intestine	0.002	0.998	0.000
D13.0 Oesophagus	0.002	0.998	0.000
D58.9 Hereditary haemolytic anaemia, unspecified	0.002	0.998	0.000
D59 Acquired haemolytic anaemia	0.002	0.998	0.000
D59.1 Other autoimmune haemolytic anaemias	0.002	0.998	0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.002	0.998	0.000
D73.8 Other diseases of spleen	0.002	0.998	0.000
R93.3 Abnormal findings on diagnostic imaging of other parts of digestive tract	0.000	0.998	0.002
D58.0 Hereditary spherocytosis	0.002	0.998	0.000
D73.9 Disease of spleen, unspecified	0.002	0.998	0.000
D73.4 Cyst of spleen	0.002	0.998	0.000
D73.3 Abscess of spleen	0.002	0.998	0.000
D73.2 Chronic congestive splenomegaly	0.002	0.998	0.000
D73.1 Hypersplenism	0.002	0.998	0.000
H11.4 Other conjunctival vascular disorders and cysts	0.002	0.998	0.000
Z36.2 Other antenatal screening based on amniocentesis	0.000	0.998	0.002
H81 Disorders of vestibular function	0.000	0.998	0.002
D73.5 Infarction of spleen	0.002	0.998	0.000
D84.9 Immunodeficiency, unspecified	0.002	0.998	0.000
D80.1 Nonfamilial hypogammaglobulinaemia	0.002	0.998	0.000
D50 Iron deficiency anaemia	0.002	0.998	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.002	0.998	0.000
D80.8 Other immunodeficiencies with predominantly antibody defects	0.002	0.998	0.000
D80.7 Transient hypogammaglobulinaemia of infancy	0.002	0.998	0.000
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.002	0.998	0.000
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.002	0.998	0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.002	0.998	0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.002	0.998	0.000
D80.0 Hereditary hypogammaglobulinaemia	0.002	0.998	0.000
F20.9 Schizophrenia, unspecified	0.000	0.998	0.002
O47.0 False labour before 37 completed weeks of gestation	0.000	0.998	0.002
Z36.4 Antenatal screening for foetal growth retardation using ultrasound and other physical methods	0.000	0.998	0.002
D74 Methaemoglobinaemia	0.002	0.998	0.000
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere	0.002	0.998	0.000
D71 Functional disorders of polymorphonuclear neutrophils	0.002	0.998	0.000
H11 Other disorders of conjunctiva	0.002	0.998	0.000
M85.89 Other specified disorders of bone density and structure (Site unspecified)	0.002	0.998	0.000
H81.1 Benign paroxysmal vertigo	0.000	0.998	0.002
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.002	0.998	0.000
C15.8 Overlapping lesion of oesophagus	0.002	0.998	0.000
C15.3 Upper third of oesophagus	0.002	0.998	0.000
C15.2 Abdominal part of oesophagus	0.002	0.998	0.000
C15.1 Thoracic part of oesophagus	0.002	0.998	0.000
C15.0 Cervical part of oesophagus	0.002	0.998	0.000
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.002	0.998	0.000
D84.8 Other specified immunodeficiencies	0.002	0.998	0.000
D84.1 Defects in the complement system	0.002	0.998	0.000
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.002	0.998	0.000
F20.0 Paranoid schizophrenia	0.000	0.998	0.002
K02.5 Caries with pulp exposure	0.000	0.998	0.002
K02.4 Odontoclasia	0.000	0.998	0.002
K02.3 Arrested dental caries	0.000	0.998	0.002
K02.2 Caries of cementum	0.000	0.998	0.002
K02.1 Caries of dentin	0.000	0.998	0.002
K02.0 Caries limited to enamel	0.000	0.998	0.002
Q61.9 Cystic kidney disease, unspecified	0.000	0.998	0.002
Q61.8 Other cystic kidney diseases	0.000	0.998	0.002
Q61.5 Medullary cystic kidney	0.000	0.998	0.002
Q61.4 Renal dysplasia	0.000	0.998	0.002
Q61.1 Polycystic kidney, infantile type	0.000	0.998	0.002
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.002	0.998	0.000
D58.8 Other specified hereditary haemolytic anaemias	0.002	0.998	0.000
D58.2 Other haemoglobinopathies	0.002	0.998	0.000
D58.1 Hereditary elliptocytosis	0.002	0.998	0.000
H11.8 Other specified disorders of conjunctiva	0.002	0.998	0.000
K02.8 Other dental caries	0.000	0.998	0.002
S32.50 Fracture of pubis (closed)	0.002	0.998	0.000
D81.9 Combined immunodeficiency, unspecified	0.002	0.998	0.000
D81.8 Other combined immunodeficiencies	0.002	0.998	0.000
D81.7 Major histocompatibility complex class II deficiency	0.002	0.998	0.000
D81.6 Major histocompatibility complex class I deficiency	0.002	0.998	0.000
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.002	0.998	0.000
D81.4 Nezelof's syndrome	0.002	0.998	0.000
D81.3 Adenosine deaminase [ADA] deficiency	0.002	0.998	0.000
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.002	0.998	0.000
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.002	0.998	0.000
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.002	0.998	0.000
D82.9 Immunodeficiency associated with major defect, unspecified	0.002	0.998	0.000
D82.8 Immunodeficiency associated with other specified major defects	0.002	0.998	0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.002	0.998	0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.002	0.998	0.000
D82.2 Immunodeficiency with short-limbed stature	0.002	0.998	0.000
D82.1 Di George's syndrome	0.002	0.998	0.000
D82.0 Wiskott-Aldrich syndrome	0.002	0.998	0.000
D83.9 Common variable immunodeficiency, unspecified	0.002	0.998	0.000
D83.8 Other common variable immunodeficiencies	0.002	0.998	0.000
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells	0.002	0.998	0.000
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders	0.002	0.998	0.000
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function	0.002	0.998	0.000
R19.8 Other specified symptoms and signs involving the digestive system and abdomen	0.000	0.998	0.002
T42.6 Other antiepileptic and sedative-hypnotic drugs	0.002	0.998	0.000
Z36.9 Antenatal screening, unspecified	0.000	0.998	0.002
Z36.5 Antenatal screening for isoimmunisation	0.000	0.998	0.002
Z36.3 Antenatal screening for malformations using ultrasound and other physical methods	0.000	0.998	0.002
D57 Sickle-cell disorders	0.002	0.998	0.000
D56 Thalassaemia	0.002	0.998	0.000
D55 Anaemia due to enzyme disorders	0.002	0.998	0.000
I77.6 Arteritis, unspecified	0.000	0.998	0.002
M23.20 Derangement of meniscus due to old tear or injury (Multiple sites)	0.002	0.998	0.000
Q61.0 Congenital single renal cyst	0.000	0.998	0.002
M89.87 Other specified disorders of bone (Ankle and foot)	0.002	0.998	0.000
D59.9 Acquired haemolytic anaemia, unspecified	0.002	0.998	0.000
D59.8 Other acquired haemolytic anaemias	0.002	0.998	0.000
D59.6 Haemoglobinuria due to haemolysis from other external causes	0.002	0.998	0.000
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]	0.002	0.998	0.000
D59.4 Other nonautoimmune haemolytic anaemias	0.002	0.998	0.000
D59.3 Haemolytic-uraemic syndrome	0.002	0.998	0.000
D59.2 Drug-induced nonautoimmune haemolytic anaemia	0.002	0.998	0.000
D59.0 Drug-induced autoimmune haemolytic anaemia	0.002	0.998	0.000
I77.8 Other specified disorders of arteries and arterioles	0.000	0.998	0.002
H81.2 Vestibular neuronitis	0.000	0.998	0.002
N41.0 Acute prostatitis	0.000	0.998	0.002
Z87.8 Personal history of other specified conditions	0.002	0.998	0.000
T42 Poisoning by antiepileptic, sedative-hypnotic and anti-Parkinsonism drugs	0.002	0.998	0.000
F20 Schizophrenia	0.000	0.998	0.002
O47 False labour	0.000	0.998	0.002
D50-D53 Nutritional anaemias	0.002	0.998	0.000
E10.4 With neurological complications	0.002	0.998	0.000
S82.6 Fracture of lateral malleolus	0.000	0.998	0.002
H81.8 Other disorders of vestibular function	0.000	0.998	0.002
H81.4 Vertigo of central origin	0.000	0.998	0.002
H81.3 Other peripheral vertigo	0.000	0.998	0.002
D75 Other diseases of blood and blood-forming organs	0.002	0.998	0.000
D72 Other disorders of white blood cells	0.002	0.998	0.000
C15.4 Middle third of oesophagus	0.001	0.998	0.000
D50.1 Sideropenic dysphagia	0.002	0.998	0.000
I77 Other disorders of arteries and arterioles	0.000	0.998	0.002
D05.1 Intraductal carcinoma in situ	0.000	0.998	0.002
Q63.0 Accessory kidney	0.002	0.998	0.000
M23.21 Derangement of meniscus due to old tear or injury (Anterior cruciate ligament or Anterior horn of medial meniscus)	0.002	0.998	0.000
M65.96 Synovitis and tenosynovitis, unspecified (Lower leg)	0.000	0.998	0.002
D74.9 Methaemoglobinaemia, unspecified	0.002	0.998	0.000
D74.8 Other methaemoglobinaemias	0.002	0.998	0.000
D74.0 Congenital methaemoglobinaemia	0.002	0.998	0.000
H11.2 Conjunctival scars	0.002	0.998	0.000
I77.1 Stricture of artery	0.000	0.998	0.002
Z36.1 Antenatal screening for raised alphafetoprotein level	0.000	0.998	0.002
D76.2 Haemophagocytic syndrome, infection-associated	0.002	0.998	0.000
D76.1 Haemophagocytic lymphohistiocytosis	0.002	0.998	0.000
D76.0 Langerhans' cell histiocytosis, not elsewhere classified	0.002	0.998	0.000
M22.2 Patellofemoral disorders	0.002	0.998	0.000
I77.9 Disorder of arteries and arterioles, unspecified	0.000	0.998	0.002
M79.29 Neuralgia and neuritis, unspecified (Site unspecified)	0.002	0.998	0.000
C71.9 Brain, unspecified	0.000	0.998	0.002
D75.0 Familial erythrocytosis	0.002	0.998	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.001	0.998	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.001	0.998	0.000
D89.3 Immune reconstitution syndrome	0.001	0.998	0.000
D89.1 Cryoglobulinaemia	0.001	0.998	0.000
D89.0 Polyclonal hypergammaglobulinaemia	0.001	0.998	0.000
H11.9 Disorder of conjunctiva, unspecified	0.002	0.998	0.000
O36.0 Maternal care for rhesus isoimmunisation	0.000	0.998	0.002
H40.9 Glaucoma, unspecified	0.000	0.998	0.002
M23.99 Internal derangement of knee, unspecified (Unspecified ligament or Unspecified meniscus)	0.002	0.998	0.000
D55.9 Anaemia due to enzyme disorder, unspecified	0.001	0.998	0.000
D55.8 Other anaemias due to enzyme disorders	0.001	0.998	0.000
D55.3 Anaemia due to disorders of nucleotide metabolism	0.001	0.998	0.000
D55.2 Anaemia due to disorders of glycolytic enzymes	0.001	0.998	0.000
D55.1 Anaemia due to other disorders of glutathione metabolism	0.001	0.998	0.000
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency	0.001	0.998	0.000
D56.9 Thalassaemia, unspecified	0.001	0.998	0.000
D56.8 Other thalassaemias	0.001	0.998	0.000
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]	0.001	0.998	0.000
D56.3 Thalassaemia trait	0.001	0.998	0.000
D56.2 Delta-beta thalassaemia	0.001	0.998	0.000
D56.1 Beta thalassaemia	0.001	0.998	0.000
D56.0 Alpha thalassaemia	0.001	0.998	0.000
D57.8 Other sickle-cell disorders	0.001	0.998	0.000
D57.3 Sickle-cell trait	0.001	0.998	0.000
D57.2 Double heterozygous sickling disorders	0.001	0.998	0.000
D57.1 Sickle-cell anaemia without crisis	0.001	0.998	0.000
D57.0 Sickle-cell anaemia with crisis	0.001	0.998	0.000
D76.3 Other histiocytosis syndromes	0.001	0.998	0.000
N18.3 Chronic kidney disease, stage 3	0.000	0.998	0.002
H81.9 Disorder of vestibular function, unspecified	0.000	0.998	0.001
I46.0 Cardiac arrest with successful resuscitation	0.002	0.998	0.000
M23.2 Derangement of meniscus due to old tear or injury	0.002	0.998	0.000
E05 Thyrotoxicosis [hyperthyroidism]	0.002	0.998	0.000
E10.1 With ketoacidosis	0.002	0.998	0.000
H11.1 Conjunctival degenerations and deposits	0.002	0.998	0.000
U89.8 Agent resistant to other single specified antibiotic	0.002	0.998	0.000
B18.2 Chronic viral hepatitis C	0.002	0.998	0.000
E10.5 With peripheral circulatory complications	0.002	0.998	0.000
Q60.0 Renal agenesis, unilateral	0.001	0.998	0.000
Q65.8 Other congenital deformities of hip	0.002	0.998	0.000
Z00.6 Examination for normal comparison and control in clinical research programme	0.002	0.998	0.000
Z47 Other orthopaedic follow-up care	0.002	0.998	0.000
T90-T98 Sequelae of injuries, of poisoning and of other consequences of external causes	0.002	0.998	0.000
Q60-Q64 Congenital malformations of the urinary system	0.001	0.998	0.000
M48.07 Spinal stenosis (Lumbosacral region)	0.002	0.998	0.000
Q50.4 Embryonic cyst of Fallopian tube	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.001	0.998	0.000
S22.00 Fracture of thoracic vertebra (closed)	0.000	0.998	0.002
D72.1 Eosinophilia	0.001	0.998	0.000
T42.8 Anti-Parkinsonism drugs and other central muscle-tone depressants	0.001	0.998	0.000
T42.7 Antiepileptic and sedative-hypnotic drugs, unspecified	0.001	0.998	0.000
T42.5 Mixed antiepileptics, not elsewhere classified	0.001	0.998	0.000
T42.3 Barbiturates	0.001	0.998	0.000
T42.2 Succinimides and oxazolidinediones	0.001	0.998	0.000
T42.1 Iminostilbenes	0.001	0.998	0.000
T42.0 Hydantoin derivatives	0.001	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.001	0.998	0.000
C32.0 Glottis	0.002	0.998	0.000
F20.8 Other schizophrenia	0.000	0.998	0.001
F20.6 Simple schizophrenia	0.000	0.998	0.001
F20.5 Residual schizophrenia	0.000	0.998	0.001
F20.4 Postschizophrenic depression	0.000	0.998	0.001
F20.3 Undifferentiated schizophrenia	0.000	0.998	0.001
F20.2 Catatonic schizophrenia	0.000	0.998	0.001
F20.1 Hebephrenic schizophrenia	0.000	0.998	0.001
O47.9 False labour, unspecified	0.000	0.998	0.002
Q65 Congenital deformities of hip	0.001	0.998	0.000
S82.61 Fracture of lateral malleolus (open)	0.000	0.998	0.001
C71.1 Frontal lobe	0.000	0.998	0.002
D72.9 Disorder of white blood cells, unspecified	0.001	0.998	0.000
D72.0 Genetic anomalies of leukocytes	0.001	0.998	0.000
K63.3 Ulcer of intestine	0.000	0.998	0.002
N41.9 Inflammatory disease of prostate, unspecified	0.000	0.998	0.002
Q66.8 Other congenital deformities of feet	0.001	0.998	0.000
Y42.8 Other and unspecified hormones and their synthetic substitutes	0.002	0.998	0.000
Z47.9 Orthopaedic follow-up care, unspecified	0.001	0.998	0.000
Q66 Congenital deformities of feet	0.001	0.998	0.000
M79.66 Pain in limb (Lower leg)	0.002	0.998	0.000
C71.2 Temporal lobe	0.000	0.998	0.002
I77.5 Necrosis of artery	0.000	0.998	0.001
I77.4 Coeliac artery compression syndrome	0.000	0.998	0.001
I77.3 Arterial fibromuscular dysplasia	0.000	0.998	0.001
I77.2 Rupture of artery	0.000	0.998	0.001
I77.0 Arteriovenous fistula, acquired	0.000	0.998	0.001
I95.2 Hypotension due to drugs	0.002	0.998	0.000
D75.9 Disease of blood and blood-forming organs, unspecified	0.001	0.998	0.000
D75.2 Essential thrombocytosis	0.001	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)	0.001	0.998	0.000
D53 Other nutritional anaemias	0.001	0.998	0.000
Q64 Other congenital malformations of urinary system	0.001	0.998	0.000
H11.0 Pterygium	0.001	0.998	0.000
M89.8 Other specified disorders of bone	0.001	0.998	0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.001	0.998	0.000
R61 Hyperhidrosis	0.001	0.998	0.000
M23.27 Derangement of meniscus due to old tear or injury-Capsular	0.001	0.999	0.000
M41.96 Scoliosis, unspecified (Lumbar region)	0.000	0.999	0.001
M89.84 Other specified disorders of bone (Hand)	0.001	0.999	0.000
R61.0 Localised hyperhidrosis	0.001	0.999	0.000
S63.6 Sprain and strain of finger(s)	0.001	0.999	0.000
Z99.2 Dependence on renal dialysis	0.000	0.999	0.001
C71 Malignant neoplasm of brain	0.000	0.999	0.001
E05.8 Other thyrotoxicosis	0.001	0.999	0.000
E05.5 Thyroid crisis or storm	0.001	0.999	0.000
E05.4 Thyrotoxicosis factitia	0.001	0.999	0.000
E05.3 Thyrotoxicosis from ectopic thyroid tissue	0.001	0.999	0.000
E05.1 Thyrotoxicosis with toxic single thyroid nodule	0.001	0.999	0.000
M22 Disorders of patella	0.001	0.999	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.001	0.999	0.000
T94 Sequelae of injuries involving multiple and unspecified body regions	0.001	0.999	0.000
I50.0 Congestive heart failure	0.001	0.999	0.000
M85.8 Other specified disorders of bone density and structure	0.001	0.999	0.000
Q66.3 Other congenital varus deformities of feet	0.001	0.999	0.000
Q85.0 Neurofibromatosis (nonmalignant)	0.001	0.999	0.000
D52 Folate deficiency anaemia	0.001	0.999	0.000
D66 Hereditary factor VIII deficiency	0.001	0.999	0.000
E10 Insulin-dependent diabetes mellitus	0.001	0.999	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.001	0.999	0.000
T95 Sequelae of burns, corrosions and frostbite	0.001	0.999	0.000
T97 Sequelae of toxic effects of substances chiefly nonmedicinal as to source	0.001	0.999	0.000
T96 Sequelae of poisoning by drugs, medicaments and biological substances	0.001	0.999	0.000
M89.85 Other specified disorders of bone (Pelvic region and thigh)	0.001	0.999	0.000
H40.5 Glaucoma secondary to other eye disorders	0.000	0.999	0.001
Q60.6 Potter's syndrome	0.001	0.999	0.000
Q60.5 Renal hypoplasia, unspecified	0.001	0.999	0.000
Q60.4 Renal hypoplasia, bilateral	0.001	0.999	0.000
Q60.3 Renal hypoplasia, unilateral	0.001	0.999	0.000
Q60.2 Renal agenesis, unspecified	0.001	0.999	0.000
Q60.1 Renal agenesis, bilateral	0.001	0.999	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.001	0.999	0.000
Q63.8 Other specified congenital malformations of kidney	0.001	0.999	0.000
Q63.3 Hyperplastic and giant kidney	0.001	0.999	0.000
Q63.2 Ectopic kidney	0.001	0.999	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.001	0.999	0.000
Q65.9 Congenital deformity of hip, unspecified	0.001	0.999	0.000
Q65.6 Unstable hip	0.001	0.999	0.000
Q65.5 Congenital subluxation of hip, unspecified	0.001	0.999	0.000
Q65.4 Congenital subluxation of hip, bilateral	0.001	0.999	0.000
Q65.3 Congenital subluxation of hip, unilateral	0.001	0.999	0.000
Q65.2 Congenital dislocation of hip, unspecified	0.001	0.999	0.000
Q65.1 Congenital dislocation of hip, bilateral	0.001	0.999	0.000
Q65.0 Congenital dislocation of hip, unilateral	0.001	0.999	0.000
G35 Multiple sclerosis	0.001	0.999	0.000
E05.2 Thyrotoxicosis with toxic multinodular goitre	0.001	0.999	0.000
E10.3 With ophthalmic complications	0.001	0.999	0.000
H40.1 Primary open-angle glaucoma	0.000	0.999	0.001
M23.9 Internal derangement of knee, unspecified	0.001	0.999	0.000
Q21.0 Ventricular septal defect	0.001	0.999	0.000
Q66.9 Congenital deformity of feet, unspecified	0.001	0.999	0.000
Q66.7 Pes cavus	0.001	0.999	0.000
Q66.6 Other congenital valgus deformities of feet	0.001	0.999	0.000
Q66.5 Congenital pes planus	0.001	0.999	0.000
Q66.4 Talipes calcaneovalgus	0.001	0.999	0.000
Q66.2 Metatarsus varus	0.001	0.999	0.000
Q66.1 Talipes calcaneovarus	0.001	0.999	0.000
Q66.0 Talipes equinovarus	0.001	0.999	0.000
Z01.7 Laboratory examination	0.000	0.999	0.001
Q76 Congenital malformations of spine and bony thorax	0.001	0.999	0.000
D75.8 Other specified diseases of blood and blood-forming organs	0.001	0.999	0.000
E10.0 With coma	0.001	0.999	0.000
E80.4 Gilbert's syndrome	0.001	0.999	0.000
M22.0 Recurrent dislocation of patella	0.001	0.999	0.000
Q67.5 Congenital deformity of spine	0.001	0.999	0.000
V49.4 Driver injured in collision with other and unspecified motor vehicles in traffic accident	0.001	0.999	0.000
Q78 Other osteochondrodysplasias	0.001	0.999	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.001	0.999	0.000
Q75 Other congenital malformations of skull and face bones	0.001	0.999	0.000
Q74 Other congenital malformations of limb(s)	0.001	0.999	0.000
Q73 Reduction defects of unspecified limb	0.001	0.999	0.000
Q72 Reduction defects of lower limb	0.001	0.999	0.000
Q71 Reduction defects of upper limb	0.001	0.999	0.000
Q70 Syndactyly	0.001	0.999	0.000
Q69 Polydactyly	0.001	0.999	0.000
Q68 Other congenital musculoskeletal deformities	0.001	0.999	0.000
Q50-Q56 Congenital malformations of genital organs	0.001	0.999	0.000
M23.80 Other internal derangements of knee (Multiple sites)	0.001	0.999	0.000
D53.8 Other specified nutritional anaemias	0.001	0.999	0.000
D53.2 Scorbutic anaemia	0.001	0.999	0.000
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.001	0.999	0.000
D53.0 Protein deficiency anaemia	0.001	0.999	0.000
M23.8 Other internal derangements of knee	0.001	0.999	0.000
O42.1 Premature rupture of membranes, onset of labour after 24 hours	0.000	0.999	0.001
Q24.8 Other specified congenital malformations of heart	0.001	0.999	0.000
T98 Sequelae of other and unspecified effects of external causes	0.001	0.999	0.000
M89.89 Other specified disorders of bone (Site unspecified)	0.001	0.999	0.000
M89.88 Other specified disorders of bone (Other)	0.001	0.999	0.000
M89.83 Other specified disorders of bone (Forearm)	0.001	0.999	0.000
M89.82 Other specified disorders of bone (Upper arm)	0.001	0.999	0.000
M89.81 Other specified disorders of bone (Shoulder region)	0.001	0.999	0.000
M89.80 Other specified disorders of bone (Multiple sites)	0.001	0.999	0.000
C71.3 Parietal lobe	0.000	0.999	0.001
L02.2 Cutaneous abscess, furuncle and carbuncle of trunk	0.000	0.999	0.001
Q50.6 Other congenital malformatons of Fallopian tube and broad ligament	0.001	0.999	0.000
Q50.5 Embryonic cyst of broad ligament	0.001	0.999	0.000
Q50.3 Other congenital malformations of ovary	0.001	0.999	0.000
Q50.2 Congenital torsion of ovary	0.001	0.999	0.000
Q50.1 Developmental ovarian cyst	0.001	0.999	0.000
Q50.0 Congenital absence of ovary	0.001	0.999	0.000
Q62.5 Duplication of ureter	0.001	0.999	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.001	0.999	0.000
Q64.8 Other specified congenital malformations of urinary system	0.001	0.999	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.001	0.999	0.000
Q64.6 Congenital diverticulum of bladder	0.001	0.999	0.000
Q64.5 Congenital absence of bladder and urethra	0.001	0.999	0.000
Q64.4 Malformation of urachus	0.001	0.999	0.000
Q64.2 Congenital posterior urethral valves	0.001	0.999	0.000
Q64.1 Exstrophy of urinary bladder	0.001	0.999	0.000
Q64.0 Epispadias	0.001	0.999	0.000
Q76.0 Spina bifida occulta	0.001	0.999	0.000
N41 Inflammatory diseases of prostate	0.000	0.999	0.001
Q53 Undescended testicle	0.001	0.999	0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.001	0.999	0.000
M23.25 Derangement of meniscus due to old tear or injury (Posterior horn of lateral meniscus)	0.001	0.999	0.000
M89.86 Other specified disorders of bone (Lower leg)	0.001	0.999	0.000
C71.8 Overlapping lesion of brain	0.000	0.999	0.001
C71.7 Brain stem	0.000	0.999	0.001
C71.6 Cerebellum	0.000	0.999	0.001
C71.5 Cerebral ventricle	0.000	0.999	0.001
C71.4 Occipital lobe	0.000	0.999	0.001

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