TreeWAS – Variant ID: rs17100498

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
R13 Dysphagia	0.000	0.960	0.040
D50.9 Iron deficiency anaemia, unspecified	0.000	0.979	0.021
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency	0.000	0.981	0.019
D50 Iron deficiency anaemia	0.000	0.981	0.019
D51 Vitamin B12 deficiency anaemia	0.000	0.983	0.017
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)	0.000	0.983	0.017
D50-D53 Nutritional anaemias	0.000	0.983	0.017
D50.1 Sideropenic dysphagia	0.000	0.986	0.014
D52 Folate deficiency anaemia	0.000	0.987	0.013
D51.8 Other vitamin B12 deficiency anaemias	0.000	0.987	0.013
D51.3 Other dietary vitamin B12 deficiency anaemia	0.000	0.987	0.013
D51.2 Transcobalamin II deficiency	0.000	0.987	0.013
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria	0.000	0.987	0.013
D51.9 Vitamin B12 deficiency anaemia, unspecified	0.000	0.988	0.012
K63.8 Other specified diseases of intestine	0.000	0.988	0.012
D53 Other nutritional anaemias	0.000	0.988	0.012
K63 Other diseases of intestine	0.000	0.988	0.012
K63.1 Perforation of intestine (nontraumatic)	0.000	0.989	0.011
K63.2 Fistula of intestine	0.000	0.989	0.011
K63.5 Polyp of colon	0.000	0.990	0.010
D52.9 Folate deficiency anaemia, unspecified	0.000	0.990	0.010
K63.3 Ulcer of intestine	0.000	0.990	0.010
K63.0 Abscess of intestine	0.000	0.990	0.010
D52.8 Other folate deficiency anaemias	0.000	0.990	0.009
D52.1 Drug-induced folate deficiency anaemia	0.000	0.990	0.009
D52.0 Dietary folate deficiency anaemia	0.000	0.990	0.009
D53.9 Nutritional anaemia, unspecified	0.000	0.991	0.009
D53.8 Other specified nutritional anaemias	0.000	0.991	0.009
D53.2 Scorbutic anaemia	0.000	0.991	0.009
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.000	0.991	0.009
D53.0 Protein deficiency anaemia	0.000	0.991	0.009
K63.4 Enteroptosis	0.000	0.991	0.009
K63.9 Disease of intestine, unspecified	0.000	0.991	0.009
K86.9 Disease of pancreas, unspecified	0.008	0.992	0.000
H60.9 Otitis externa, unspecified	0.008	0.992	0.000
H60 Otitis externa	0.007	0.993	0.000
K83.0 Cholangitis	0.007	0.993	0.000
K83.8 Other specified diseases of biliary tract	0.007	0.993	0.000
K83 Other diseases of biliary tract	0.007	0.993	0.000
K86 Other diseases of pancreas	0.006	0.994	0.000
H60.5 Acute otitis externa, non-infective	0.006	0.994	0.000
H61 Other disorders of external ear	0.006	0.994	0.000
H60.4 Cholesteatoma of external ear	0.006	0.994	0.000
K86.8 Other specified diseases of pancreas	0.006	0.994	0.000
H60-H62 Diseases of external ear	0.006	0.994	0.000
K83.1 Obstruction of bile duct	0.005	0.995	0.000
H60.8 Other otitis externa	0.005	0.995	0.000
K82.8 Other specified diseases of gallbladder	0.005	0.995	0.000
H61.3 Acquired stenosis of external ear canal	0.005	0.995	0.000
H60.2 Malignant otitis externa	0.005	0.995	0.000
H60.0 Abscess of external ear	0.005	0.995	0.000
K86.2 Cyst of pancreas	0.005	0.995	0.000
H60.3 Other infective otitis externa	0.005	0.995	0.000
H61.0 Perichondritis of external ear	0.005	0.995	0.000
H61.9 Disorder of external ear, unspecified	0.005	0.995	0.000
I84.2 Internal haemorrhoids without complication	0.000	0.995	0.005
K83.5 Biliary cyst	0.005	0.995	0.000
K83.4 Spasm of sphincter of Oddi	0.005	0.995	0.000
K83.3 Fistula of bile duct	0.005	0.995	0.000
K83.2 Perforation of bile duct	0.005	0.995	0.000
K86.3 Pseudocyst of pancreas	0.005	0.995	0.000
K86.0 Alcohol-induced chronic pancreatitis	0.005	0.995	0.000
N18.3 Chronic kidney disease, stage 3	0.000	0.995	0.005
H60.1 Cellulitis of external ear	0.005	0.995	0.000
H61.1 Non-infective disorders of pinna	0.005	0.995	0.000
K57.3 Diverticular disease of large intestine without perforation or abscess	0.000	0.995	0.005
K83.9 Disease of biliary tract, unspecified	0.004	0.995	0.000
K86.1 Other chronic pancreatitis	0.005	0.995	0.000
D06.9 Cervix, unspecified	0.000	0.995	0.005
H54.7 Unspecified visual loss	0.000	0.996	0.004
K82 Other diseases of gallbladder	0.004	0.996	0.000
K80-K87 Disorders of gallbladder, biliary tract and pancreas	0.004	0.996	0.000
H62 Disorders of external ear in diseases classified elsewhere	0.004	0.996	0.000
D50.8 Other iron deficiency anaemias	0.000	0.996	0.004
M48.02 Spinal stenosis (Cervical region)	0.000	0.996	0.004
B95.7 Other staphylococcus as the cause of diseases classified to other chapters	0.000	0.996	0.004
H61.8 Other specified disorders of external ear	0.004	0.996	0.000
H61.2 Impacted cerumen	0.004	0.996	0.000
I47.2 Ventricular tachycardia	0.004	0.996	0.000
N41.9 Inflammatory disease of prostate, unspecified	0.000	0.996	0.004
K82.2 Perforation of gallbladder	0.004	0.996	0.000
D09.0 Bladder	0.000	0.996	0.004
H54.4 Blindness, one eye	0.000	0.996	0.004
H54 Blindness and low vision	0.000	0.996	0.004
S06.50 Traumatic subdural haemorrhage (without open intracranial wound)	0.003	0.996	0.000
D25.2 Subserosal leiomyoma of uterus	0.003	0.997	0.000
K82.0 Obstruction of gallbladder	0.003	0.997	0.000
K82.3 Fistula of gallbladder	0.003	0.997	0.000
S06.60 Traumatic subarachnoid haemorrhage (without open intracranial wound)	0.003	0.997	0.000
K87 Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere	0.003	0.997	0.000
B95.8 Unspecified staphylococcus as the cause of diseases classified to other chapters	0.000	0.997	0.003
H54.9 Unspecified visual impairment (binocular)	0.000	0.997	0.003
H62.8 Other disorders of external ear in diseases classified elsewhere	0.003	0.997	0.000
H62.4 Otitis externa in other diseases classified elsewhere	0.003	0.997	0.000
H62.3 Otitis externa in other infectious and parasitic diseases classified elsewhere	0.003	0.997	0.000
H62.2 Otitis externa in mycoses	0.003	0.997	0.000
H62.1 Otitis externa in viral diseases classified elsewhere	0.003	0.997	0.000
H62.0 Otitis externa in bacterial diseases classified elsewhere	0.003	0.997	0.000
D86.9 Sarcoidosis, unspecified	0.000	0.997	0.003
K82.9 Disease of gallbladder, unspecified	0.003	0.997	0.000
D86 Sarcoidosis	0.000	0.997	0.003
E11.3 With ophthalmic complications	0.000	0.997	0.003
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.000	0.997	0.003
D80-D89 Certain disorders involving the immune mechanism	0.000	0.997	0.003
R60.0 Localised oedema	0.000	0.997	0.003
S06.5 Traumatic subdural haemorrhage	0.003	0.997	0.000
D06 Carcinoma in situ of cervix uteri	0.000	0.997	0.003
K82.4 Cholesterolosis of gallbladder	0.003	0.997	0.000
S06.6 Traumatic subarachnoid haemorrhage	0.003	0.997	0.000
N18.9 Chronic renal failure, unspecified	0.000	0.997	0.003
H54.6 Unqualified visual loss, one eye	0.000	0.997	0.003
H54.5 Low vision, one eye	0.000	0.997	0.003
H54.3 Unqualified visual loss, both eyes	0.000	0.997	0.003
H54.2 Low vision, both eyes	0.000	0.997	0.003
H54.1 Blindness, one eye, low vision, other eye	0.000	0.997	0.003
B95.1 Streptococcus, group B, as the cause of diseases classified to other chapters	0.000	0.997	0.003
B95 Streptococcus and staphylococcus as the cause of diseases classified to other chapters	0.000	0.997	0.003
K82.1 Hydrops of gallbladder	0.003	0.997	0.000
K87.1 Disorders of pancreas in diseases classified elsewhere	0.002	0.997	0.000
K87.0 Disorders of gallbladder and biliary tract in diseases classified elsewhere	0.002	0.997	0.000
H81.0 Meniere's disease	0.003	0.997	0.000
D86.0 Sarcoidosis of lung	0.000	0.997	0.003
D86.1 Sarcoidosis of lymph nodes	0.000	0.997	0.003
Q63.0 Accessory kidney	0.003	0.997	0.000
D09 Carcinoma in situ of other and unspecified sites	0.000	0.997	0.003
D86.3 Sarcoidosis of skin	0.000	0.997	0.002
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.000	0.997	0.002
S06 Intracranial injury	0.003	0.997	0.000
H54.0 Blindness, both eyes	0.000	0.997	0.002
D80 Immunodeficiency with predominantly antibody defects	0.000	0.997	0.002
Q63 Other congenital malformations of kidney	0.002	0.997	0.000
D84 Other immunodeficiencies	0.000	0.997	0.002
D83 Common variable immunodeficiency	0.000	0.997	0.002
D82 Immunodeficiency associated with other major defects	0.000	0.997	0.002
D81 Combined immunodeficiencies	0.000	0.997	0.002
N18 Chronic renal failure	0.000	0.997	0.003
B95.2 Streptococcus, group D, as the cause of diseases classified to other chapters	0.000	0.998	0.002
D86.8 Sarcoidosis of other and combined sites	0.000	0.998	0.002
Q63.2 Ectopic kidney	0.002	0.998	0.000
S06.51 Traumatic subdural haemorrhage (with open intracranial wound)	0.002	0.998	0.000
S06.3 Focal brain injury	0.002	0.998	0.000
D06.7 Other parts of cervix	0.000	0.998	0.002
D06.1 Exocervix	0.000	0.998	0.002
D06.0 Endocervix	0.000	0.998	0.002
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.000	0.998	0.002
S06.61 Traumatic subarachnoid haemorrhage (with open intracranial wound)	0.002	0.998	0.000
Q44.6 Cystic disease of liver	0.002	0.998	0.000
S06.30 Focal brain injury (without open intracranial wound)	0.002	0.998	0.000
G11.9 Hereditary ataxia, unspecified	0.002	0.998	0.000
G51.0 Bell's palsy	0.002	0.998	0.000
D55-D59 Haemolytic anaemias	0.000	0.998	0.002
S06.9 Intracranial injury, unspecified	0.002	0.998	0.000
K85 Acute pancreatitis	0.002	0.998	0.000
S82.80 Fractures of other parts of lower leg (closed)	0.002	0.998	0.000
B95.3 Streptococcus pneumoniae as the cause of diseases classified to other chapters	0.000	0.998	0.002
D09.9 Carcinoma in situ, unspecified	0.000	0.998	0.002
D09.7 Carcinoma in situ of other specified sites	0.000	0.998	0.002
D09.3 Thyroid and other endocrine glands	0.000	0.998	0.002
D09.2 Eye	0.000	0.998	0.002
D09.1 Other and unspecified urinary organs	0.000	0.998	0.002
S06.4 Epidural haemorrhage	0.002	0.998	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
S06.7 Intracranial injury with prolonged coma	0.002	0.998	0.000
S06.1 Traumatic cerebral oedema	0.002	0.998	0.000
D80.1 Nonfamilial hypogammaglobulinaemia	0.000	0.998	0.002
Q63.9 Congenital malformation of kidney, unspecified	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.002	0.998	0.000
R63.0 Anorexia	0.002	0.998	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.000	0.998	0.002
D80.8 Other immunodeficiencies with predominantly antibody defects	0.000	0.998	0.002
D80.7 Transient hypogammaglobulinaemia of infancy	0.000	0.998	0.002
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.000	0.998	0.002
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.000	0.998	0.002
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.000	0.998	0.002
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.000	0.998	0.002
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.000	0.998	0.002
D80.0 Hereditary hypogammaglobulinaemia	0.000	0.998	0.002
D81.9 Combined immunodeficiency, unspecified	0.000	0.998	0.002
D81.8 Other combined immunodeficiencies	0.000	0.998	0.002
D81.7 Major histocompatibility complex class II deficiency	0.000	0.998	0.002
D81.6 Major histocompatibility complex class I deficiency	0.000	0.998	0.002
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.000	0.998	0.002
D81.4 Nezelof's syndrome	0.000	0.998	0.002
D81.3 Adenosine deaminase [ADA] deficiency	0.000	0.998	0.002
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.000	0.998	0.002
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.000	0.998	0.002
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.000	0.998	0.002
D82.9 Immunodeficiency associated with major defect, unspecified	0.000	0.998	0.002
D82.8 Immunodeficiency associated with other specified major defects	0.000	0.998	0.002
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.000	0.998	0.002
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.000	0.998	0.002
D82.2 Immunodeficiency with short-limbed stature	0.000	0.998	0.002
D82.1 Di George's syndrome	0.000	0.998	0.002
D82.0 Wiskott-Aldrich syndrome	0.000	0.998	0.002
D83.9 Common variable immunodeficiency, unspecified	0.000	0.998	0.002
D83.8 Other common variable immunodeficiencies	0.000	0.998	0.002
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells	0.000	0.998	0.002
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders	0.000	0.998	0.002
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function	0.000	0.998	0.002
D84.9 Immunodeficiency, unspecified	0.000	0.998	0.002
D84.8 Other specified immunodeficiencies	0.000	0.998	0.002
D84.1 Defects in the complement system	0.000	0.998	0.002
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.000	0.998	0.002
N18.1 Chronic kidney disease, stage 1	0.000	0.998	0.002
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
D62 Acute posthaemorrhagic anaemia	0.000	0.998	0.002
Q60-Q64 Congenital malformations of the urinary system	0.002	0.998	0.000
H81.3 Other peripheral vertigo	0.002	0.998	0.000
S06.31 Focal brain injury (with open intracranial wound)	0.002	0.998	0.000
Z73.9 Problem related to life-management difficulty, unspecified	0.000	0.998	0.002
H81 Disorders of vestibular function	0.002	0.998	0.000
S06.2 Diffuse brain injury	0.002	0.998	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.000	0.998	0.002
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.000	0.998	0.002
D89.3 Immune reconstitution syndrome	0.000	0.998	0.002
D89.1 Cryoglobulinaemia	0.000	0.998	0.002
D89.0 Polyclonal hypergammaglobulinaemia	0.000	0.998	0.002
S06.90 Intracranial injury, unspecified (without open intracranial wound)	0.002	0.998	0.000
N18.2 Chronic kidney disease, stage 2	0.000	0.998	0.002
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
S06.0 Concussion	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
S06.8 Other intracranial injuries	0.002	0.998	0.000
D57 Sickle-cell disorders	0.000	0.998	0.002
D56 Thalassaemia	0.000	0.998	0.002
D55 Anaemia due to enzyme disorders	0.000	0.998	0.002
Q61 Cystic kidney disease	0.002	0.998	0.000
B95.0 Streptococcus, group A, as the cause of diseases classified to other chapters	0.000	0.998	0.002
D58 Other hereditary haemolytic anaemias	0.000	0.998	0.002
S39.9 Unspecified injury of abdomen, lower back and pelvis	0.000	0.998	0.002
S06.91 Intracranial injury, unspecified (with open intracranial wound)	0.002	0.998	0.000
K85.8 Other acute pancreatitis	0.002	0.998	0.000
K85.3 Drug-induced acute pancreatitis	0.002	0.998	0.000
K85.2 Alcohol-induced acute pancreatitis	0.002	0.998	0.000
K85.0 Idiopathic acute pancreatitis	0.002	0.998	0.000
B96.4 Proteus (mirabilis)(morganii) as the cause of diseases classified to other chapters	0.000	0.998	0.002
T85.3 Mechanical complication of other ocular prosthetic devices, imnplants and grafts	0.000	0.998	0.002
M85.89 Other specified disorders of bone density and structure (Site unspecified)	0.002	0.998	0.000
S06.40 Epidural haemorrhage (without open intracranial wound)	0.002	0.998	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.000	0.998	0.002
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
N18.8 Other chronic renal failure	0.000	0.998	0.002
S06.41 Epidural haemorrhage (with open intracranial wound)	0.002	0.998	0.000
S06.11 Traumatic cerebral oedema (with open intracranial wound)	0.002	0.998	0.000
S06.10 Traumatic cerebral oedema (without open intracranial wound)	0.002	0.998	0.000
S06.71 Intracranial injury with prolonged coma (with open intracranial wound)	0.002	0.998	0.000
S06.70 Intracranial injury with prolonged coma (without open intracranial wound)	0.002	0.998	0.000
B95.5 Unspecified streptococcus as the cause of diseases classified to other chapters	0.000	0.998	0.002
Q39.4 Oesophageal web	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	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
H36.0 Diabetic retinopathy	0.000	0.998	0.002
H81.2 Vestibular neuronitis	0.002	0.998	0.000
K22.8 Other specified diseases of oesophagus	0.000	0.998	0.002
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.998	0.000
D60-D64 Aplastic and other anaemias	0.000	0.998	0.002
D59 Acquired haemolytic anaemia	0.000	0.998	0.002
M21.37 Wrist or foot drop (acquired) (Ankle and foot)	0.000	0.998	0.002
N18.4 Chronic kidney disease, stage 4	0.000	0.998	0.002
Q64 Other congenital malformations of urinary system	0.002	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.002	0.998	0.000
D00-D09 In situ neoplasms	0.000	0.998	0.002
H81.9 Disorder of vestibular function, unspecified	0.002	0.998	0.000
H81.8 Other disorders of vestibular function	0.002	0.998	0.000
H81.4 Vertigo of central origin	0.002	0.998	0.000
N18.5 Chronic kidney disease, stage 5	0.000	0.998	0.002
S06.21 Diffuse brain injury (with open intracranial wound)	0.001	0.998	0.000
Q43 Other congenital malformations of intestine	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	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
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
S06.01 Concussion (with open intracranial wound)	0.001	0.998	0.000
D55.9 Anaemia due to enzyme disorder, unspecified	0.000	0.998	0.001
D55.8 Other anaemias due to enzyme disorders	0.000	0.998	0.001
D55.3 Anaemia due to disorders of nucleotide metabolism	0.000	0.998	0.001
D55.2 Anaemia due to disorders of glycolytic enzymes	0.000	0.998	0.001
D55.1 Anaemia due to other disorders of glutathione metabolism	0.000	0.998	0.001
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency	0.000	0.998	0.001
D56.9 Thalassaemia, unspecified	0.000	0.998	0.001
D56.8 Other thalassaemias	0.000	0.998	0.001
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]	0.000	0.998	0.001
D56.3 Thalassaemia trait	0.000	0.998	0.001
D56.2 Delta-beta thalassaemia	0.000	0.998	0.001
D56.1 Beta thalassaemia	0.000	0.998	0.001
D56.0 Alpha thalassaemia	0.000	0.998	0.001
D57.8 Other sickle-cell disorders	0.000	0.998	0.001
D57.3 Sickle-cell trait	0.000	0.998	0.001
D57.2 Double heterozygous sickling disorders	0.000	0.998	0.001
D57.1 Sickle-cell anaemia without crisis	0.000	0.998	0.001
D57.0 Sickle-cell anaemia with crisis	0.000	0.998	0.001
D63.0 Anaemia in neoplastic disease	0.002	0.998	0.000
Q39.9 Congenital malformation of oesophagus, 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
S06.81 Other intracranial injuries (with open intracranial wound)	0.001	0.998	0.000
D58.9 Hereditary haemolytic anaemia, unspecified	0.000	0.998	0.001
D58.8 Other specified hereditary haemolytic anaemias	0.000	0.998	0.001
D58.2 Other haemoglobinopathies	0.000	0.998	0.001
D58.1 Hereditary elliptocytosis	0.000	0.998	0.001
K57.8 Diverticular disease of intestine, part unspecified, with perforation and abscess	0.000	0.998	0.002
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
Q61.9 Cystic kidney disease, unspecified	0.001	0.998	0.000
Q61.8 Other cystic kidney diseases	0.001	0.998	0.000
Q61.5 Medullary cystic kidney	0.001	0.998	0.000
Q61.4 Renal dysplasia	0.001	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.001	0.998	0.000
C67.9 Bladder, unspecified	0.000	0.998	0.002
Q61.2 Polycystic kidney, adult type	0.002	0.998	0.000
D03 Melanoma in situ	0.000	0.998	0.002
D58.0 Hereditary spherocytosis	0.000	0.998	0.001
S02.40 Fracture of malar and maxillary bones (closed)	0.002	0.998	0.000
Z36.3 Antenatal screening for malformations using ultrasound and other physical methods	0.002	0.998	0.000
D03.3 Melanoma in situ of other and unspecified parts of face	0.000	0.998	0.002
Q43.9 Congenital malformation of intestine, unspecified	0.001	0.998	0.000
T85.7 Infection and inflammatory reaction due to other internal prosthetic devices, implants and grafts	0.000	0.998	0.002
N19 Unspecified renal failure	0.000	0.998	0.002
S06.20 Diffuse brain injury (without open intracranial wound)	0.001	0.998	0.000
D03.6 Melanoma in situ of upper limb, including shoulder	0.000	0.998	0.002
Q60.0 Renal agenesis, unilateral	0.001	0.998	0.000
R60 Oedema, not elsewhere classified	0.000	0.998	0.002
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.000	0.998	0.002
I34.1 Mitral (valve) prolapse	0.000	0.998	0.002
Q38.8 Other congenital malformations of pharynx	0.001	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.001	0.998	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.001	0.998	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.001	0.998	0.000
Q38.3 Other congenital malformations of tongue	0.001	0.998	0.000
Q38.2 Macroglossia	0.001	0.998	0.000
Q38.1 Ankyloglossia	0.001	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.001	0.998	0.000
Q60.6 Potter's syndrome	0.001	0.998	0.000
Q60.5 Renal hypoplasia, unspecified	0.001	0.998	0.000
Q60.4 Renal hypoplasia, bilateral	0.001	0.998	0.000
Q60.3 Renal hypoplasia, unilateral	0.001	0.998	0.000
Q60.2 Renal agenesis, unspecified	0.001	0.998	0.000
Q60.1 Renal agenesis, bilateral	0.001	0.998	0.000
D60 Acquired pure red cell aplasia [erythroblastopenia]	0.000	0.998	0.001
S32.00 Fracture of lumbar vertebra (closed)	0.002	0.998	0.000
D59.8 Other acquired haemolytic anaemias	0.000	0.998	0.001
D59.6 Haemoglobinuria due to haemolysis from other external causes	0.000	0.998	0.001
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]	0.000	0.998	0.001
D59.4 Other nonautoimmune haemolytic anaemias	0.000	0.998	0.001
D59.3 Haemolytic-uraemic syndrome	0.000	0.998	0.001
D59.2 Drug-induced nonautoimmune haemolytic anaemia	0.000	0.998	0.001
D59.0 Drug-induced autoimmune haemolytic anaemia	0.000	0.998	0.001
F45.8 Other somatoform disorders	0.000	0.998	0.002
Q62.8 Other congenital malformations of ureter	0.001	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.001	0.998	0.000
Q62.6 Malposition of ureter	0.001	0.998	0.000
Q62.5 Duplication of ureter	0.001	0.998	0.000
Q62.4 Agenesis of ureter	0.001	0.998	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.001	0.998	0.000
Q62.2 Congenital megaloureter	0.001	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.001	0.998	0.000
Q62.0 Congenital hydronephrosis	0.001	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.001	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.001	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.001	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.001	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.001	0.998	0.000
Q64.4 Malformation of urachus	0.001	0.998	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.001	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.001	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.001	0.998	0.000
Q64.0 Epispadias	0.001	0.998	0.000
K57 Diverticular disease of intestine	0.000	0.998	0.002
M70.65 Trochanteric bursitis-Pelvic/Thigh	0.001	0.998	0.000
T84.8 Other complications of internal orthopaedic prosthetic devices, implants and grafts	0.000	0.998	0.002
D04 Carcinoma in situ of skin	0.000	0.998	0.001
D02 Carcinoma in situ of middle ear and respiratory system	0.000	0.998	0.001
D01 Carcinoma in situ of other and unspecified digestive organs	0.000	0.998	0.001
D00 Carcinoma in situ of oral cavity, oesophagus and stomach	0.000	0.998	0.001
D70-D77 Other diseases of blood and blood-forming organs	0.000	0.998	0.001
T85.4 Mechanical complication of breast prosthesis and implant	0.000	0.998	0.001
S06.00 Concussion (without open intracranial wound)	0.001	0.998	0.000
D04.7 Skin of lower limb, including hip	0.000	0.998	0.001
D04.3 Skin of other and unspecified parts of face	0.000	0.998	0.001
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.001	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.001	0.998	0.000
Q40.1 Congenital hiatus hernia	0.001	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	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
Q43.8 Other specified congenital malformations of intestine	0.001	0.998	0.000
Q43.7 Persistent cloaca	0.001	0.998	0.000
Q43.6 Congenital fistula of rectum and anus	0.001	0.998	0.000
Q43.5 Ectopic anus	0.001	0.998	0.000
Q43.4 Duplication of intestine	0.001	0.998	0.000
Q43.3 Congenital malformations of intestinal fixation	0.001	0.998	0.000
Q43.2 Other congenital functional disorders of colon	0.001	0.998	0.000
Q43.1 Hirschsprung's disease	0.001	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.001	0.998	0.000
Q45.8 Other specified congenital malformations of digestive system	0.001	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.001	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.001	0.998	0.000
Q45.1 Annular pancreas	0.001	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.001	0.998	0.000
R60.9 Oedema, unspecified	0.000	0.998	0.001
M86.97 Osteomyelitis, unspecified (Ankle and foot)	0.000	0.999	0.001
S06.80 Other intracranial injuries (without open intracranial wound)	0.001	0.999	0.000
D59.1 Other autoimmune haemolytic anaemias	0.000	0.999	0.001
D03.9 Melanoma in situ, unspecified	0.000	0.999	0.001
D03.8 Melanoma in situ of other sites	0.000	0.999	0.001
D03.1 Melanoma in situ of eyelid, including canthus	0.000	0.999	0.001
D03.0 Melanoma in situ of lip	0.000	0.999	0.001
D04.6 Skin of upper limb, including shoulder	0.000	0.999	0.001
S82.8 Fractures of other parts of lower leg	0.001	0.999	0.000
M50.2 Other cervical disk displacement	0.000	0.999	0.001
D66 Hereditary factor VIII deficiency	0.000	0.999	0.001
G11 Hereditary ataxia	0.001	0.999	0.000
B95.6 Staphylococcus aureus as the cause of diseases classified to other chapters	0.000	0.999	0.001
D03.5 Melanoma in situ of trunk	0.000	0.999	0.001
D03.4 Melanoma in situ of scalp and neck	0.000	0.999	0.001
O32.1 Maternal care for breech presentation	0.001	0.999	0.000
T85.2 Mechanical complication of intraocular lens	0.000	0.999	0.001
Z30.5 Surveillance of (intra-uterine) contraceptive device	0.000	0.999	0.001
Z51.3 Blood transfusion without reported diagnosis	0.001	0.999	0.000
D59.9 Acquired haemolytic anaemia, unspecified	0.000	0.999	0.001
Q43.0 Meckel's diverticulum	0.001	0.999	0.000
Q61.0 Congenital single renal cyst	0.001	0.999	0.000
K81 Cholecystitis	0.001	0.999	0.000
D03.7 Melanoma in situ of lower limb, including hip	0.000	0.999	0.001
D72.8 Other specified disorders of white blood cells	0.001	0.999	0.000
G51.3 Clonic hemifacial spasm	0.001	0.999	0.000
D67 Hereditary factor IX deficiency	0.000	0.999	0.001
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.000	0.999	0.001
N17-N19 Renal failure	0.000	0.999	0.001
D60.9 Acquired pure red cell aplasia, unspecified	0.000	0.999	0.001
D60.8 Other acquired pure red cell aplasias	0.000	0.999	0.001
D60.1 Transient acquired pure red cell aplasia	0.000	0.999	0.001
D60.0 Chronic acquired pure red cell aplasia	0.000	0.999	0.001
K57.4 Diverticular disease of both small and large intestine with perforation and abscess	0.000	0.999	0.001
K85.9 Acute pancreatitis, unspecified	0.001	0.999	0.000
K85.1 Biliary acute pancreatitis	0.001	0.999	0.000
D63 Anaemia in chronic diseases classified elsewhere	0.001	0.999	0.001
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.000	0.999	0.001
G51 Facial nerve disorders	0.001	0.999	0.000
M76.67 Achilles tendinitis (Ankle and foot)	0.001	0.999	0.000
D00.2 Stomach	0.000	0.999	0.001
D00.1 Oesophagus	0.000	0.999	0.001
D00.0 Lip, oral cavity and pharynx	0.000	0.999	0.001
D01.9 Digestive organ, unspecified	0.000	0.999	0.001
D01.7 Other specified digestive organs	0.000	0.999	0.001
D01.5 Liver, gallbladder and bile ducts	0.000	0.999	0.001
D01.4 Other and unspecified parts of intestine	0.000	0.999	0.001
D01.3 Anus and anal canal	0.000	0.999	0.001
D01.2 Rectum	0.000	0.999	0.001
D01.1 Rectosigmoid junction	0.000	0.999	0.001
D01.0 Colon	0.000	0.999	0.001
D02.4 Respiratory system, unspecified	0.000	0.999	0.001
D02.3 Other parts of respiratory system	0.000	0.999	0.001
D02.2 Bronchus and lung	0.000	0.999	0.001
D02.1 Trachea	0.000	0.999	0.001
D02.0 Larynx	0.000	0.999	0.001
D04.9 Skin, unspecified	0.000	0.999	0.001
D04.8 Skin of other sites	0.000	0.999	0.001
D04.1 Skin of eyelid, including canthus	0.000	0.999	0.001
D04.0 Skin of lip	0.000	0.999	0.001
K29.1 Other acute gastritis	0.000	0.999	0.001
K57.2 Diverticular disease of large intestine with perforation and abscess	0.000	0.999	0.001
N76.2 Acute vulvitis	0.001	0.999	0.000
D74 Methaemoglobinaemia	0.000	0.999	0.001
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere	0.000	0.999	0.001
D71 Functional disorders of polymorphonuclear neutrophils	0.000	0.999	0.001
H81.1 Benign paroxysmal vertigo	0.001	0.999	0.000
K57.5 Diverticular disease of both small and large intestine without perforation or abscess	0.000	0.999	0.001
K81.8 Other cholecystitis	0.001	0.999	0.000
R60.1 Generalised oedema	0.000	0.999	0.001
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.001	0.999	0.000
S82.81 Fractures of other parts of lower leg (open)	0.001	0.999	0.000
Q15.0 Congenital glaucoma	0.001	0.999	0.000
Z51.2 Other chemotherapy	0.000	0.999	0.001
S82.86 Maisonneuve's fracture	0.001	0.999	0.000
D75.1 Secondary polycythaemia	0.000	0.999	0.001
N76.4 Abscess of vulva	0.001	0.999	0.000
Q87.4 Marfan's syndrome	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