TreeWAS – Variant ID: rs73157010

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
G47.9 Sleep disorder, unspecified	0.000	0.964	0.036
G47.3 Sleep apnoea	0.000	0.964	0.036
G47 Sleep disorders	0.000	0.966	0.034
G47.1 Disorders of excessive somnolence [hypersomnias]	0.000	0.973	0.027
G47.4 Narcolepsy and cataplexy	0.000	0.975	0.024
G47.2 Disorders of the sleep-wake schedule	0.000	0.975	0.024
G40.3 Generalised idiopathic epilepsy and epileptic syndromes	0.000	0.977	0.023
G40 Epilepsy	0.000	0.978	0.022
G47.8 Other sleep disorders	0.000	0.979	0.021
G40.9 Epilepsy, unspecified	0.000	0.980	0.020
G40-G47 Episodic and paroxysmal disorders	0.000	0.980	0.020
G47.0 Disorders of initiating and maintaining sleep [insomnias]	0.000	0.981	0.019
G40.7 Petit mal, unspecified, without grand mal seizures	0.000	0.984	0.016
G40.5 Special epileptic syndromes	0.000	0.984	0.016
G40.4 Other generalised epilepsy and epileptic syndromes	0.000	0.984	0.016
G40.1 Localisation-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures	0.000	0.984	0.016
G40.0 Localisation-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localised onset	0.000	0.984	0.016
G40.8 Other epilepsy	0.000	0.984	0.015
G46 Vascular syndromes of brain in cerebrovascular diseases	0.000	0.986	0.014
G40.2 Localisation-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures	0.000	0.986	0.014
G41 Status epilepticus	0.000	0.986	0.014
G40.6 Grand mal seizures, unspecified (with or without petit mal)	0.000	0.986	0.014
G44 Other headache syndromes	0.000	0.989	0.011
G46.8 Other vascular syndromes of brain in cerebrovascular diseases	0.000	0.989	0.010
G46.7 Other lacunar syndromes	0.000	0.989	0.010
G46.6 Pure sensory lacunar syndrome	0.000	0.989	0.010
G46.5 Pure motor lacunar syndrome	0.000	0.989	0.010
G46.4 Cerebellar stroke syndrome	0.000	0.989	0.010
G46.3 Brain stem stroke syndrome	0.000	0.989	0.010
G46.2 Posterior cerebral artery syndrome	0.000	0.989	0.010
G46.1 Anterior cerebral artery syndrome	0.000	0.989	0.010
G46.0 Middle cerebral artery syndrome	0.000	0.989	0.010
G41.8 Other status epilepticus	0.000	0.990	0.010
G41.2 Complex partial status epilepticus	0.000	0.990	0.010
G41.1 Petit mal status epilepticus	0.000	0.990	0.010
G41.0 Grand mal status epilepticus	0.000	0.990	0.010
G41.9 Status epilepticus, unspecified	0.000	0.990	0.010
G43 Migraine	0.000	0.991	0.009
G44.2 Tension-type headache	0.000	0.991	0.009
G44.3 Chronic posttraumatic headache	0.000	0.992	0.008
G44.1 Vascular headache, not elsewhere classified	0.000	0.992	0.008
G44.8 Other specified headache syndromes	0.000	0.992	0.008
G43.1 Migraine with aura [classical migraine]	0.000	0.993	0.007
R47.8 Other and unspecified speech disturbances	0.007	0.993	0.000
G44.4 Drug-induced headache, not elsewhere classified	0.000	0.993	0.007
K35.9 Acute appendicitis, unspecified	0.000	0.993	0.007
R47 Speech disturbances, not elsewhere classified	0.007	0.993	0.000
G43.3 Complicated migraine	0.000	0.993	0.007
G43.2 Status migrainosus	0.000	0.993	0.007
G43.0 Migraine without aura [common migraine]	0.000	0.993	0.007
R47.0 Dysphasia and aphasia	0.007	0.993	0.000
G43.8 Other migraine	0.000	0.993	0.007
G45 Transient cerebral ischaemic attacks and related syndromes	0.000	0.994	0.006
G44.0 Cluster headache syndrome	0.000	0.994	0.006
R47.1 Dysarthria and anarthria	0.006	0.994	0.000
D75.2 Essential thrombocytosis	0.005	0.995	0.000
D75 Other diseases of blood and blood-forming organs	0.005	0.995	0.000
M19.94 Arthrosis, unspecified (Hand)	0.000	0.995	0.005
R49.0 Dysphonia	0.005	0.995	0.000
R49 Voice disturbances	0.005	0.995	0.000
G45.8 Other transient cerebral ischaemic attacks and related syndromes	0.000	0.995	0.005
D75.1 Secondary polycythaemia	0.005	0.995	0.000
R47-R49 Symptoms and signs involving speech and voice	0.005	0.995	0.000
H53.9 Visual disturbance, unspecified	0.005	0.995	0.000
G45.2 Multiple and bilateral precerebral artery syndromes	0.000	0.995	0.005
G45.1 Carotid artery syndrome (hemispheric)	0.000	0.995	0.005
G45.0 Vertebro-basilar artery syndrome	0.000	0.995	0.005
M89.97 Disorder of bone, unspecified (Ankle and foot)	0.005	0.995	0.000
D75.8 Other specified diseases of blood and blood-forming organs	0.004	0.995	0.000
K35 Acute appendicitis	0.000	0.995	0.005
D70-D77 Other diseases of blood and blood-forming organs	0.005	0.995	0.000
D70 Agranulocytosis	0.005	0.995	0.000
M89.9 Disorder of bone, unspecified	0.004	0.995	0.000
N95.8 Other specified menopausal and perimenopausal disorders	0.004	0.995	0.000
O70.0 First degree perineal laceration during delivery	0.000	0.996	0.004
K60.3 Anal fistula	0.004	0.996	0.000
R49.8 Other and unspecified voice disturbances	0.004	0.996	0.000
S01.5 Open wound of lip and oral cavity	0.004	0.996	0.000
G45.3 Amaurosis fugax	0.000	0.996	0.004
D75.0 Familial erythrocytosis	0.004	0.996	0.000
K35.1 Acute appendicitis with peritoneal abscess	0.000	0.996	0.004
K22.1 Ulcer of oesophagus	0.000	0.996	0.004
K35.8 Acute appendicitis, other and unspecified	0.000	0.996	0.004
M89.98 Disorder of bone, unspecified (Other)	0.004	0.996	0.000
R49.2 Hypernasality and hyponasality	0.004	0.996	0.000
R49.1 Aphonia	0.004	0.996	0.000
M89.94 Disorder of bone, unspecified (Hand)	0.004	0.996	0.000
R48 Dyslexia and other symbolic dysfunctions, not elsewhere classified	0.004	0.996	0.000
Z02.8 Other examinations for administrative purposes	0.004	0.996	0.000
K35.3 Acute appendicitis with localized peritonitis	0.000	0.996	0.004
D72 Other disorders of white blood cells	0.004	0.996	0.000
M89.96 Disorder of bone, unspecified (Lower leg)	0.004	0.996	0.000
Q61.2 Polycystic kidney, adult type	0.004	0.996	0.000
Q61 Cystic kidney disease	0.004	0.996	0.000
M89.95 Disorder of bone, unspecified (Pelvic region and thigh)	0.004	0.996	0.000
D75.9 Disease of blood and blood-forming organs, unspecified	0.003	0.996	0.000
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.004	0.996	0.000
D86 Sarcoidosis	0.004	0.996	0.000
D80-D89 Certain disorders involving the immune mechanism	0.004	0.996	0.000
Q60-Q64 Congenital malformations of the urinary system	0.004	0.996	0.000
D74 Methaemoglobinaemia	0.003	0.996	0.000
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere	0.003	0.996	0.000
D71 Functional disorders of polymorphonuclear neutrophils	0.003	0.996	0.000
D86.9 Sarcoidosis, unspecified	0.003	0.996	0.000
Q61.3 Polycystic kidney, unspecified	0.003	0.996	0.000
M89.99 Disorder of bone, unspecified (Site unspecified)	0.003	0.996	0.000
M89.93 Disorder of bone, unspecified (Forearm)	0.003	0.996	0.000
M89.92 Disorder of bone, unspecified (Upper arm)	0.003	0.996	0.000
M89.91 Disorder of bone, unspecified (Shoulder region)	0.003	0.996	0.000
M89.90 Disorder of bone, unspecified (Multiple sites)	0.003	0.996	0.000
Q63 Other congenital malformations of kidney	0.003	0.997	0.000
M89 Other disorders of bone	0.003	0.997	0.000
Q63.0 Accessory kidney	0.003	0.997	0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.003	0.997	0.000
M35.0 Sicca syndrome [Sjogren]	0.003	0.997	0.000
K35.0 Acute appendicitis with generalised peritonitis	0.000	0.997	0.003
D72.8 Other specified disorders of white blood cells	0.003	0.997	0.000
M89.8 Other specified disorders of bone	0.003	0.997	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.003	0.997	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.003	0.997	0.000
Q64 Other congenital malformations of urinary system	0.003	0.997	0.000
R48.8 Other and unspecified symbolic dysfunctions	0.003	0.997	0.000
R48.2 Apraxia	0.003	0.997	0.000
R48.1 Agnosia	0.003	0.997	0.000
R48.0 Dyslexia and alexia	0.003	0.997	0.000
D86.8 Sarcoidosis of other and combined sites	0.003	0.997	0.000
D73 Diseases of spleen	0.003	0.997	0.000
K35.2 Acute appendicitis with generalized peritonitis	0.000	0.997	0.003
D80 Immunodeficiency with predominantly antibody defects	0.003	0.997	0.000
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.003	0.997	0.000
D72.9 Disorder of white blood cells, unspecified	0.003	0.997	0.000
D72.1 Eosinophilia	0.003	0.997	0.000
D72.0 Genetic anomalies of leukocytes	0.003	0.997	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.003	0.997	0.000
D76.3 Other histiocytosis syndromes	0.003	0.997	0.000
G45.4 Transient global amnesia	0.000	0.997	0.002
M75.4 Impingement syndrome of shoulder	0.003	0.997	0.000
Q61.9 Cystic kidney disease, unspecified	0.003	0.997	0.000
Q61.8 Other cystic kidney diseases	0.003	0.997	0.000
Q61.5 Medullary cystic kidney	0.003	0.997	0.000
Q61.4 Renal dysplasia	0.003	0.997	0.000
Q61.1 Polycystic kidney, infantile type	0.003	0.997	0.000
D86.1 Sarcoidosis of lymph nodes	0.003	0.997	0.000
D76.2 Haemophagocytic syndrome, infection-associated	0.003	0.997	0.000
D76.1 Haemophagocytic lymphohistiocytosis	0.003	0.997	0.000
D76.0 Langerhans' cell histiocytosis, not elsewhere classified	0.003	0.997	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.003	0.997	0.000
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
D84 Other immunodeficiencies	0.003	0.997	0.000
D83 Common variable immunodeficiency	0.003	0.997	0.000
D82 Immunodeficiency associated with other major defects	0.003	0.997	0.000
D81 Combined immunodeficiencies	0.003	0.997	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.003	0.997	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.003	0.997	0.000
D74.9 Methaemoglobinaemia, unspecified	0.003	0.997	0.000
D74.8 Other methaemoglobinaemias	0.003	0.997	0.000
D74.0 Congenital methaemoglobinaemia	0.003	0.997	0.000
D86.0 Sarcoidosis of lung	0.003	0.997	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.003	0.997	0.000
Q63.8 Other specified congenital malformations of kidney	0.003	0.997	0.000
Q63.3 Hyperplastic and giant kidney	0.003	0.997	0.000
Q63.2 Ectopic kidney	0.003	0.997	0.000
M89.6 Osteopathy after poliomyelitis	0.003	0.997	0.000
M89.5 Osteolysis	0.003	0.997	0.000
M89.4 Other hypertrophic osteo-arthropathy	0.003	0.997	0.000
M89.3 Hypertrophy of bone	0.003	0.997	0.000
M89.2 Other disorders of bone development and growth	0.003	0.997	0.000
M89.1 Epiphyseal arrest	0.003	0.997	0.000
M89.0 Algoneurodystrophy	0.003	0.997	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.003	0.997	0.000
M77.91 Enthesopathy, unspecified (Shoulder region)	0.003	0.997	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.003	0.997	0.000
D89.3 Immune reconstitution syndrome	0.003	0.997	0.000
D89.1 Cryoglobulinaemia	0.003	0.997	0.000
D89.0 Polyclonal hypergammaglobulinaemia	0.003	0.997	0.000
M89.86 Other specified disorders of bone (Lower leg)	0.003	0.997	0.000
M89.85 Other specified disorders of bone (Pelvic region and thigh)	0.003	0.997	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.003	0.997	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.003	0.997	0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.003	0.997	0.000
Q44.6 Cystic disease of liver	0.003	0.997	0.000
M35.3 Polymyalgia rheumatica	0.003	0.997	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.997	0.000
D69 Purpura and other haemorrhagic conditions	0.003	0.997	0.000
Q38.7 Pharyngeal pouch	0.002	0.997	0.000
M35 Other systemic involvement of connective tissue	0.003	0.997	0.000
D80.1 Nonfamilial hypogammaglobulinaemia	0.002	0.997	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
D69.0 Allergic purpura	0.003	0.997	0.000
D69.9 Haemorrhagic condition, unspecified	0.002	0.997	0.000
M89.89 Other specified disorders of bone (Site unspecified)	0.002	0.997	0.000
M89.88 Other specified disorders of bone (Other)	0.002	0.997	0.000
M89.87 Other specified disorders of bone (Ankle and foot)	0.002	0.997	0.000
M89.84 Other specified disorders of bone (Hand)	0.002	0.997	0.000
M89.83 Other specified disorders of bone (Forearm)	0.002	0.997	0.000
M89.82 Other specified disorders of bone (Upper arm)	0.002	0.997	0.000
M89.81 Other specified disorders of bone (Shoulder region)	0.002	0.997	0.000
M89.80 Other specified disorders of bone (Multiple sites)	0.002	0.997	0.000
D73.5 Infarction of spleen	0.002	0.997	0.000
G45.9 Transient cerebral ischaemic attack, unspecified	0.000	0.997	0.002
Q43 Other congenital malformations of intestine	0.002	0.997	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.997	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.002	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.002	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.002	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.002	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.002	0.998	0.000
Q64.4 Malformation of urachus	0.002	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.002	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.002	0.998	0.000
Q64.0 Epispadias	0.002	0.998	0.000
D73.9 Disease of spleen, unspecified	0.002	0.998	0.000
D73.8 Other diseases of spleen	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
T18.1 Foreign body in oesophagus	0.002	0.998	0.000
M77.57 Other enthesopathy of foot-Ankle/Foot	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
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.002	0.998	0.000
D80.0 Hereditary hypogammaglobulinaemia	0.002	0.998	0.000
Q61.0 Congenital single renal cyst	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
M77.9 Enthesopathy, unspecified	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
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
Q76 Congenital malformations of spine and bony thorax	0.002	0.998	0.000
D69.5 Secondary thrombocytopenia	0.002	0.998	0.000
Q24 Other congenital malformations of heart	0.002	0.998	0.000
Q23 Congenital malformations of aortic and mitral valves	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
D84.9 Immunodeficiency, unspecified	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
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
Q62.8 Other congenital malformations of ureter	0.002	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.002	0.998	0.000
Q62.6 Malposition of ureter	0.002	0.998	0.000
Q62.5 Duplication of ureter	0.002	0.998	0.000
Q62.4 Agenesis of ureter	0.002	0.998	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.002	0.998	0.000
Q62.2 Congenital megaloureter	0.002	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.002	0.998	0.000
Q62.0 Congenital hydronephrosis	0.002	0.998	0.000
M79.62 Pain in limb (Upper arm)	0.002	0.998	0.000
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.002	0.998	0.000
D55-D59 Haemolytic anaemias	0.002	0.998	0.000
M89.09 Algoneurodystrophy (Site unspecified)	0.002	0.998	0.000
M89.08 Algoneurodystrophy (Other)	0.002	0.998	0.000
M89.07 Algoneurodystrophy (Ankle and foot)	0.002	0.998	0.000
M89.06 Algoneurodystrophy (Lower leg)	0.002	0.998	0.000
M89.05 Algoneurodystrophy (Pelvic region and thigh)	0.002	0.998	0.000
M89.04 Algoneurodystrophy (Hand)	0.002	0.998	0.000
M89.03 Algoneurodystrophy (Forearm)	0.002	0.998	0.000
M89.02 Algoneurodystrophy (Upper arm)	0.002	0.998	0.000
M89.01 Algoneurodystrophy (Shoulder region)	0.002	0.998	0.000
M89.00 Algoneurodystrophy (Multiple sites)	0.002	0.998	0.000
M89.19 Epiphyseal arrest (Site unspecified)	0.002	0.998	0.000
M89.18 Epiphyseal arrest (Other)	0.002	0.998	0.000
M89.17 Epiphyseal arrest (Ankle and foot)	0.002	0.998	0.000
M89.16 Epiphyseal arrest (Lower leg)	0.002	0.998	0.000
M89.15 Epiphyseal arrest (Pelvic region and thigh)	0.002	0.998	0.000
M89.14 Epiphyseal arrest (Hand)	0.002	0.998	0.000
M89.13 Epiphyseal arrest (Forearm)	0.002	0.998	0.000
M89.12 Epiphyseal arrest (Upper arm)	0.002	0.998	0.000
M89.11 Epiphyseal arrest (Shoulder region)	0.002	0.998	0.000
M89.10 Epiphyseal arrest (Multiple sites)	0.002	0.998	0.000
M89.29 Other disorders of bone development and growth (Site unspecified)	0.002	0.998	0.000
M89.28 Other disorders of bone development and growth (Other)	0.002	0.998	0.000
M89.27 Other disorders of bone development and growth (Ankle and foot)	0.002	0.998	0.000
M89.26 Other disorders of bone development and growth (Lower leg)	0.002	0.998	0.000
M89.25 Other disorders of bone development and growth (Pelvic region and thigh)	0.002	0.998	0.000
M89.24 Other disorders of bone development and growth (Hand)	0.002	0.998	0.000
M89.23 Other disorders of bone development and growth (Forearm)	0.002	0.998	0.000
M89.22 Other disorders of bone development and growth (Upper arm)	0.002	0.998	0.000
M89.21 Other disorders of bone development and growth (Shoulder region)	0.002	0.998	0.000
M89.20 Other disorders of bone development and growth (Multiple sites)	0.002	0.998	0.000
M89.39 Hypertrophy of bone (Site unspecified)	0.002	0.998	0.000
M89.38 Hypertrophy of bone (Other)	0.002	0.998	0.000
M89.37 Hypertrophy of bone (Ankle and foot)	0.002	0.998	0.000
M89.36 Hypertrophy of bone (Lower leg)	0.002	0.998	0.000
M89.35 Hypertrophy of bone (Pelvic region and thigh)	0.002	0.998	0.000
M89.34 Hypertrophy of bone (Hand)	0.002	0.998	0.000
M89.33 Hypertrophy of bone (Forearm)	0.002	0.998	0.000
M89.32 Hypertrophy of bone (Upper arm)	0.002	0.998	0.000
M89.31 Hypertrophy of bone (Shoulder region)	0.002	0.998	0.000
M89.30 Hypertrophy of bone (Multiple sites)	0.002	0.998	0.000
M89.49 Other hypertrophic osteoarthropathy (Site unspecified)	0.002	0.998	0.000
M89.48 Other hypertrophic osteoarthropathy (Other)	0.002	0.998	0.000
M89.47 Other hypertrophic osteoarthropathy (Ankle and foot)	0.002	0.998	0.000
M89.46 Other hypertrophic osteoarthropathy (Lower leg)	0.002	0.998	0.000
M89.45 Other hypertrophic osteoarthropathy (Pelvic region and thigh)	0.002	0.998	0.000
M89.44 Other hypertrophic osteoarthropathy (Hand)	0.002	0.998	0.000
M89.43 Other hypertrophic osteoarthropathy (Forearm)	0.002	0.998	0.000
M89.42 Other hypertrophic osteoarthropathy (Upper arm)	0.002	0.998	0.000
M89.41 Other hypertrophic osteoarthropathy (Shoulder region)	0.002	0.998	0.000
M89.40 Other hypertrophic osteoarthropathy (Multiple sites)	0.002	0.998	0.000
M89.59 Osteolysis (Site unspecified)	0.002	0.998	0.000
M89.58 Osteolysis (Other)	0.002	0.998	0.000
M89.57 Osteolysis (Ankle and foot)	0.002	0.998	0.000
M89.56 Osteolysis (Lower leg)	0.002	0.998	0.000
M89.55 Osteolysis (Pelvic region and thigh)	0.002	0.998	0.000
M89.54 Osteolysis (Hand)	0.002	0.998	0.000
M89.53 Osteolysis (Forearm)	0.002	0.998	0.000
M89.52 Osteolysis (Upper arm)	0.002	0.998	0.000
M89.51 Osteolysis (Shoulder region)	0.002	0.998	0.000
M89.50 Osteolysis (Multiple sites)	0.002	0.998	0.000
M89.69 Osteopathy after poliomyelitis (Site unspecified)	0.002	0.998	0.000
M89.68 Osteopathy after poliomyelitis (Other)	0.002	0.998	0.000
M89.67 Osteopathy after poliomyelitis (Ankle and foot)	0.002	0.998	0.000
M89.66 Osteopathy after poliomyelitis (Lower leg)	0.002	0.998	0.000
M89.65 Osteopathy after poliomyelitis (Pelvic region and thigh)	0.002	0.998	0.000
M89.64 Osteopathy after poliomyelitis (Hand)	0.002	0.998	0.000
M89.63 Osteopathy after poliomyelitis (Forearm)	0.002	0.998	0.000
M89.62 Osteopathy after poliomyelitis (Upper arm)	0.002	0.998	0.000
M89.61 Osteopathy after poliomyelitis (Shoulder region)	0.002	0.998	0.000
M89.60 Osteopathy after poliomyelitis (Multiple sites)	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
M77.5 Other enthesopathy of foot	0.002	0.998	0.000
Q38.8 Other congenital malformations of pharynx	0.002	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.998	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.002	0.998	0.000
Q38.3 Other congenital malformations of tongue	0.002	0.998	0.000
Q38.2 Macroglossia	0.002	0.998	0.000
Q38.1 Ankyloglossia	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
D67 Hereditary factor IX deficiency	0.002	0.998	0.000
D66 Hereditary factor VIII deficiency	0.002	0.998	0.000
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.002	0.998	0.000
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
Q43.8 Other specified congenital malformations of intestine	0.002	0.998	0.000
D68.2 Hereditary deficiency of other clotting factors	0.002	0.998	0.000
Q60.6 Potter's syndrome	0.002	0.998	0.000
Q60.5 Renal hypoplasia, unspecified	0.002	0.998	0.000
Q60.4 Renal hypoplasia, bilateral	0.002	0.998	0.000
Q60.3 Renal hypoplasia, unilateral	0.002	0.998	0.000
Q60.2 Renal agenesis, unspecified	0.002	0.998	0.000
Q60.1 Renal agenesis, bilateral	0.002	0.998	0.000
R73.0 Abnormal glucose tolerance test	0.000	0.998	0.002
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
D69.8 Other specified haemorrhagic conditions	0.002	0.998	0.000
D69.4 Other primary thrombocytopenia	0.002	0.998	0.000
D69.2 Other nonthrombocytopenic purpura	0.002	0.998	0.000
D69.1 Qualitative platelet defects	0.002	0.998	0.000
Q23.1 Congenital insufficiency of aortic valve	0.002	0.998	0.000
M35.9 Systemic involvement of connective tissue, unspecified	0.002	0.998	0.000
M35.8 Other specified systemic involvement of connective tissue	0.002	0.998	0.000
M35.6 Relapsing panniculitis [Weber-Christian]	0.002	0.998	0.000
M35.5 Multifocal fibrosclerosis	0.002	0.998	0.000
M35.4 Diffuse (eosinophilic) fasciitis	0.002	0.998	0.000
M35.2 Behcet's disease	0.002	0.998	0.000
M35.1 Other overlap syndromes	0.002	0.998	0.000
D62 Acute posthaemorrhagic anaemia	0.002	0.998	0.000
M77 Other enthesopathies	0.002	0.998	0.000
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q25 Congenital malformations of great arteries	0.002	0.998	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
D60-D64 Aplastic and other anaemias	0.002	0.998	0.000
M86-M90 Other osteopathies	0.002	0.998	0.000
M35.7 Hypermobility syndrome	0.002	0.998	0.000
D63.0 Anaemia in neoplastic disease	0.002	0.998	0.000
Q24.8 Other specified congenital malformations of heart	0.002	0.998	0.000
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
M06.99 Rheumatoid arthritis, unspecified (Site unspecified)	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.002	0.998	0.000
Q43.7 Persistent cloaca	0.002	0.998	0.000
Q43.6 Congenital fistula of rectum and anus	0.002	0.998	0.000
Q43.5 Ectopic anus	0.002	0.998	0.000
Q43.4 Duplication of intestine	0.002	0.998	0.000
Q43.3 Congenital malformations of intestinal fixation	0.002	0.998	0.000
Q43.2 Other congenital functional disorders of colon	0.002	0.998	0.000
Q43.1 Hirschsprung's disease	0.002	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.002	0.998	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.998	0.000
Q73 Reduction defects of unspecified limb	0.002	0.998	0.000
Q72 Reduction defects of lower limb	0.002	0.998	0.000
Q71 Reduction defects of upper limb	0.002	0.998	0.000
Q70 Syndactyly	0.002	0.998	0.000
Q69 Polydactyly	0.002	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
D68 Other coagulation defects	0.002	0.998	0.000
M75 Shoulder lesions	0.002	0.998	0.000
Q05 Spina bifida	0.002	0.998	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.002	0.998	0.000
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
Q15 Other congenital malformations of eye	0.002	0.998	0.000
Q14 Congenital malformations of posterior segment of eye	0.002	0.998	0.000
Q13 Congenital malformations of anterior segment of eye	0.002	0.998	0.000
Q12 Congenital lens malformations	0.002	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
Q65 Congenital deformities of hip	0.002	0.998	0.000
M77.99 Enthesopathy, unspecified (Site unspecified)	0.002	0.998	0.000
M77.98 Enthesopathy, unspecified (Other)	0.002	0.998	0.000
M77.97 Enthesopathy, unspecified (Ankle and foot)	0.002	0.998	0.000
M77.96 Enthesopathy, unspecified (Lower leg)	0.002	0.998	0.000
M77.95 Enthesopathy, unspecified (Pelvic region and thigh)	0.002	0.998	0.000
M77.94 Enthesopathy, unspecified (Hand)	0.002	0.998	0.000
M77.93 Enthesopathy, unspecified (Forearm)	0.002	0.998	0.000
M77.92 Enthesopathy, unspecified (Upper arm)	0.002	0.998	0.000
M77.90 Enthesopathy, unspecified (Multiple sites)	0.002	0.998	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.002	0.998	0.000
Q39.8 Other congenital malformations of oesophagus	0.002	0.998	0.000
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.002	0.998	0.000
Q39.4 Oesophageal web	0.002	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.002	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.002	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.002	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.998	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.002	0.998	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.002	0.998	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.002	0.998	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.002	0.998	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.002	0.998	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.002	0.998	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.002	0.998	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.002	0.998	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.002	0.998	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.002	0.998	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.002	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.002	0.998	0.000
Q45.8 Other specified congenital malformations of digestive system	0.002	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.002	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.002	0.998	0.000
Q45.1 Annular pancreas	0.002	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.002	0.998	0.000
K60 Fissure and fistula of anal and rectal regions	0.002	0.998	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
M23.81 Other internal derangements of knee (Anterior cruciate ligament or Anterior horn of medial meniscus)	0.002	0.998	0.000
K61.0 Anal abscess	0.002	0.998	0.000
Q43.0 Meckel's diverticulum	0.002	0.998	0.000
Q60.0 Renal agenesis, unilateral	0.002	0.998	0.000
Q76.0 Spina bifida occulta	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.002	0.998	0.000
Q04 Other congenital malformations of brain	0.002	0.998	0.000
Q03 Congenital hydrocephalus	0.002	0.998	0.000
Q01 Encephalocele	0.002	0.998	0.000
Q00 Anencephaly and similar malformations	0.002	0.998	0.000
Q02 Microcephaly	0.002	0.998	0.000
K60.5 Anorectal fistula	0.002	0.998	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.002	0.998	0.000

This table lists the top 500 terms ordered by p(effect).

The full results table can be downloaded from this page.

The TreeWAS Database is the result of research conducted at the Oxford Big Data Institute at the University of Oxford.

This research has been conducted using the UK Biobank Resource (application number 10625). This work uses data provided by patients and collected by the NHS as part of their care and support.

This research has been conducted with the support of the Wellcome Trust (100956/Z/13/Z and 090532/Z/09/Z and 100308/Z/12/Z), the Danish National Research Foundation, Takeda, the Medical Research Council (MC_UU_12010/3), the Oak Foundation (OCAY-15-520), the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC), the Wellcome Trust/Royal Society (204290/Z/16/Z) and the Li Ka Shing Foundation.

Variant-specific associations