TreeWAS – Variant ID: rs1981491

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
D68.2 Hereditary deficiency of other clotting factors	0.000	0.000	1.000
D68 Other coagulation defects	0.000	0.138	0.862
D68.8 Other specified coagulation defects	0.000	0.158	0.842
D68.5 Primary Thrombophilia	0.000	0.289	0.711
D68.6 Other Thrombophilia	0.000	0.310	0.690
D68.3 Haemorrhagic disorder due to circulating anticoagulants	0.000	0.408	0.592
D68.1 Hereditary factor XI deficiency	0.000	0.425	0.575
D68.4 Acquired coagulation factor deficiency	0.000	0.439	0.561
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.000	0.573	0.427
D68.0 Von Willebrand's disease	0.000	0.594	0.406
D69 Purpura and other haemorrhagic conditions	0.000	0.661	0.339
D68.9 Coagulation defect, unspecified	0.000	0.673	0.327
D67 Hereditary factor IX deficiency	0.000	0.680	0.320
D66 Hereditary factor VIII deficiency	0.000	0.695	0.305
D69.5 Secondary thrombocytopenia	0.000	0.702	0.298
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.000	0.712	0.288
D69.6 Thrombocytopenia, unspecified	0.000	0.720	0.280
D69.0 Allergic purpura	0.000	0.723	0.277
D69.9 Haemorrhagic condition, unspecified	0.000	0.726	0.274
D69.1 Qualitative platelet defects	0.000	0.755	0.245
D69.8 Other specified haemorrhagic conditions	0.000	0.773	0.227
D69.2 Other nonthrombocytopenic purpura	0.000	0.774	0.226
D69.4 Other primary thrombocytopenia	0.000	0.804	0.195
Y84.2 Radiological procedure and radiotherapy	0.177	0.823	0.000
D69.3 Idiopathic thrombocytopenic purpura	0.000	0.921	0.079
H02.8 Other specified disorders of eyelid	0.000	0.949	0.051
I27.9 Pulmonary heart disease, unspecified	0.000	0.955	0.045
I27.0 Primary pulmonary hypertension	0.000	0.960	0.040
I27 Other pulmonary heart diseases	0.000	0.960	0.040
I27.8 Other specified pulmonary heart diseases	0.000	0.967	0.033
I27.1 Kyphoscoliotic heart disease	0.000	0.971	0.029
I26-I28 Pulmonary heart disease and diseases of pulmonary circulation	0.000	0.982	0.018
Y84 Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure	0.017	0.983	0.000
I27.2 Other secondary pulmonary hypertension	0.000	0.984	0.016
I28 Other diseases of pulmonary vessels	0.000	0.984	0.016
O68.2 Labour and delivery complicated by foetal heart rate anomaly with meconium in amniotic fluid	0.016	0.984	0.000
I28.8 Other specified diseases of pulmonary vessels	0.000	0.986	0.014
Y84.4 Aspiration of fluid	0.013	0.987	0.000
Y84.9 Medical procedure, unspecified	0.012	0.988	0.000
Y84.7 Blood-sampling	0.012	0.988	0.000
Y84.5 Insertion of gastric or duodenal sound	0.012	0.988	0.000
Y84.3 Shock therapy	0.012	0.988	0.000
R49.8 Other and unspecified voice disturbances	0.000	0.988	0.012
Y84.8 Other medical procedures	0.012	0.988	0.000
Y84.1 Kidney dialysis	0.012	0.988	0.000
I28.9 Disease of pulmonary vessels, unspecified	0.000	0.988	0.011
I28.1 Aneurysm of pulmonary artery	0.000	0.988	0.011
I28.0 Arteriovenous fistula of pulmonary vessels	0.000	0.988	0.011
M05.99 Seropositive rheumatoid arthritis, unspecified (Site unspecified)	0.000	0.991	0.009
L03.3 Cellulitis of trunk	0.009	0.991	0.000
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.000	0.991	0.009
I26 Pulmonary embolism	0.000	0.991	0.009
K62.4 Stenosis of anus and rectum	0.000	0.992	0.008
M05.9 Seropositive rheumatoid arthritis, unspecified	0.000	0.992	0.008
G81.9 Hemiplegia, unspecified	0.000	0.992	0.008
M05.97 Seropositive rheumatoid arthritis, unspecified (Ankle and foot)	0.000	0.993	0.007
I26.0 Pulmonary embolism with mention of acute cor pulmonale	0.000	0.993	0.007
M05.96 Seropositive rheumatoid arthritis, unspecified (Lower leg)	0.000	0.993	0.007
G81 Hemiplegia	0.000	0.993	0.006
D80-D89 Certain disorders involving the immune mechanism	0.000	0.993	0.007
G83.8 Other specified paralytic syndromes	0.000	0.994	0.006
B18.2 Chronic viral hepatitis C	0.006	0.994	0.000
M05.95 Seropositive rheumatoid arthritis, unspecified (Pelvic region and thigh)	0.000	0.994	0.006
M05.94 Seropositive rheumatoid arthritis, unspecified (Hand)	0.000	0.994	0.006
K12.1 Other forms of stomatitis	0.000	0.994	0.006
G83 Other paralytic syndromes	0.000	0.994	0.006
I63.8 Other cerebral infarction	0.000	0.994	0.006
M05.98 Seropositive rheumatoid arthritis, unspecified (Other)	0.000	0.994	0.006
M05.93 Seropositive rheumatoid arthritis, unspecified (Forearm)	0.000	0.994	0.006
M05.92 Seropositive rheumatoid arthritis, unspecified (Upper arm)	0.000	0.994	0.006
G82.5 Tetraplegia, unspecified	0.000	0.994	0.006
G80-G83 Cerebral palsy and other paralytic syndromes	0.000	0.994	0.006
D82 Immunodeficiency associated with other major defects	0.000	0.994	0.005
G82 Paraplegia and tetraplegia	0.000	0.994	0.006
M05.91 Seropositive rheumatoid arthritis, unspecified (Shoulder region)	0.000	0.995	0.005
M05.90 Seropositive rheumatoid arthritis, unspecified (Multiple sites)	0.000	0.995	0.005
G83.4 Cauda equina syndrome	0.000	0.995	0.005
D80 Immunodeficiency with predominantly antibody defects	0.000	0.995	0.005
G81.1 Spastic hemiplegia	0.000	0.995	0.005
I63.5 Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries	0.000	0.995	0.005
S01.0 Open wound of scalp	0.005	0.995	0.000
D81 Combined immunodeficiencies	0.000	0.995	0.005
G81.0 Flaccid hemiplegia	0.000	0.995	0.005
G83.2 Monoplegia of upper limb	0.000	0.995	0.005
I63 Cerebral infarction	0.000	0.995	0.005
D84 Other immunodeficiencies	0.000	0.995	0.005
B18 Chronic viral hepatitis	0.005	0.995	0.000
G82.4 Spastic tetraplegia	0.000	0.995	0.005
D82.1 Di George's syndrome	0.000	0.995	0.005
D83 Common variable immunodeficiency	0.000	0.995	0.005
G83.5 Locked-in syndrome	0.000	0.995	0.005
G83.3 Monoplegia, unspecified	0.000	0.995	0.005
G83.0 Diplegia of upper limbs	0.000	0.995	0.005
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.000	0.995	0.005
K91.3 Postoperative intestinal obstruction	0.000	0.995	0.005
G83.1 Monoplegia of lower limb	0.000	0.995	0.005
I63.4 Cerebral infarction due to embolism of cerebral arteries	0.000	0.995	0.004
D86 Sarcoidosis	0.000	0.996	0.004
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.000	0.996	0.004
G83.9 Paralytic syndrome, unspecified	0.000	0.996	0.004
D62 Acute posthaemorrhagic anaemia	0.000	0.996	0.004
D60-D64 Aplastic and other anaemias	0.000	0.996	0.004
Q24.8 Other specified congenital malformations of heart	0.004	0.996	0.000
D82.9 Immunodeficiency associated with major defect, unspecified	0.000	0.996	0.004
D82.8 Immunodeficiency associated with other specified major defects	0.000	0.996	0.004
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.000	0.996	0.004
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.000	0.996	0.004
D82.2 Immunodeficiency with short-limbed stature	0.000	0.996	0.004
D82.0 Wiskott-Aldrich syndrome	0.000	0.996	0.004
G82.3 Flaccid tetraplegia	0.000	0.996	0.004
G82.0 Flaccid paraplegia	0.000	0.996	0.004
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.000	0.996	0.004
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.000	0.996	0.004
I63.9 Cerebral infarction, unspecified	0.000	0.996	0.004
D84.9 Immunodeficiency, unspecified	0.000	0.996	0.004
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.000	0.996	0.004
Y84.0 Cardiac catheterisation	0.004	0.996	0.000
R49 Voice disturbances	0.000	0.996	0.004
B18.9 Chronic viral hepatitis, unspecified	0.004	0.996	0.000
D80.8 Other immunodeficiencies with predominantly antibody defects	0.000	0.996	0.004
D80.7 Transient hypogammaglobulinaemia of infancy	0.000	0.996	0.004
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.000	0.996	0.004
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.000	0.996	0.004
D80.0 Hereditary hypogammaglobulinaemia	0.000	0.996	0.004
I63.0 Cerebral infarction due to thrombosis of precerebral arteries	0.000	0.996	0.004
D81.9 Combined immunodeficiency, unspecified	0.000	0.996	0.004
D81.8 Other combined immunodeficiencies	0.000	0.996	0.004
D81.7 Major histocompatibility complex class II deficiency	0.000	0.996	0.004
D81.6 Major histocompatibility complex class I deficiency	0.000	0.996	0.004
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.000	0.996	0.004
D81.4 Nezelof's syndrome	0.000	0.996	0.004
D81.3 Adenosine deaminase [ADA] deficiency	0.000	0.996	0.004
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.000	0.996	0.004
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.000	0.996	0.004
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.000	0.996	0.004
M05 Seropositive rheumatoid arthritis	0.000	0.996	0.004
D89.1 Cryoglobulinaemia	0.000	0.996	0.004
G82.2 Paraplegia, unspecified	0.000	0.996	0.004
N50.8 Other specified disorders of male genital organs	0.004	0.996	0.000
D89.0 Polyclonal hypergammaglobulinaemia	0.000	0.996	0.004
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.000	0.996	0.004
I63.6 Cerebral infarction due to cerebral venous thrombosis, nonpyogenic	0.000	0.996	0.004
I63.1 Cerebral infarction due to embolism of precerebral arteries	0.000	0.996	0.004
B18.8 Other chronic viral hepatitis	0.004	0.996	0.000
B18.0 Chronic viral hepatitis B with delta-agent	0.004	0.996	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.000	0.996	0.004
D80.1 Nonfamilial hypogammaglobulinaemia	0.000	0.996	0.004
D83.8 Other common variable immunodeficiencies	0.000	0.996	0.003
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells	0.000	0.996	0.003
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders	0.000	0.996	0.003
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function	0.000	0.996	0.003
B18.1 Chronic viral hepatitis B without delta-agent	0.004	0.996	0.000
D86.1 Sarcoidosis of lymph nodes	0.000	0.996	0.004
D84.8 Other specified immunodeficiencies	0.000	0.996	0.003
D89.3 Immune reconstitution syndrome	0.000	0.996	0.003
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.000	0.997	0.003
D60 Acquired pure red cell aplasia [erythroblastopenia]	0.000	0.997	0.003
R49.1 Aphonia	0.000	0.997	0.003
D86.8 Sarcoidosis of other and combined sites	0.000	0.997	0.003
D83.9 Common variable immunodeficiency, unspecified	0.000	0.997	0.003
B15-B19 Viral hepatitis	0.003	0.997	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.000	0.997	0.003
G82.1 Spastic paraplegia	0.000	0.997	0.003
T45.0 Antiallergic and antiemetic drugs	0.000	0.997	0.003
D55-D59 Haemolytic anaemias	0.000	0.997	0.003
M88.90 Paget's disease of bone, unspecified (Multiple sites)	0.000	0.997	0.003
D84.1 Defects in the complement system	0.000	0.997	0.003
N36.3 Prolapsed urethral mucosa	0.000	0.997	0.003
M54.64 Pain in thoracic spine (Thoracic region)	0.003	0.997	0.000
K12.0 Recurrent oral aphthae	0.000	0.997	0.003
D86.3 Sarcoidosis of skin	0.000	0.997	0.003
M05.2 Rheumatoid vasculitis	0.000	0.997	0.003
R49.2 Hypernasality and hyponasality	0.000	0.997	0.003
B17.1 Acute hepatitis C	0.003	0.997	0.000
I63.3 Cerebral infarction due to thrombosis of cerebral arteries	0.000	0.997	0.003
B15 Acute hepatitis A	0.003	0.997	0.000
M13.93 Arthritis, unspecified (Forearm)	0.003	0.997	0.000
A87.9 Viral meningitis, unspecified	0.000	0.997	0.003
B17 Other acute viral hepatitis	0.003	0.997	0.000
K12 Stomatitis and related lesions	0.000	0.997	0.003
B15.9 Hepatitis A without hepatic coma	0.003	0.997	0.000
D22.1 Melanocytic naevi of eyelid, including canthus	0.000	0.997	0.003
M05.1 Rheumatoid lung disease	0.000	0.997	0.003
R52.9 Pain, unspecified	0.000	0.997	0.003
M05.3 Rheumatoid arthritis with involvement of other organs and systems	0.000	0.997	0.003
M05.0 Felty's syndrome	0.000	0.997	0.003
M05.8 Other seropositive rheumatoid arthritis	0.000	0.997	0.003
Y84.6 Urinary catheterisation	0.003	0.997	0.000
G80 Infantile cerebral palsy	0.000	0.997	0.003
Y83-Y84 Surgical and other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure	0.003	0.997	0.000
D60.9 Acquired pure red cell aplasia, unspecified	0.000	0.997	0.003
D86.9 Sarcoidosis, unspecified	0.000	0.997	0.003
B19 Unspecified viral hepatitis	0.003	0.997	0.000
Z22.5 Carrier of viral hepatitis	0.003	0.997	0.000
Q24 Other congenital malformations of heart	0.003	0.997	0.000
D60.8 Other acquired pure red cell aplasias	0.000	0.997	0.003
D60.1 Transient acquired pure red cell aplasia	0.000	0.997	0.003
D60.0 Chronic acquired pure red cell aplasia	0.000	0.997	0.003
H20.9 Iridocyclitis, unspecified	0.000	0.997	0.003
I63.2 Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries	0.000	0.997	0.003
Z99.3 Dependence on wheelchair	0.000	0.997	0.003
M05.29 Rheumatoid vasculitis (Site unspecified)	0.000	0.997	0.003
S92.00 Fracture of calcaneus (closed)	0.003	0.997	0.000
T45.5 Anticoagulants	0.000	0.997	0.003
I84.8 Unspecified haemorrhoids with other complications	0.003	0.997	0.000
D55 Anaemia due to enzyme disorders	0.000	0.997	0.002
T45 Poisoning by primarily systemic and haematological agents, not elsewhere classified	0.000	0.997	0.003
K86.8 Other specified diseases of pancreas	0.003	0.997	0.000
T81.2 Accidental puncture and laceration during a procedure, not elsewhere classified	0.000	0.997	0.003
D89.2 Hypergammaglobulinaemia, unspecified	0.000	0.997	0.003
M50.3 Other cervical disk degeneration	0.000	0.997	0.003
M13.95 Arthritis, unspecified (Pelvic region and thigh)	0.000	0.997	0.003
B16 Acute hepatitis B	0.002	0.997	0.000
M05.28 Rheumatoid vasculitis (Other)	0.000	0.997	0.002
M05.27 Rheumatoid vasculitis (Ankle and foot)	0.000	0.997	0.002
M05.26 Rheumatoid vasculitis (Lower leg)	0.000	0.997	0.002
M05.25 Rheumatoid vasculitis (Pelvic region and thigh)	0.000	0.997	0.002
M05.24 Rheumatoid vasculitis (Hand)	0.000	0.997	0.002
M05.23 Rheumatoid vasculitis (Forearm)	0.000	0.997	0.002
M05.22 Rheumatoid vasculitis (Upper arm)	0.000	0.997	0.002
M05.21 Rheumatoid vasculitis (Shoulder region)	0.000	0.997	0.002
M05.20 Rheumatoid vasculitis (Multiple sites)	0.000	0.997	0.002
B15.0 Hepatitis A with hepatic coma	0.002	0.997	0.000
T45.1 Antineoplastic and immunosuppressive drugs	0.000	0.998	0.002
D61 Other aplastic anaemias	0.000	0.998	0.002
B17.0 Acute delta-(super) infection of hepatitis B carrier	0.002	0.998	0.000
M05.19 Rheumatoid lung disease (Site unspecified)	0.000	0.998	0.002
M05.18 Rheumatoid lung disease (Other)	0.000	0.998	0.002
M05.17 Rheumatoid lung disease (Ankle and foot)	0.000	0.998	0.002
M05.16 Rheumatoid lung disease (Lower leg)	0.000	0.998	0.002
M05.15 Rheumatoid lung disease (Pelvic region and thigh)	0.000	0.998	0.002
M05.14 Rheumatoid lung disease (Hand)	0.000	0.998	0.002
M05.13 Rheumatoid lung disease (Forearm)	0.000	0.998	0.002
M05.12 Rheumatoid lung disease (Upper arm)	0.000	0.998	0.002
M05.11 Rheumatoid lung disease (Shoulder region)	0.000	0.998	0.002
M05.10 Rheumatoid lung disease (Multiple sites)	0.000	0.998	0.002
B17.9 Acute viral hepatitis, unspecified	0.002	0.998	0.000
K12.3 Oral mucositis (ulcerative)	0.000	0.998	0.002
M05.09 Felty's syndrome (Site unspecified)	0.000	0.998	0.002
M05.08 Felty's syndrome (Other)	0.000	0.998	0.002
M05.07 Felty's syndrome (Ankle and foot)	0.000	0.998	0.002
M05.06 Felty's syndrome (Lower leg)	0.000	0.998	0.002
M05.05 Felty's syndrome (Pelvic region and thigh)	0.000	0.998	0.002
M05.04 Felty's syndrome (Hand)	0.000	0.998	0.002
M05.03 Felty's syndrome (Forearm)	0.000	0.998	0.002
M05.02 Felty's syndrome (Upper arm)	0.000	0.998	0.002
M05.01 Felty's syndrome (Shoulder region)	0.000	0.998	0.002
M05.00 Felty's syndrome (Multiple sites)	0.000	0.998	0.002
M05.39 Rheumatoid arthritis with involvement of other organs and systems (Site unspecified)	0.000	0.998	0.002
M05.38 Rheumatoid arthritis with involvement of other organs and systems (Other)	0.000	0.998	0.002
M05.37 Rheumatoid arthritis with involvement of other organs and systems (Ankle and foot)	0.000	0.998	0.002
M05.36 Rheumatoid arthritis with involvement of other organs and systems (Lower leg)	0.000	0.998	0.002
M05.35 Rheumatoid arthritis with involvement of other organs and systems (Pelvic region and thigh)	0.000	0.998	0.002
M05.34 Rheumatoid arthritis with involvement of other organs and systems (Hand)	0.000	0.998	0.002
M05.33 Rheumatoid arthritis with involvement of other organs and systems (Forearm)	0.000	0.998	0.002
M05.32 Rheumatoid arthritis with involvement of other organs and systems (Upper arm)	0.000	0.998	0.002
M05.31 Rheumatoid arthritis with involvement of other organs and systems (Shoulder region)	0.000	0.998	0.002
M05.30 Rheumatoid arthritis with involvement of other organs and systems (Multiple sites)	0.000	0.998	0.002
M05.80 Other seropositive rheumatoid arthritis (Multiple sites)	0.000	0.998	0.002
G24.9 Dystonia, unspecified	0.002	0.998	0.000
G80.8 Other infantile cerebral palsy	0.000	0.998	0.002
Q24.0 Dextrocardia	0.002	0.998	0.000
C56 Malignant neoplasm of ovary	0.000	0.998	0.002
B19.9 Unspecified viral hepatitis without coma	0.002	0.998	0.000
Q24.5 Malformation of coronary vessels	0.002	0.998	0.000
M05.88 Other seropositive rheumatoid arthritis (Other)	0.000	0.998	0.002
M05.87 Other seropositive rheumatoid arthritis (Ankle and foot)	0.000	0.998	0.002
M05.86 Other seropositive rheumatoid arthritis (Lower leg)	0.000	0.998	0.002
M05.85 Other seropositive rheumatoid arthritis (Pelvic region and thigh)	0.000	0.998	0.002
M05.84 Other seropositive rheumatoid arthritis (Hand)	0.000	0.998	0.002
M05.83 Other seropositive rheumatoid arthritis (Forearm)	0.000	0.998	0.002
M05.82 Other seropositive rheumatoid arthritis (Upper arm)	0.000	0.998	0.002
M05.81 Other seropositive rheumatoid arthritis (Shoulder region)	0.000	0.998	0.002
G80.1 Spastic diplegia	0.000	0.998	0.002
G80.0 Spastic cerebral palsy	0.000	0.998	0.002
D57 Sickle-cell disorders	0.000	0.998	0.002
G80.4 Ataxic cerebral palsy	0.000	0.998	0.002
G80.3 Dyskinetic cerebral palsy	0.000	0.998	0.002
B17.2 Acute hepatitis E	0.002	0.998	0.000
T45.2 Vitamins, not elsewhere classified	0.000	0.998	0.002
Q24.6 Congenital heart block	0.002	0.998	0.000
B19.0 Unspecified viral hepatitis with coma	0.002	0.998	0.000
D58 Other hereditary haemolytic anaemias	0.000	0.998	0.002
Q24.4 Congenital subaortic stenosis	0.002	0.998	0.000
Q24.3 Pulmonary infundibular stenosis	0.002	0.998	0.000
Q24.2 Cor triatriatum	0.002	0.998	0.000
Q24.1 Levocardia	0.002	0.998	0.000
M05.89 Other seropositive rheumatoid arthritis (Site unspecified)	0.000	0.998	0.002
H59.9 Postprocedural disorder of eye and adnexa, unspecified	0.000	0.998	0.002
M62.85 Other specified disorders of muscle (Pelvic region and thigh)	0.000	0.998	0.002
B17.8 Other specified acute viral hepatitis	0.002	0.998	0.000
D55.9 Anaemia due to enzyme disorder, unspecified	0.000	0.998	0.002
D55.8 Other anaemias due to enzyme disorders	0.000	0.998	0.002
D55.3 Anaemia due to disorders of nucleotide metabolism	0.000	0.998	0.002
D55.2 Anaemia due to disorders of glycolytic enzymes	0.000	0.998	0.002
D55.1 Anaemia due to other disorders of glutathione metabolism	0.000	0.998	0.002
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency	0.000	0.998	0.002
F45.8 Other somatoform disorders	0.000	0.998	0.002
Q78.0 Osteogenesis imperfecta	0.002	0.998	0.000
D56 Thalassaemia	0.001	0.998	0.002
D86.0 Sarcoidosis of lung	0.000	0.998	0.002
T45.9 Primarily systemic and haematological agent, unspecified	0.000	0.998	0.002
T45.8 Other primarily systemic and haematological agents	0.000	0.998	0.002
T45.7 Anticoagulant antagonists, vitamin K and other coagulants	0.000	0.998	0.002
T45.6 Fibrinolysis-affecting drugs	0.000	0.998	0.002
T45.4 Iron and its compounds	0.000	0.998	0.002
T45.3 Enzymes, not elsewhere classified	0.000	0.998	0.002
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
K13.0 Diseases of lips	0.000	0.998	0.002
V18.2 Unspecified pedal cyclist injured in nontraffic accident	0.000	0.998	0.002
D61.0 Constitutional aplastic anaemia	0.000	0.998	0.002
Q66.7 Pes cavus	0.002	0.998	0.000
B16.2 Acute hepatitis B without delta-agent with hepatic coma	0.002	0.998	0.000
B16.1 Acute hepatitis B with delta-agent (coinfection) without hepatic coma	0.002	0.998	0.000
B16.0 Acute hepatitis B with delta-agent (coinfection) with hepatic coma	0.002	0.998	0.000
D59 Acquired haemolytic anaemia	0.000	0.998	0.002
D61.1 Drug-induced aplastic anaemia	0.000	0.998	0.002
Q61.0 Congenital single renal cyst	0.000	0.998	0.002
Z13.5 Special screening examination for eye and ear disorders	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q39.4 Oesophageal web	0.002	0.998	0.000
F05.0 Delirium not superimposed on dementia, so described	0.000	0.998	0.002
D61.8 Other specified aplastic anaemias	0.000	0.998	0.002
D61.3 Idiopathic aplastic anaemia	0.000	0.998	0.002
D61.2 Aplastic anaemia due to other external agents	0.000	0.998	0.002
Q43.8 Other specified congenital malformations of intestine	0.002	0.998	0.000
M79.28 Neuralgia and neuritis, unspecified (Other)	0.000	0.998	0.002
O68.9 Labour and delivery complicated by foetal stress, unspecified	0.000	0.998	0.002
G24.3 Spasmodic torticollis	0.002	0.998	0.000
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
T94.1 Sequelae of injuries, not specified by body region	0.000	0.998	0.002
A87 Viral meningitis	0.000	0.998	0.002
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
D57.8 Other sickle-cell disorders	0.000	0.998	0.002
D57.2 Double heterozygous sickling disorders	0.000	0.998	0.002
D57.0 Sickle-cell anaemia with crisis	0.000	0.998	0.002
H58.8 Visual disturbances in diseases classified elsewhere	0.000	0.998	0.002
D70-D77 Other diseases of blood and blood-forming organs	0.000	0.998	0.002
B16.9 Acute hepatitis B without delta-agent and without hepatic coma	0.002	0.998	0.000
G24.5 Blepharospasm	0.002	0.998	0.000
N99.4 Postprocedural pelvic peritoneal adhesions	0.000	0.998	0.002
G24 Dystonia	0.002	0.998	0.000
Q27.3 Peripheral arteriovenous malformation	0.002	0.998	0.000
D58.8 Other specified hereditary haemolytic anaemias	0.000	0.998	0.002
D58.1 Hereditary elliptocytosis	0.000	0.998	0.002
G80.2 Infantile hemiplegia	0.000	0.998	0.002
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
K56.1 Intussusception	0.000	0.998	0.002
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
H02.1 Ectropion of eyelid	0.000	0.998	0.002
Q39.9 Congenital malformation of oesophagus, unspecified	0.002	0.998	0.000
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
G24.0 Drug-induced dystonia	0.002	0.998	0.000
J86.9 Pyothorax without fistula	0.000	0.998	0.002
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
D56.9 Thalassaemia, unspecified	0.001	0.998	0.001
D56.8 Other thalassaemias	0.001	0.998	0.001
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]	0.001	0.998	0.001
D56.2 Delta-beta thalassaemia	0.001	0.998	0.001
D56.0 Alpha thalassaemia	0.001	0.998	0.001
D57.3 Sickle-cell trait	0.001	0.998	0.001
Q43 Other congenital malformations of intestine	0.002	0.998	0.000
C51.9 Vulva, unspecified	0.002	0.998	0.000
O00.9 Ectopic pregnancy, unspecified	0.000	0.998	0.002
Q39.8 Other congenital malformations of oesophagus	0.002	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.002	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.002	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.002	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.002	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.002	0.998	0.000
D57.1 Sickle-cell anaemia without crisis	0.001	0.998	0.001
D58.2 Other haemoglobinopathies	0.000	0.998	0.001
D58.0 Hereditary spherocytosis	0.000	0.998	0.002
Q78.2 Osteopetrosis	0.002	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
S22.40 Multiple fractures of ribs (closed)	0.000	0.998	0.002
D59.9 Acquired haemolytic anaemia, unspecified	0.000	0.998	0.002
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.000	0.998	0.002
M62.88 Other specified disorders of muscle (Other)	0.000	0.998	0.002
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
D59.3 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
J84.1 Other interstitial pulmonary diseases with fibrosis	0.000	0.998	0.002
N82.3 Fistula of vagina to large intestine	0.000	0.998	0.002
Q38.8 Other congenital malformations of pharynx	0.002	0.998	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
L98.9 Disorder of skin and subcutaneous tissue, unspecified	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
N42.8 Other specified disorders of prostate	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
Q79.6 Ehlers-Danlos syndrome	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
N82.4 Other female intestinal-genital tract fistulae	0.000	0.998	0.002
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q79.0 Congenital diaphragmatic hernia	0.002	0.998	0.000
D64 Other anaemias	0.000	0.998	0.002
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
G24.1 Idiopathic familial dystonia	0.002	0.998	0.000
N82.9 Female genital tract fistula, unspecified	0.000	0.998	0.002
N97.9 Female infertility, unspecified	0.000	0.998	0.002
S52.60 Fracture of lower end of both ulna and radius (closed)	0.000	0.998	0.002
A16.9 Respiratory tuberculosis unspecified, without mention of bacteriological or histological confirmation	0.000	0.998	0.002
A87.8 Other viral meningitis	0.000	0.998	0.002
A87.2 Lymphocytic choriomeningitis	0.000	0.998	0.002
A87.1 Adenoviral meningitis	0.000	0.998	0.002
A87.0 Enteroviral meningitis	0.000	0.998	0.002
Q28.0 Arteriovenous malformation of precerebral vessels	0.002	0.998	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.002	0.998	0.000
Q78.8 Other specified osteochondrodysplasias	0.002	0.998	0.000
Q78.6 Multiple congenital exostoses	0.002	0.998	0.000
Q78.5 Metaphyseal dysplasia	0.002	0.998	0.000
Q78.4 Enchondromatosis	0.002	0.998	0.000
Q78.3 Progressive diaphyseal dysplasia	0.002	0.998	0.000
Q78.1 Polyostotic fibrous dysplasia	0.002	0.998	0.000
R25.8 Other and unspecified abnormal involuntary movements	0.000	0.998	0.002
Z01.9 Special examination, unspecified	0.002	0.998	0.000
C41.9 Bone and articular cartilage, unspecified	0.002	0.998	0.000
D59.4 Other nonautoimmune haemolytic anaemias	0.000	0.998	0.001
H60.3 Other infective otitis externa	0.000	0.998	0.002
Q05.9 Spina bifida, unspecified	0.002	0.998	0.000
Q43.1 Hirschsprung's disease	0.002	0.998	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.002	0.998	0.000
M62.80 Other specified disorders of muscle (Multiple sites)	0.000	0.998	0.002
D56.3 Thalassaemia trait	0.001	0.998	0.001
D76.3 Other histiocytosis syndromes	0.000	0.998	0.002
G24.4 Idiopathic orofacial dystonia	0.002	0.998	0.000
G24.2 Idiopathic nonfamilial dystonia	0.002	0.998	0.000
Z75.4 Unavailability and inaccessibility of other helping agencies	0.002	0.998	0.000
D74 Methaemoglobinaemia	0.000	0.998	0.002
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere	0.000	0.998	0.002
D71 Functional disorders of polymorphonuclear neutrophils	0.000	0.998	0.002
Q66 Congenital deformities of feet	0.002	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
H59 Postprocedural disorders of eye and adnexa, not elsewhere classified	0.000	0.998	0.002
Q26 Congenital malformations of great veins	0.002	0.998	0.000
D56.1 Beta thalassaemia	0.001	0.998	0.001
D58.9 Hereditary haemolytic anaemia, unspecified	0.000	0.998	0.001
M14.6 Neuropathic arthropathy	0.000	0.998	0.002
Q24.9 Congenital malformation of the heart, unspecified	0.001	0.998	0.000
Q44.4 Choledochal cyst	0.001	0.998	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.001	0.998	0.000
Q44.2 Atresia of bile ducts	0.001	0.998	0.000
Q44.1 Other congenital malformations of gallbladder	0.001	0.998	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.001	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.001	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.001	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
F05.9 Delirium, unspecified	0.000	0.998	0.002
Q27.4 Congenital phlebectasia	0.001	0.998	0.000
Q27.2 Other congenital malformations of renal artery	0.001	0.998	0.000
Q27.1 Congenital renal artery stenosis	0.001	0.998	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	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
Q45.9 Congenital malformation of digestive system, unspecified	0.001	0.998	0.000
Q66.0 Talipes equinovarus	0.002	0.998	0.000
R90.8 Other abnormal findings on diagnostic imaging of central nervous system	0.000	0.998	0.002
R47-R49 Symptoms and signs involving speech and voice	0.000	0.998	0.002
G93.8 Other specified disorders of brain	0.000	0.998	0.002
N99.3 Prolapse of vaginal vault after hysterectomy	0.000	0.998	0.002
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
Q43.2 Other congenital functional disorders of colon	0.001	0.998	0.000
H02 Other disorders of eyelid	0.000	0.998	0.002
Q70 Syndactyly	0.002	0.998	0.000
H04.9 Disorder of lachrymal system, unspecified	0.000	0.998	0.002
K91.9 Postprocedural disorder of digestive system, unspecified	0.000	0.998	0.002
T87.4 Infection of amputation stump	0.002	0.998	0.000
S27.20 Traumatic haemopneumothorax (without open wound into thoracic cavity)	0.000	0.998	0.002
D17.6 Benign lipomatous neoplasm of spermatic cord	0.000	0.998	0.002
D76.2 Haemophagocytic syndrome, infection-associated	0.000	0.998	0.001
D76.1 Haemophagocytic lymphohistiocytosis	0.000	0.998	0.001
D76.0 Langerhans' cell histiocytosis, not elsewhere classified	0.000	0.998	0.001
L04.2 Acute lymphadenitis of upper limb	0.002	0.998	0.000
M54.6 Pain in thoracic spine	0.002	0.998	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.001	0.998	0.000
Q79.5 Other congenital malformations of abdominal wall	0.001	0.998	0.000
Q79.4 Prune belly syndrome	0.001	0.998	0.000
Q79.3 Gastroschisis	0.001	0.998	0.000
Q79.2 Exomphalos	0.001	0.998	0.000
Q79.1 Other congenital malformations of diaphragm	0.001	0.998	0.000
Y85.0 Sequelae of motor-vehicle accident	0.000	0.998	0.002
H58 Other disorders of eye and adnexa in diseases classified elsewhere	0.000	0.998	0.002
N82 Fistulae involving female genital tract	0.000	0.998	0.002
N82.0 Vesicovaginal fistula	0.000	0.998	0.002
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.998	0.000
Q43.3 Congenital malformations of intestinal fixation	0.001	0.998	0.000

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

The full results table can be downloaded from this page.

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

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

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

Variant-specific associations