TreeWAS – Variant ID: rs9506942

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
D68.8 Other specified coagulation defects	0.061	0.939	0.000
D68.9 Coagulation defect, unspecified	0.048	0.952	0.000
D68 Other coagulation defects	0.047	0.953	0.000
D68.1 Hereditary factor XI deficiency	0.035	0.965	0.000
D68.6 Other Thrombophilia	0.033	0.967	0.000
D68.4 Acquired coagulation factor deficiency	0.033	0.967	0.000
D68.0 Von Willebrand's disease	0.032	0.968	0.000
D68.3 Haemorrhagic disorder due to circulating anticoagulants	0.031	0.969	0.000
D68.5 Primary Thrombophilia	0.029	0.971	0.000
D68.2 Hereditary deficiency of other clotting factors	0.024	0.976	0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.019	0.981	0.000
N73.9 Female pelvic inflammatory disease, unspecified	0.018	0.982	0.000
D66 Hereditary factor VIII deficiency	0.017	0.983	0.000
D67 Hereditary factor IX deficiency	0.015	0.985	0.000
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.014	0.986	0.000
G51.0 Bell's palsy	0.000	0.988	0.012
D10.3 Other and unspecified parts of mouth	0.010	0.990	0.000
D10 Benign neoplasm of mouth and pharynx	0.008	0.992	0.000
D10.6 Nasopharynx	0.007	0.993	0.000
D10.0 Lip	0.007	0.993	0.000
K56.5 Intestinal adhesions [bands] with obstruction	0.000	0.993	0.007
D10.5 Other parts of oropharynx	0.007	0.993	0.000
M70.65 Trochanteric bursitis-Pelvic/Thigh	0.000	0.993	0.007
D10.9 Pharynx, unspecified	0.007	0.993	0.000
C34.1 Upper lobe, bronchus or lung	0.000	0.994	0.006
G51 Facial nerve disorders	0.000	0.994	0.006
G51.3 Clonic hemifacial spasm	0.000	0.994	0.006
D10.7 Hypopharynx	0.006	0.994	0.000
D10.2 Floor of mouth	0.006	0.994	0.000
D10.4 Tonsil	0.006	0.994	0.000
D10.1 Tongue	0.006	0.994	0.000
Z87.4 Personal history of diseases of the genito-urinary system	0.000	0.994	0.006
H40.8 Other glaucoma	0.005	0.994	0.000
N73 Other female pelvic inflammatory diseases	0.005	0.995	0.000
K62.6 Ulcer of anus and rectum	0.000	0.995	0.005
T80.2 Infections following infusion, transfusion and therapeutic injection	0.000	0.995	0.005
Q23.1 Congenital insufficiency of aortic valve	0.005	0.995	0.000
D69 Purpura and other haemorrhagic conditions	0.005	0.995	0.000
G51.4 Facial myokymia	0.000	0.995	0.005
G51.2 Melkersson's syndrome	0.000	0.995	0.005
G51.1 Geniculate ganglionitis	0.000	0.995	0.005
M48.07 Spinal stenosis (Lumbosacral region)	0.005	0.995	0.000
N73.1 Chronic parametritis and pelvic cellulitis	0.005	0.995	0.000
D86 Sarcoidosis	0.005	0.995	0.000
N73.0 Acute parametritis and pelvic cellulitis	0.004	0.996	0.000
D86.8 Sarcoidosis of other and combined sites	0.004	0.996	0.000
N73.8 Other specified female pelvic inflammatory diseases	0.004	0.996	0.000
D86.1 Sarcoidosis of lymph nodes	0.004	0.996	0.000
G51.9 Disorder of facial nerve, unspecified	0.000	0.996	0.004
D69.3 Idiopathic thrombocytopenic purpura	0.004	0.996	0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.004	0.996	0.000
N73.4 Female chronic pelvic peritonitis	0.004	0.996	0.000
N73.3 Female acute pelvic peritonitis	0.004	0.996	0.000
N73.2 Unspecified parametritis and pelvic cellulitis	0.004	0.996	0.000
D86.3 Sarcoidosis of skin	0.004	0.996	0.000
E89.0 Postprocedural hypothyroidism	0.004	0.996	0.000
G51.8 Other disorders of facial nerve	0.000	0.996	0.004
D69.1 Qualitative platelet defects	0.004	0.996	0.000
N73.5 Female pelvic peritonitis, unspecified	0.004	0.996	0.000
D69.2 Other nonthrombocytopenic purpura	0.004	0.996	0.000
D69.0 Allergic purpura	0.004	0.996	0.000
D86.9 Sarcoidosis, unspecified	0.004	0.996	0.000
D69.8 Other specified haemorrhagic conditions	0.004	0.996	0.000
E06.3 Autoimmune thyroiditis	0.004	0.996	0.000
D80-D89 Certain disorders involving the immune mechanism	0.004	0.996	0.000
H16.0 Corneal ulcer	0.000	0.996	0.004
M70.6 Trochanteric bursitis	0.000	0.996	0.004
N13.5 Kinking and stricture of ureter without hydronephrosis	0.004	0.996	0.000
I84.3 External thrombosed haemorrhoids	0.000	0.997	0.003
Q23 Congenital malformations of aortic and mitral valves	0.003	0.997	0.000
D69.9 Haemorrhagic condition, unspecified	0.003	0.997	0.000
F45.8 Other somatoform disorders	0.000	0.997	0.003
D82 Immunodeficiency associated with other major defects	0.003	0.997	0.000
M20.5 Other deformities of toe(s) (acquired)	0.000	0.997	0.003
K45.8 Other specified abdominal hernia without obstruction or gangrene	0.003	0.997	0.000
T80 Complications following infusion, transfusion and therapeutic injection	0.000	0.997	0.003
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.003	0.997	0.000
H65.2 Chronic serous otitis media	0.000	0.997	0.003
Q23.0 Congenital stenosis of aortic valve	0.003	0.997	0.000
D83 Common variable immunodeficiency	0.003	0.997	0.000
D86.0 Sarcoidosis of lung	0.003	0.997	0.000
D82.1 Di George's syndrome	0.003	0.997	0.000
Z92.6 Personal history of chemotherapy for neoplastic disease	0.000	0.997	0.003
D81 Combined immunodeficiencies	0.003	0.997	0.000
T80.8 Other complications following infusion, transfusion and therapeutic injection	0.000	0.997	0.003
D69.4 Other primary thrombocytopenia	0.003	0.997	0.000
M70.68 Trochanteric bursitis-Other	0.000	0.997	0.003
M70.67 Trochanteric bursitis-Ankle/Foot	0.000	0.997	0.003
M70.66 Trochanteric bursitis-Lower Leg	0.000	0.997	0.003
M70.64 Trochanteric bursitis-Hand	0.000	0.997	0.003
M70.63 Trochanteric bursitis-Forearm	0.000	0.997	0.003
M70.62 Trochanteric bursitis-Upper arm	0.000	0.997	0.003
M70.61 Trochanteric bursitis-Shldr region	0.000	0.997	0.003
M70.60 Trochanteric bursitis-Mult sites	0.000	0.997	0.003
T80.1 Vascular complications following infusion, transfusion and therapeutic injection	0.000	0.997	0.003
I73.0 Raynaud's syndrome	0.003	0.997	0.000
X62.9 Unspecified place	0.003	0.997	0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.003	0.997	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.003	0.997	0.000
Q23.4 Hypoplastic left heart syndrome	0.003	0.997	0.000
Q23.3 Congenital mitral insufficiency	0.003	0.997	0.000
Q23.2 Congenital mitral stenosis	0.003	0.997	0.000
M70.69 Trochanteric bursitis-Site unspec	0.000	0.997	0.003
M79.69 Pain in limb (Site unspecified)	0.003	0.997	0.000
D80 Immunodeficiency with predominantly antibody defects	0.003	0.997	0.000
G55.3 Nerve root and plexus compressions in other dorsopathies	0.003	0.997	0.000
D82.9 Immunodeficiency associated with major defect, unspecified	0.002	0.997	0.000
D82.8 Immunodeficiency associated with other specified major defects	0.002	0.997	0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.002	0.997	0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.002	0.997	0.000
D82.2 Immunodeficiency with short-limbed stature	0.002	0.997	0.000
D82.0 Wiskott-Aldrich syndrome	0.002	0.997	0.000
D84 Other immunodeficiencies	0.003	0.997	0.000
Z01.6 Radiological examination, not elsewhere classified	0.000	0.997	0.003
D83.9 Common variable immunodeficiency, unspecified	0.002	0.997	0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.003	0.997	0.000
T80.6 Other serum reactions	0.000	0.997	0.002
T80.5 Anaphylactic shock due to serum	0.000	0.997	0.002
T80.4 Rh incompatibility reaction	0.000	0.997	0.002
T80.3 ABO incompatibility reaction	0.000	0.997	0.002
T80.0 Air embolism following infusion, transfusion and therapeutic injection	0.000	0.997	0.002
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
G25.0 Essential tremor	0.002	0.998	0.000
D55-D59 Haemolytic anaemias	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
E89 Postprocedural endocrine and metabolic disorders, not elsewhere classified	0.002	0.998	0.000
H16 Keratitis	0.000	0.998	0.002
D37.7 Other digestive organs	0.002	0.998	0.000
E89.8 Other postprocedural endocrine and metabolic disorders	0.002	0.998	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.002	0.998	0.000
Y43.3 Other antineoplastic drugs	0.000	0.998	0.002
D89.0 Polyclonal hypergammaglobulinaemia	0.002	0.998	0.000
G12.2 Motor neuron disease	0.000	0.998	0.002
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.002	0.998	0.000
T83.8 Other complications of genito-urinary prosthetic devices, implants and grafts	0.002	0.998	0.000
D69.5 Secondary thrombocytopenia	0.002	0.998	0.000
D23.9 Skin, unspecified	0.002	0.998	0.000
H16.1 Other superficial keratitis without conjunctivitis	0.000	0.998	0.002
K07.3 Anomalies of tooth position	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
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.002	0.998	0.000
D80.0 Hereditary hypogammaglobulinaemia	0.002	0.998	0.000
V89.2 Person injured in unspecified motor-vehicle accident, traffic	0.000	0.998	0.002
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.002	0.998	0.000
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.002	0.998	0.000
E89.3 Postprocedural hypopituitarism	0.002	0.998	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.002	0.998	0.000
T80.9 Unspecified complication following infusion, transfusion and therapeutic injection	0.000	0.998	0.002
D43.0 Brain, supratentorial	0.002	0.998	0.000
D80.1 Nonfamilial hypogammaglobulinaemia	0.002	0.998	0.000
D89.3 Immune reconstitution syndrome	0.002	0.998	0.000
D84.9 Immunodeficiency, unspecified	0.002	0.998	0.000
E89.1 Postprocedural hypoinsulinaemia	0.002	0.998	0.000
I61.4 Intracerebral haemorrhage in cerebellum	0.002	0.998	0.000
D84.1 Defects in the complement system	0.002	0.998	0.000
H16.3 Interstitial and deep keratitis	0.000	0.998	0.002
D58 Other hereditary haemolytic anaemias	0.002	0.998	0.000
H16.8 Other keratitis	0.000	0.998	0.002
G04.9 Encephalitis, myelitis and encephalomyelitis, unspecified	0.002	0.998	0.000
D59 Acquired haemolytic anaemia	0.002	0.998	0.000
D84.8 Other specified immunodeficiencies	0.002	0.998	0.000
T81.3 Disruption of operation wound, not elsewhere classified	0.002	0.998	0.000
D57 Sickle-cell disorders	0.002	0.998	0.000
D55 Anaemia due to enzyme disorders	0.002	0.998	0.000
M81.90 Osteoporosis, unspecified (Multiple sites)	0.000	0.998	0.002
E89.9 Postprocedural endocrine and metabolic disorder, unspecified	0.002	0.998	0.000
E89.5 Postprocedural testicular hypofunction	0.002	0.998	0.000
H16.2 Keratoconjunctivitis	0.000	0.998	0.002
C15.3 Upper third of oesophagus	0.002	0.998	0.000
S00.3 Superficial injury of nose	0.002	0.998	0.000
Z01.4 Gynaecological examination (general)(routine)	0.000	0.998	0.002
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.002	0.998	0.000
D59.0 Drug-induced autoimmune haemolytic anaemia	0.002	0.998	0.000
E89.6 Postprocedural adrenocortical(-medullary) hypofunction	0.002	0.998	0.000
H16.4 Corneal neovascularisation	0.000	0.998	0.002
K90.9 Intestinal malabsorption, unspecified	0.000	0.998	0.002
M43.02 Spondylolysis (Cervical region)	0.000	0.998	0.002
E06.9 Thyroiditis, unspecified	0.002	0.998	0.000
D58.0 Hereditary spherocytosis	0.002	0.998	0.000
D89.1 Cryoglobulinaemia	0.002	0.998	0.000
H16.9 Keratitis, unspecified	0.000	0.998	0.002
I61.1 Intracerebral haemorrhage in hemisphere, cortical	0.002	0.998	0.000
W44.0 Home	0.002	0.998	0.000
E06 Thyroiditis	0.002	0.998	0.000
D58.8 Other specified hereditary haemolytic anaemias	0.002	0.998	0.000
D58.1 Hereditary elliptocytosis	0.002	0.998	0.000
E89.4 Postprocedural ovarian failure	0.002	0.998	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.002	0.998	0.000
M80.10 Postoophorectomy osteoporosis with pathological fracture (Multiple sites)	0.002	0.998	0.000
D58.9 Hereditary haemolytic anaemia, unspecified	0.002	0.998	0.000
D58.2 Other haemoglobinopathies	0.002	0.998	0.000
E89.2 Postprocedural hypoparathyroidism	0.002	0.998	0.000
O99.4 Diseases of the circulatory system complicating pregnancy, childbirth and the puerperium	0.002	0.998	0.000
D59.8 Other acquired haemolytic anaemias	0.002	0.998	0.000
D59.6 Haemoglobinuria due to haemolysis from other external causes	0.002	0.998	0.000
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]	0.002	0.998	0.000
D59.4 Other nonautoimmune haemolytic anaemias	0.002	0.998	0.000
D59.3 Haemolytic-uraemic syndrome	0.002	0.998	0.000
D59.2 Drug-induced nonautoimmune haemolytic anaemia	0.002	0.998	0.000
D55.9 Anaemia due to enzyme disorder, unspecified	0.001	0.998	0.000
D55.8 Other anaemias due to enzyme disorders	0.001	0.998	0.000
D55.3 Anaemia due to disorders of nucleotide metabolism	0.001	0.998	0.000
D55.2 Anaemia due to disorders of glycolytic enzymes	0.001	0.998	0.000
D55.1 Anaemia due to other disorders of glutathione metabolism	0.001	0.998	0.000
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency	0.001	0.998	0.000
D57.8 Other sickle-cell disorders	0.001	0.998	0.000
D57.3 Sickle-cell trait	0.001	0.998	0.000
D57.2 Double heterozygous sickling disorders	0.001	0.998	0.000
D57.1 Sickle-cell anaemia without crisis	0.001	0.998	0.000
D57.0 Sickle-cell anaemia with crisis	0.001	0.998	0.000
D56 Thalassaemia	0.001	0.998	0.000
H10.9 Conjunctivitis, unspecified	0.002	0.998	0.000
Z11.2 Special screening examination for other bacterial diseases	0.000	0.998	0.002
F45 Somatoform disorders	0.000	0.998	0.002
T83.4 Mechanical complication of other prosthetic devices, implants and grafts in genital tract	0.002	0.998	0.000
F45.4 Persistent somatoform pain disorder	0.000	0.998	0.002
M70.56 Other bursitis of knee-Lower Leg	0.000	0.998	0.002
D59.1 Other autoimmune haemolytic anaemias	0.002	0.998	0.000
G72.9 Myopathy, unspecified	0.000	0.998	0.002
V89.9 Person injured in unspecified vehicle accident	0.000	0.998	0.002
G25.8 Other specified extrapyramidal and movement disorders	0.002	0.998	0.000
X62 Intentional self-poisoning by and exposure to narcotics and psychodysleptics [hallucinogens], not elsewhere classified	0.002	0.998	0.000
C49.3 Connective and soft tissue of thorax	0.000	0.998	0.002
D59.9 Acquired haemolytic anaemia, unspecified	0.001	0.998	0.000
M70.5 Other bursitis of knee	0.000	0.998	0.001
M43.09 Spondylolysis (Site unspecified)	0.000	0.998	0.002
V89 Motor- or nonmotor-vehicle accident, type of vehicle unspecified	0.000	0.998	0.002
M94.89 Other specified disorders of cartilage (Site unspecified)	0.002	0.998	0.000
C16.9 Stomach, unspecified	0.000	0.998	0.002
E06.4 Drug-induced thyroiditis	0.001	0.998	0.000
E06.2 Chronic thyroiditis with transient thyrotoxicosis	0.001	0.998	0.000
E06.0 Acute thyroiditis	0.001	0.998	0.000
F45.0 Somatisation disorder	0.000	0.998	0.001
N95.3 States associated with artificial menopause	0.000	0.998	0.002
M70 Soft tissue disorders related to use, overuse and pressure	0.000	0.998	0.002
Y85.0 Sequelae of motor-vehicle accident	0.002	0.998	0.000
S32.30 Fracture of ilium (closed)	0.001	0.998	0.000
C67.9 Bladder, unspecified	0.000	0.998	0.002
R34 Anuria and oliguria	0.002	0.998	0.000
D56.9 Thalassaemia, unspecified	0.001	0.998	0.000
D56.8 Other thalassaemias	0.001	0.998	0.000
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]	0.001	0.998	0.000
D56.2 Delta-beta thalassaemia	0.001	0.998	0.000
D56.0 Alpha thalassaemia	0.001	0.998	0.000
F22.0 Delusional disorder	0.001	0.998	0.000
M70.2 Olecranon bursitis	0.000	0.998	0.001
F45.1 Undifferentiated somatoform disorder	0.000	0.999	0.001
F45.3 Somatoform autonomic dysfunction	0.000	0.999	0.001
G25.9 Extrapyramidal and movement disorder, unspecified	0.001	0.999	0.000
D50-D53 Nutritional anaemias	0.001	0.999	0.000
M70.22 Olecranon bursitis-Upper arm	0.000	0.999	0.001
F45.2 Hypochondriacal disorder	0.000	0.999	0.001
K82.1 Hydrops of gallbladder	0.001	0.999	0.000
Z30.5 Surveillance of (intra-uterine) contraceptive device	0.000	0.999	0.001
D25.9 Leiomyoma of uterus, unspecified	0.000	0.999	0.001
N95.1 Menopausal and female climacteric states	0.000	0.999	0.001
X62.0 Home	0.001	0.999	0.000
X62.7 Farm	0.001	0.999	0.000
X62.6 Industrial and construction area	0.001	0.999	0.000
X62.5 Trade and service area	0.001	0.999	0.000
X62.4 Street and highway	0.001	0.999	0.000
X62.3 Sports and athletics area	0.001	0.999	0.000
X62.2 School, other institution and public administrative area	0.001	0.999	0.000
X62.1 Residential institution	0.001	0.999	0.000
Z94.0 Kidney transplant status	0.000	0.999	0.001
M81.97 Osteoporosis, unspecified (Ankle and foot)	0.000	0.999	0.001
E06.1 Subacute thyroiditis	0.001	0.999	0.000
H34.8 Other retinal vascular occlusions	0.000	0.999	0.001
O99.0 Anaemia complicating pregnancy, childbirth and the puerperium	0.001	0.999	0.000
G12 Spinal muscular atrophy and related syndromes	0.000	0.999	0.001
M70.59 Other bursitis of knee-Site unspec	0.000	0.999	0.001
M70.58 Other bursitis of knee-Other	0.000	0.999	0.001
M70.57 Other bursitis of knee-Ankle/Foot	0.000	0.999	0.001
M70.55 Other bursitis of knee-Pelvic/Thigh	0.000	0.999	0.001
M70.54 Other bursitis of knee-Hand	0.000	0.999	0.001
M70.53 Other bursitis of knee-Forearm	0.000	0.999	0.001
M70.52 Other bursitis of knee-Upper arm	0.000	0.999	0.001
M70.51 Other bursitis of knee-Shldr region	0.000	0.999	0.001
M70.50 Other bursitis of knee-Mult sites	0.000	0.999	0.001
D56.1 Beta thalassaemia	0.001	0.999	0.000
G40.3 Generalised idiopathic epilepsy and epileptic syndromes	0.001	0.999	0.000
Q25.6 Stenosis of pulmonary artery	0.001	0.999	0.000
Q24 Other congenital malformations of heart	0.001	0.999	0.000
E06.5 Other chronic thyroiditis	0.001	0.999	0.000
M70.9 Unspecified soft tissue disorder related to use, overuse and pressure	0.000	0.999	0.001
M70.8 Other soft tissue disorders related to use, overuse and pressure	0.000	0.999	0.001
M70.1 Bursitis of hand	0.000	0.999	0.001
M70.0 Chronic crepitant synovitis of hand and wrist	0.000	0.999	0.001
V89.3 Person injured in unspecified nonmotor-vehicle accident, traffic	0.000	0.999	0.001
V89.1 Person injured in unspecified nonmotor-vehicle accident, nontraffic	0.000	0.999	0.001
V89.0 Person injured in unspecified motor-vehicle accident, nontraffic	0.000	0.999	0.001
M18.1 Other primary arthrosis of first carpometacarpal joint	0.001	0.999	0.000
V09.0 Pedestrian injured in nontraffic accident involving other and unspecified motor vehicles	0.001	0.999	0.000
X41.9 Unspecified place	0.001	0.999	0.000
X50.4 Street and highway	0.001	0.999	0.000
C34 Malignant neoplasm of bronchus and lung	0.000	0.999	0.001
K82.4 Cholesterolosis of gallbladder	0.001	0.999	0.000
Q61.3 Polycystic kidney, unspecified	0.000	0.999	0.001
D53 Other nutritional anaemias	0.001	0.999	0.000
D52 Folate deficiency anaemia	0.001	0.999	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.001	0.999	0.000
M70.29 Olecranon bursitis-Site unspec	0.000	0.999	0.001
M70.28 Olecranon bursitis-Other	0.000	0.999	0.001
M70.27 Olecranon bursitis-Ankle/Foot	0.000	0.999	0.001
M70.26 Olecranon bursitis-Lower Leg	0.000	0.999	0.001
M70.25 Olecranon bursitis-Pelvic/Thigh	0.000	0.999	0.001
M70.24 Olecranon bursitis-Hand	0.000	0.999	0.001
M70.23 Olecranon bursitis-Forearm	0.000	0.999	0.001
M70.21 Olecranon bursitis-Shldr region	0.000	0.999	0.001
M70.20 Olecranon bursitis-Mult sites	0.000	0.999	0.001
G72.0 Drug-induced myopathy	0.000	0.999	0.001
W22.9 Unspecified place	0.001	0.999	0.000
I15.1 Hypertension secondary to other renal disorders	0.000	0.999	0.001
K31.9 Disease of stomach and duodenum, unspecified	0.000	0.999	0.001
B91 Sequelae of poliomyelitis	0.000	0.999	0.001
K45 Other abdominal hernia	0.001	0.999	0.000
Q25 Congenital malformations of great arteries	0.001	0.999	0.000
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.001	0.999	0.000
D56.3 Thalassaemia trait	0.001	0.999	0.000
L94.0 Localised scleroderma [morphea]	0.001	0.999	0.000
M70.7 Other bursitis of hip	0.000	0.999	0.001
O99.5 Diseases of the respiratory system complicating pregnancy, childbirth and the puerperium	0.001	0.999	0.000
Q24.8 Other specified congenital malformations of heart	0.001	0.999	0.000
Q27.1 Congenital renal artery stenosis	0.001	0.999	0.000
S99.8 Other specified injuries of ankle and foot	0.000	0.999	0.001
X62.8 Other specified place	0.001	0.999	0.000
M19.17 Post-traumatic arthrosis of other joints (Ankle and foot)	0.000	0.999	0.001
X62.09 Intentional self-poisoning by and exposure to narcotics and psychodysleptics [hallucinogens], not elsewhere classified: Home: During unspecified activity	0.001	0.999	0.000
G12.9 Spinal muscular atrophy, unspecified	0.000	0.999	0.001
G12.8 Other spinal muscular atrophies and related syndromes	0.000	0.999	0.001
G12.1 Other inherited spinal muscular atrophy	0.000	0.999	0.001
G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]	0.000	0.999	0.001
G25 Other extrapyramidal and movement disorders	0.001	0.999	0.000
S06.80 Other intracranial injuries (without open intracranial wound)	0.000	0.999	0.001
F45.9 Somatoform disorder, unspecified	0.000	0.999	0.001
G72.4 Inflammatory myopathy, not elsewhere classified	0.000	0.999	0.001
Q24.4 Congenital subaortic stenosis	0.001	0.999	0.000
Q24.3 Pulmonary infundibular stenosis	0.001	0.999	0.000
Q24.2 Cor triatriatum	0.001	0.999	0.000
Q24.1 Levocardia	0.001	0.999	0.000
G72 Other myopathies	0.000	0.999	0.001
M41.99 Scoliosis, unspecified (Site unspecified)	0.001	0.999	0.000
M70.09 Chronic crepitant synovitis of hand and wrist-Site unspec	0.000	0.999	0.001
M70.08 Chronic crepitant synovitis of hand and wrist-Other	0.000	0.999	0.001
M70.07 Chronic crepitant synovitis of hand and wrist-Ankle/Foot	0.000	0.999	0.001
M70.06 Chronic crepitant synovitis of hand and wrist-Lower Leg	0.000	0.999	0.001
M70.05 Chronic crepitant synovitis of hand and wrist-Pelvic/Thigh	0.000	0.999	0.001
M70.04 Chronic crepitant synovitis of hand and wrist (Hand)	0.000	0.999	0.001
M70.03 Chronic crepitant synovitis of hand and wrist (Forearm)	0.000	0.999	0.001
M70.02 Chronic crepitant synovitis of hand and wrist-Upper arm	0.000	0.999	0.001
M70.01 Chronic crepitant synovitis of hand and wrist-Shldr region	0.000	0.999	0.001
M70.00 Chronic crepitant synovitis of hand and wrist (Multiple sites)	0.000	0.999	0.001
M70.19 Bursitis of hand-Site unspec	0.000	0.999	0.001
M70.18 Bursitis of hand-Other	0.000	0.999	0.001
M70.17 Bursitis of hand-Ankle/Foot	0.000	0.999	0.001
M70.16 Bursitis of hand-Lower Leg	0.000	0.999	0.001
M70.15 Bursitis of hand-Pelvic/Thigh	0.000	0.999	0.001
M70.14 Bursitis of hand-Hand	0.000	0.999	0.001
M70.13 Bursitis of hand-Forearm	0.000	0.999	0.001
M70.12 Bursitis of hand-Upper arm	0.000	0.999	0.001
M70.11 Bursitis of hand-Shldr region	0.000	0.999	0.001
M70.10 Bursitis of hand-Mult sites	0.000	0.999	0.001
M70.89 Other soft tissue disorders related to use, overuse and pressure (Site unspecified)	0.000	0.999	0.001
M70.88 Other soft tissue disorders related to use, overuse and pressure (Other)	0.000	0.999	0.001
M70.87 Other soft tissue disorders related to use, overuse and pressure (Ankle and foot)	0.000	0.999	0.001
M70.86 Other soft tissue disorders related to use, overuse and pressure (Lower leg)	0.000	0.999	0.001
M70.85 Other soft tissue disorders related to use, overuse and pressure (Pelvic region and thigh)	0.000	0.999	0.001
M70.84 Other soft tissue disorders related to use, overuse and pressure (Hand)	0.000	0.999	0.001
M70.83 Other soft tissue disorders related to use, overuse and pressure (Forearm)	0.000	0.999	0.001
M70.82 Other soft tissue disorders related to use, overuse and pressure (Upper arm)	0.000	0.999	0.001
M70.81 Other soft tissue disorders related to use, overuse and pressure (Shoulder region)	0.000	0.999	0.001
M70.80 Other soft tissue disorders related to use, overuse and pressure (Multiple sites)	0.000	0.999	0.001
M70.99 Unspecified soft tissue disorder related to use, overuse and pressure (Site unspecified)	0.000	0.999	0.001
M70.98 Unspecified soft tissue disorder related to use, overuse and pressure (Other)	0.000	0.999	0.001
M70.97 Unspecified soft tissue disorder related to use, overuse and pressure (Ankle and foot)	0.000	0.999	0.001
M70.96 Unspecified soft tissue disorder related to use, overuse and pressure (Lower leg)	0.000	0.999	0.001
M70.95 Unspecified soft tissue disorder related to use, overuse and pressure (Pelvic region and thigh)	0.000	0.999	0.001
M70.94 Unspecified soft tissue disorder related to use, overuse and pressure (Hand)	0.000	0.999	0.001
M70.93 Unspecified soft tissue disorder related to use, overuse and pressure (Forearm)	0.000	0.999	0.001
M70.92 Unspecified soft tissue disorder related to use, overuse and pressure (Upper arm)	0.000	0.999	0.001
M70.91 Unspecified soft tissue disorder related to use, overuse and pressure (Shoulder region)	0.000	0.999	0.001
M70.90 Unspecified soft tissue disorder related to use, overuse and pressure (Multiple sites)	0.000	0.999	0.001
C15.4 Middle third of oesophagus	0.001	0.999	0.000
D44.4 Craniopharyngeal duct	0.001	0.999	0.000
M43.0 Spondylolysis	0.000	0.999	0.001
M70.3 Other bursitis of elbow	0.000	0.999	0.001
S42.90 Fracture of shoulder girdle, part unspecified (closed)	0.000	0.999	0.001
A49.8 Other bacterial infections of unspecified site	0.000	0.999	0.001
A49.0 Staphylococcal infection, unspecified	0.000	0.999	0.001
C15.0 Cervical part of oesophagus	0.001	0.999	0.000
D52.8 Other folate deficiency anaemias	0.001	0.999	0.000
D52.1 Drug-induced folate deficiency anaemia	0.001	0.999	0.000
D52.0 Dietary folate deficiency anaemia	0.001	0.999	0.000
D53.8 Other specified nutritional anaemias	0.001	0.999	0.000
D53.2 Scorbutic anaemia	0.001	0.999	0.000
D53.0 Protein deficiency anaemia	0.001	0.999	0.000
I87.1 Compression of vein	0.001	0.999	0.000
Q25.4 Other congenital malformations of aorta	0.001	0.999	0.000
Q27 Other congenital malformations of peripheral vascular system	0.001	0.999	0.000
Q26 Congenital malformations of great veins	0.001	0.999	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.001	0.999	0.000
C15.1 Thoracic part of oesophagus	0.001	0.999	0.000
D52.9 Folate deficiency anaemia, unspecified	0.001	0.999	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.001	0.999	0.000
F80.1 Expressive language disorder	0.000	0.999	0.001
G72.8 Other specified myopathies	0.000	0.999	0.001
K45.1 Other specified abdominal hernia with gangrene	0.001	0.999	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.001	0.999	0.000
Q25.8 Other congenital malformations of great arteries	0.001	0.999	0.000
Q25.5 Atresia of pulmonary artery	0.001	0.999	0.000
Q25.3 Stenosis of aorta	0.001	0.999	0.000
Q25.2 Atresia of aorta	0.001	0.999	0.000
T83.6 Infection and inflammatory reaction due to prosthetic device, implant and graft in genital tract	0.001	0.999	0.000
M00.97 Pyogenic arthritis, unspecified (Ankle and foot)	0.001	0.999	0.000
M70.79 Other bursitis of hip-Site unspec	0.000	0.999	0.001
M70.78 Other bursitis of hip-Other	0.000	0.999	0.001
M70.77 Other bursitis of hip-Ankle/Foot	0.000	0.999	0.001
M70.76 Other bursitis of hip-Lower Leg	0.000	0.999	0.001
M70.74 Other bursitis of hip-Hand	0.000	0.999	0.001
M70.73 Other bursitis of hip-Forearm	0.000	0.999	0.001
M70.72 Other bursitis of hip-Upper arm	0.000	0.999	0.001
M70.71 Other bursitis of hip-Shldr region	0.000	0.999	0.001
M70.70 Other bursitis of hip-Mult sites	0.000	0.999	0.001
M81.95 Osteoporosis, unspecified (Pelvic region and thigh)	0.000	0.999	0.001
C34.0 Main bronchus	0.000	0.999	0.001
E53.9 Vitamin B deficiency, unspecified	0.001	0.999	0.000
M18.0 Primary arthrosis of first carpometacarpal joints, bilateral	0.001	0.999	0.000
Q24.6 Congenital heart block	0.001	0.999	0.000
Q24.0 Dextrocardia	0.001	0.999	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.001	0.999	0.000
Z29.1 Prophylactic immunotherapy	0.001	0.999	0.000
Q28 Other congenital malformations of circulatory system	0.001	0.999	0.000
S72.10 Pertrochanteric fracture (closed)	0.001	0.999	0.000
D53.9 Nutritional anaemia, unspecified	0.001	0.999	0.000
G25.6 Drug-induced tics and other tics of organic origin	0.001	0.999	0.000
G25.4 Drug-induced chorea	0.001	0.999	0.000
G72.3 Periodic paralysis	0.000	0.999	0.001
G72.2 Myopathy due to other toxic agents	0.000	0.999	0.001
G72.1 Alcoholic myopathy	0.000	0.999	0.001
C34.8 Overlapping lesion of bronchus and lung	0.000	0.999	0.001
C34.2 Middle lobe, bronchus or lung	0.000	0.999	0.001
G44.8 Other specified headache syndromes	0.001	0.999	0.000
H10.5 Blepharoconjunctivitis	0.001	0.999	0.000
H10.1 Acute atopic conjunctivitis	0.001	0.999	0.000
Q27.3 Peripheral arteriovenous malformation	0.001	0.999	0.000
C15 Malignant neoplasm of oesophagus	0.001	0.999	0.000
M43.08 Spondylolysis (Sacral and sacrococcygeal region)	0.000	0.999	0.001
M43.05 Spondylolysis (Thoracolumbar region)	0.000	0.999	0.001
M43.04 Spondylolysis (Thoracic region)	0.000	0.999	0.001
M43.03 Spondylolysis (Cervicothoracic region)	0.000	0.999	0.001
M43.01 Spondylolysis (Occipito-atlanto-axial region)	0.000	0.999	0.001
M43.00 Spondylolysis (Multiple sites in spine)	0.000	0.999	0.001
M70.39 Other bursitis of elbow-Site unspec	0.000	0.999	0.001
M70.38 Other bursitis of elbow-Other	0.000	0.999	0.001
M70.37 Other bursitis of elbow-Ankle/Foot	0.000	0.999	0.001
M70.36 Other bursitis of elbow-Lower Leg	0.000	0.999	0.001
M70.35 Other bursitis of elbow-Pelvic/Thigh	0.000	0.999	0.001
M70.34 Other bursitis of elbow-Hand	0.000	0.999	0.001
M70.33 Other bursitis of elbow-Forearm	0.000	0.999	0.001
M70.31 Other bursitis of elbow-Shldr region	0.000	0.999	0.001
M70.30 Other bursitis of elbow-Mult sites	0.000	0.999	0.001
C32.1 Supraglottis	0.000	0.999	0.001
Q07.0 Arnold-Chiari syndrome	0.001	0.999	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.001	0.999	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.001	0.999	0.000
Q20.6 Isomerism of atrial appendages	0.001	0.999	0.000
Q20.5 Discordant atrioventricular connexion	0.001	0.999	0.000
Q20.4 Double inlet ventricle	0.001	0.999	0.000
Q20.3 Discordant ventriculoarterial connexion	0.001	0.999	0.000
Q20.2 Double outlet left ventricle	0.001	0.999	0.000
Q20.1 Double outlet right ventricle	0.001	0.999	0.000
Q20.0 Common arterial trunk	0.001	0.999	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.001	0.999	0.000
Q25.0 Patent ductus arteriosus	0.001	0.999	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.001	0.999	0.000
Q26.8 Other congenital malformations of great veins	0.001	0.999	0.000
Q26.6 Portal vein-hepatic artery fistula	0.001	0.999	0.000
Q26.5 Anomalous portal venous connexion	0.001	0.999	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.001	0.999	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.001	0.999	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.001	0.999	0.000
Q26.1 Persistent left superior vena cava	0.001	0.999	0.000
Q26.0 Congenital stenosis of vena cava	0.001	0.999	0.000
Q27.4 Congenital phlebectasia	0.001	0.999	0.000
Q27.2 Other congenital malformations of renal artery	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