TreeWAS – Variant ID: rs73320584

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
D22.3 Melanocytic naevi of other and unspecified parts of face	0.000	0.940	0.060
D50.8 Other iron deficiency anaemias	0.040	0.960	0.000
D23.3 Skin of other and unspecified parts of face	0.033	0.967	0.000
L72.9 Follicular cyst of skin and subcutaneous tissue, unspecified	0.017	0.983	0.000
H00.1 Chalazion	0.012	0.988	0.000
J38.7 Other diseases of larynx	0.000	0.990	0.010
C44.2 Skin of ear and external auricular canal	0.010	0.990	0.000
D50 Iron deficiency anaemia	0.010	0.990	0.000
J38.3 Other diseases of vocal cords	0.000	0.991	0.009
M18.1 Other primary arthrosis of first carpometacarpal joint	0.000	0.992	0.008
J38 Diseases of vocal cords and larynx, not elsewhere classified	0.000	0.992	0.008
L81.4 Other melanin hyperpigmentation	0.008	0.992	0.000
D23 Other benign neoplasms of skin	0.008	0.992	0.000
J38.4 Oedema of larynx	0.000	0.993	0.007
D23.2 Skin of ear and external auricular canal	0.007	0.993	0.000
D50.1 Sideropenic dysphagia	0.007	0.993	0.000
J38.0 Paralysis of vocal cords and larynx	0.000	0.993	0.007
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)	0.007	0.993	0.000
J38.5 Laryngeal spasm	0.000	0.994	0.006
D18.0 Haemangioma, any site	0.000	0.994	0.006
J38.6 Stenosis of larynx	0.000	0.994	0.006
D23.6 Skin of upper limb, including shoulder	0.006	0.994	0.000
D23.4 Skin of scalp and neck	0.006	0.994	0.000
J06.9 Acute upper respiratory infection, unspecified	0.005	0.995	0.000
H00 Hordeolum and chalazion	0.005	0.995	0.000
S49.9 Unspecified injury of shoulder and upper arm	0.000	0.995	0.005
Z39.1 Care and examination of lactating mother	0.000	0.995	0.005
D23.0 Skin of lip	0.005	0.995	0.000
H35.8 Other specified retinal disorders	0.005	0.995	0.000
L81 Other disorders of pigmentation	0.005	0.995	0.000
J38.1 Polyp of vocal cord and larynx	0.000	0.995	0.005
D23.9 Skin, unspecified	0.005	0.995	0.000
C20 Malignant neoplasm of rectum	0.005	0.995	0.000
M25.64 Stiffness of joint, not elsewhere classified (Hand)	0.005	0.995	0.000
E80.4 Gilbert's syndrome	0.000	0.995	0.005
D50-D53 Nutritional anaemias	0.005	0.995	0.000
H35.3 Degeneration of macula and posterior pole	0.005	0.995	0.000
J38.2 Nodules of vocal cords	0.000	0.995	0.004
M25.6 Stiffness of joint, not elsewhere classified	0.004	0.996	0.000
L81.8 Other specified disorders of pigmentation	0.004	0.996	0.000
M18 Arthrosis of first carpometacarpal joint	0.000	0.996	0.004
D23.1 Skin of eyelid, including canthus	0.004	0.996	0.000
O02.1 Missed abortion	0.000	0.996	0.004
K86.2 Cyst of pancreas	0.004	0.996	0.000
H35 Other retinal disorders	0.004	0.996	0.000
M25.61 Stiffness of joint, not elsewhere classified (Shoulder region)	0.004	0.996	0.000
M18.9 Arthrosis of first carpometacarpal joint, unspecified	0.000	0.996	0.004
H35.0 Background retinopathy and retinal vascular changes	0.004	0.996	0.000
L81.9 Disorder of pigmentation, unspecified	0.004	0.996	0.000
M25.63 Stiffness of joint, not elsewhere classified (Forearm)	0.004	0.996	0.000
H00.0 Hordeolum and other deep inflammation of eyelid	0.004	0.996	0.000
M25.67 Stiffness of joint, not elsewhere classified (Ankle and foot)	0.004	0.996	0.000
L81.7 Pigmented purpuric dermatosis	0.004	0.996	0.000
L81.6 Other disorders of diminished melanin formation	0.004	0.996	0.000
L81.5 Leukoderma, not elsewhere classified	0.004	0.996	0.000
L81.3 Cafe au lait spots	0.004	0.996	0.000
L81.1 Chloasma	0.004	0.996	0.000
L81.0 Postinflammatory hyperpigmentation	0.004	0.996	0.000
M25.66 Stiffness of joint, not elsewhere classified (Lower leg)	0.004	0.996	0.000
L81.2 Freckles	0.003	0.996	0.000
M25.68 Stiffness of joint, not elsewhere classified (Other)	0.003	0.996	0.000
D23.5 Skin of trunk	0.004	0.996	0.000
D23.7 Skin of lower limb, including hip	0.003	0.996	0.000
D53 Other nutritional anaemias	0.003	0.996	0.000
S42.00 Fracture of clavicle (closed)	0.000	0.996	0.003
M25.62 Stiffness of joint, not elsewhere classified (Upper arm)	0.003	0.997	0.000
D52 Folate deficiency anaemia	0.003	0.997	0.000
H35.2 Other proliferative retinopathy	0.003	0.997	0.000
K63.3 Ulcer of intestine	0.000	0.997	0.003
M25.69 Stiffness of joint, not elsewhere classified (Site unspecified)	0.003	0.997	0.000
M25.65 Stiffness of joint, not elsewhere classified (Pelvic region and thigh)	0.003	0.997	0.000
M25.60 Stiffness of joint, not elsewhere classified (Multiple sites)	0.003	0.997	0.000
H35.6 Retinal haemorrhage	0.003	0.997	0.000
M18.5 Other secondary arthrosis of first carpometacarpal joint	0.000	0.997	0.003
M18.4 Other secondary arthrosis of first carpometacarpal joints, bilateral	0.000	0.997	0.003
M18.3 Other posttraumatic arthrosis of first carpometacarpal joint	0.000	0.997	0.003
M18.2 Posttraumatic arthrosis of first carpometacarpal joints, bilateral	0.000	0.997	0.003
O02.0 Blighted ovum and nonhydatidiform mole	0.000	0.997	0.003
S49 Other and unspecified injuries of shoulder and upper arm	0.000	0.997	0.003
H35.1 Retinopathy of prematurity	0.003	0.997	0.000
O02 Other abnormal products of conception	0.000	0.997	0.003
H35.7 Separation of retinal layers	0.003	0.997	0.000
T81.3 Disruption of operation wound, not elsewhere classified	0.003	0.997	0.000
H35.9 Retinal disorder, unspecified	0.003	0.997	0.000
M18.0 Primary arthrosis of first carpometacarpal joints, bilateral	0.000	0.997	0.003
D53.8 Other specified nutritional anaemias	0.003	0.997	0.000
D53.2 Scorbutic anaemia	0.003	0.997	0.000
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.003	0.997	0.000
D53.0 Protein deficiency anaemia	0.003	0.997	0.000
Y42.5 Other oestrogens and progestogens	0.003	0.997	0.000
D51 Vitamin B12 deficiency anaemia	0.003	0.997	0.000
D52.8 Other folate deficiency anaemias	0.003	0.997	0.000
D52.1 Drug-induced folate deficiency anaemia	0.003	0.997	0.000
D52.0 Dietary folate deficiency anaemia	0.003	0.997	0.000
D53.9 Nutritional anaemia, unspecified	0.003	0.997	0.000
M35.3 Polymyalgia rheumatica	0.003	0.997	0.000
H35.4 Peripheral retinal degeneration	0.003	0.997	0.000
S49.8 Other specified injuries of shoulder and upper arm	0.000	0.997	0.002
S49.7 Multiple injuries of shoulder and upper arm	0.000	0.997	0.002
D18 Haemangioma and lymphangioma, any site	0.000	0.997	0.003
D52.9 Folate deficiency anaemia, unspecified	0.002	0.997	0.000
O02.9 Abnormal product of conception, unspecified	0.000	0.997	0.002
O02.8 Other specified abnormal products of conception	0.000	0.997	0.002
M65.91 Synovitis and tenosynovitis, unspecified (Shoulder region)	0.003	0.997	0.000
S42.0 Fracture of clavicle	0.000	0.997	0.002
J06 Acute upper respiratory infections of multiple and unspecified sites	0.002	0.997	0.000
Y44.2 Anticoagulants	0.002	0.998	0.000
H65.4 Other chronic nonsuppurative otitis media	0.002	0.998	0.000
D80-D89 Certain disorders involving the immune mechanism	0.002	0.998	0.000
D69.3 Idiopathic thrombocytopenic purpura	0.002	0.998	0.000
S46.0 Injury of tendon of the rotator cuff of shoulder	0.000	0.998	0.002
D51.8 Other vitamin B12 deficiency anaemias	0.002	0.998	0.000
D51.3 Other dietary vitamin B12 deficiency anaemia	0.002	0.998	0.000
D51.2 Transcobalamin II deficiency	0.002	0.998	0.000
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria	0.002	0.998	0.000
D68.3 Haemorrhagic disorder due to circulating anticoagulants	0.002	0.998	0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.002	0.998	0.000
S46.2 Injury of muscle and tendon of other parts of biceps	0.000	0.998	0.002
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.002	0.998	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.002	0.998	0.000
H35.5 Hereditary retinal dystrophy	0.002	0.998	0.000
D80 Immunodeficiency with predominantly antibody defects	0.002	0.998	0.000
C21.1 Anal canal	0.002	0.998	0.000
O47.1 False labour at or after 37 completed weeks of gestation	0.000	0.998	0.002
S46 Injury of muscle and tendon at shoulder and upper arm level	0.000	0.998	0.002
K86.9 Disease of pancreas, unspecified	0.002	0.998	0.000
H34 Retinal vascular occlusions	0.002	0.998	0.000
H30-H36 Disorders of choroid and retina	0.002	0.998	0.000
T31.0 Burns involving less than 10% of body surface	0.000	0.998	0.002
S42.01 Fracture of clavicle (open)	0.000	0.998	0.002
D18.1 Lymphangioma, any site	0.000	0.998	0.002
E53.8 Deficiency of other specified B group vitamins	0.002	0.998	0.000
O47.9 False labour, unspecified	0.000	0.998	0.002
S32.00 Fracture of lumbar vertebra (closed)	0.002	0.998	0.000
J06.8 Other acute upper respiratory infections of multiple sites	0.002	0.998	0.000
J06.0 Acute laryngopharyngitis	0.002	0.998	0.000
Q76.0 Spina bifida occulta	0.000	0.998	0.002
R30.0 Dysuria	0.002	0.998	0.000
D84 Other immunodeficiencies	0.002	0.998	0.000
L93.0 Discoid lupus erythematosus	0.002	0.998	0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.002	0.998	0.000
H34.9 Retinal vascular occlusion, unspecified	0.002	0.998	0.000
E80 Disorders of porphyrin and bilirubin metabolism	0.000	0.998	0.002
C21.0 Anus, unspecified	0.002	0.998	0.000
D75.2 Essential thrombocytosis	0.002	0.998	0.000
M17.0 Primary gonarthrosis, bilateral	0.000	0.998	0.002
H34.2 Other retinal artery occlusions	0.002	0.998	0.000
D69 Purpura and other haemorrhagic conditions	0.002	0.998	0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions	0.002	0.998	0.000
D83 Common variable immunodeficiency	0.002	0.998	0.000
D82 Immunodeficiency associated with other major defects	0.002	0.998	0.000
D81 Combined immunodeficiencies	0.002	0.998	0.000
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency	0.002	0.998	0.000
D76.3 Other histiocytosis syndromes	0.002	0.998	0.000
C21 Malignant neoplasm of anus and anal canal	0.002	0.998	0.000
H30 Chorioretinal inflammation	0.002	0.998	0.000
C32.9 Larynx, unspecified	0.000	0.998	0.002
D80.1 Nonfamilial hypogammaglobulinaemia	0.002	0.998	0.000
Y51.7 Beta-Adrenoreceptor antagonists, not elsewhere classified	0.000	0.998	0.002
D69.4 Other primary thrombocytopenia	0.002	0.998	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.002	0.998	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.002	0.998	0.000
D89.3 Immune reconstitution syndrome	0.002	0.998	0.000
D89.1 Cryoglobulinaemia	0.002	0.998	0.000
D89.0 Polyclonal hypergammaglobulinaemia	0.002	0.998	0.000
O47 False labour	0.000	0.998	0.002
D84.9 Immunodeficiency, unspecified	0.002	0.998	0.000
Q76 Congenital malformations of spine and bony thorax	0.000	0.998	0.002
D55-D59 Haemolytic anaemias	0.002	0.998	0.000
S40-S49 Injuries to the shoulder and upper arm	0.000	0.998	0.002
C22.1 Intrahepatic bile duct carcinoma	0.002	0.998	0.000
N95.2 Postmenopausal atrophic vaginitis	0.002	0.998	0.000
H31 Other disorders of choroid	0.002	0.998	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.002	0.998	0.000
D80.8 Other immunodeficiencies with predominantly antibody defects	0.002	0.998	0.000
D80.7 Transient hypogammaglobulinaemia of infancy	0.002	0.998	0.000
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.002	0.998	0.000
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.002	0.998	0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.002	0.998	0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.002	0.998	0.000
D80.0 Hereditary hypogammaglobulinaemia	0.002	0.998	0.000
D86 Sarcoidosis	0.002	0.998	0.000
C22.9 Liver, unspecified	0.002	0.998	0.000
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.000	0.998	0.002
S46.8 Injury of other muscles and tendons at shoulder and upper arm level	0.000	0.998	0.002
S46.7 Injury of multiple muscles and tendons at shoulder and upper arm level	0.000	0.998	0.002
S46.3 Injury of muscle and tendon of triceps	0.000	0.998	0.002
H32 Chorioretinal disorders in diseases classified elsewhere	0.002	0.998	0.000
H30.9 Chorioretinal inflammation, unspecified	0.002	0.998	0.000
H34.0 Transient retinal artery occlusion	0.002	0.998	0.000
C21.8 Overlapping lesion of rectum, anus and anal canal	0.002	0.998	0.000
H34.1 Central retinal artery occlusion	0.002	0.998	0.000
C22 Malignant neoplasm of liver and intrahepatic bile ducts	0.002	0.998	0.000
O47.0 False labour before 37 completed weeks of gestation	0.000	0.998	0.002
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.002	0.998	0.000
C26.0 Intestinal tract, part 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
D86.9 Sarcoidosis, unspecified	0.002	0.998	0.000
H34.8 Other retinal vascular occlusions	0.002	0.998	0.000
S42 Fracture of shoulder and upper arm	0.000	0.998	0.002
D51.9 Vitamin B12 deficiency anaemia, unspecified	0.002	0.998	0.000
D86.1 Sarcoidosis of lymph nodes	0.002	0.998	0.000
C22.0 Liver cell carcinoma	0.002	0.998	0.000
O36.0 Maternal care for rhesus isoimmunisation	0.000	0.998	0.002
Q27.3 Peripheral arteriovenous malformation	0.000	0.998	0.002
M05.90 Seropositive rheumatoid arthritis, unspecified (Multiple sites)	0.002	0.998	0.000
S52.20 Fracture of shaft of ulna (closed)	0.002	0.998	0.000
E80.7 Disorder of bilirubin metabolism, unspecified	0.000	0.998	0.002
E80.6 Other disorders of bilirubin metabolism	0.000	0.998	0.002
E80.5 Crigler-Najjar syndrome	0.000	0.998	0.002
E80.3 Defects of catalase and peroxydase	0.000	0.998	0.002
E80.2 Other porphyria	0.000	0.998	0.002
E80.1 Porphyria cutanea tarda	0.000	0.998	0.002
E80.0 Hereditary erythropoietic porphyria	0.000	0.998	0.002
S46.1 Injury of muscle and tendon of long head of biceps	0.000	0.998	0.002
L72 Follicular cysts of skin and subcutaneous tissue	0.002	0.998	0.000
M70.65 Trochanteric bursitis-Pelvic/Thigh	0.002	0.998	0.000
D69.8 Other specified haemorrhagic conditions	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
D67 Hereditary factor IX deficiency	0.002	0.998	0.000
D65 Disseminated intravascular coagulation [defibrination syndrome]	0.002	0.998	0.000
D81.9 Combined immunodeficiency, unspecified	0.001	0.998	0.000
D81.8 Other combined immunodeficiencies	0.001	0.998	0.000
D81.7 Major histocompatibility complex class II deficiency	0.001	0.998	0.000
D81.6 Major histocompatibility complex class I deficiency	0.001	0.998	0.000
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.001	0.998	0.000
D81.4 Nezelof's syndrome	0.001	0.998	0.000
D81.3 Adenosine deaminase [ADA] deficiency	0.001	0.998	0.000
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.001	0.998	0.000
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.001	0.998	0.000
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.001	0.998	0.000
D82.9 Immunodeficiency associated with major defect, unspecified	0.001	0.998	0.000
D82.8 Immunodeficiency associated with other specified major defects	0.001	0.998	0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.001	0.998	0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.001	0.998	0.000
D82.2 Immunodeficiency with short-limbed stature	0.001	0.998	0.000
D82.1 Di George's syndrome	0.001	0.998	0.000
D82.0 Wiskott-Aldrich syndrome	0.001	0.998	0.000
D83.9 Common variable immunodeficiency, unspecified	0.001	0.998	0.000
D83.8 Other common variable immunodeficiencies	0.001	0.998	0.000
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells	0.001	0.998	0.000
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders	0.001	0.998	0.000
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function	0.001	0.998	0.000
H31.1 Choroidal degeneration	0.002	0.998	0.000
H33.0 Retinal detachment with retinal break	0.002	0.998	0.000
N81.4 Uterovaginal prolapse, unspecified	0.002	0.998	0.000
T42.6 Other antiepileptic and sedative-hypnotic drugs	0.000	0.998	0.002
D58 Other hereditary haemolytic anaemias	0.002	0.998	0.000
C21.2 Cloacogenic zone	0.002	0.998	0.000
C44.4 Skin of scalp and neck	0.002	0.998	0.000
H30.8 Other chorioretinal inflammations	0.001	0.998	0.000
H30.2 Posterior cyclitis	0.001	0.998	0.000
H30.1 Disseminated chorioretinal inflammation	0.001	0.998	0.000
H30.0 Focal chorioretinal inflammation	0.001	0.998	0.000
K86 Other diseases of pancreas	0.002	0.998	0.000
Y44 Agents primarily affecting blood constituents	0.002	0.998	0.000
D70-D77 Other diseases of blood and blood-forming organs	0.002	0.998	0.000
C32.0 Glottis	0.000	0.998	0.002
D69.9 Haemorrhagic condition, unspecified	0.002	0.998	0.000
D69.5 Secondary thrombocytopenia	0.002	0.998	0.000
Q12.0 Congenital cataract	0.000	0.998	0.002
S46.9 Injury of unspecified muscle and tendon at shoulder and upper arm level	0.000	0.998	0.001
D57 Sickle-cell disorders	0.001	0.998	0.000
D56 Thalassaemia	0.001	0.998	0.000
D55 Anaemia due to enzyme disorders	0.001	0.998	0.000
D75 Other diseases of blood and blood-forming organs	0.002	0.998	0.000
M25.36 Other instability of joint (Lower leg)	0.002	0.998	0.000
C45.9 Mesothelioma, unspecified	0.000	0.998	0.002
D69.0 Allergic purpura	0.001	0.998	0.000
H31.0 Chorioretinal scars	0.001	0.998	0.000
K11.9 Disease of salivary gland, unspecified	0.002	0.998	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.000	0.998	0.001
Q76.8 Other congenital malformations of bony thorax	0.000	0.998	0.001
Q76.7 Congenital malformation of sternum	0.000	0.998	0.001
Q76.6 Other congenital malformations of ribs	0.000	0.998	0.001
Q76.5 Cervical rib	0.000	0.998	0.001
Q76.3 Congenital scoliosis due to congenital bony malformation	0.000	0.998	0.001
Q76.2 Congenital spondylolisthesis	0.000	0.998	0.001
Q76.1 Klippel-Feil syndrome	0.000	0.998	0.001
C32 Malignant neoplasm of larynx	0.000	0.998	0.002
S48 Traumatic amputation of shoulder and upper arm	0.000	0.998	0.001
S45 Injury of blood vessels at shoulder and upper arm level	0.000	0.998	0.001
S44 Injury of nerves at shoulder and upper arm level	0.000	0.998	0.001
S47 Crushing injury of shoulder and upper arm	0.000	0.998	0.001
M65.97 Synovitis and tenosynovitis, unspecified (Ankle and foot)	0.002	0.998	0.000
C45.0 Mesothelioma of pleura	0.000	0.998	0.002
D73.5 Infarction of spleen	0.002	0.998	0.000
H31.9 Disorder of choroid, unspecified	0.001	0.998	0.000
H31.4 Choroidal detachment	0.001	0.998	0.000
H31.3 Choroidal haemorrhage and rupture	0.001	0.998	0.000
H31.2 Hereditary choroidal dystrophy	0.001	0.998	0.000
H53.2 Diplopia	0.002	0.998	0.000
H33 Retinal detachments and breaks	0.002	0.998	0.000
D58.0 Hereditary spherocytosis	0.001	0.998	0.000
D86.3 Sarcoidosis of skin	0.001	0.998	0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.001	0.998	0.000
H32.8 Other chorioretinal disorders in diseases classified elsewhere	0.001	0.998	0.000
H32.0 Chorioretinal inflammation in infectious and parasitic diseases classified elsewhere	0.001	0.998	0.000
D66 Hereditary factor VIII deficiency	0.001	0.998	0.000
C17.9 Small intestine, unspecified	0.002	0.998	0.000
C22.7 Other specified carcinomas of liver	0.001	0.998	0.000
C22.4 Other sarcomas of liver	0.001	0.998	0.000
C22.3 Angiosarcoma of liver	0.001	0.998	0.000
C22.2 Hepatoblastoma	0.001	0.998	0.000
D68.6 Other Thrombophilia	0.001	0.998	0.000
D76.2 Haemophagocytic syndrome, infection-associated	0.001	0.998	0.000
D76.1 Haemophagocytic lymphohistiocytosis	0.001	0.998	0.000
D76.0 Langerhans' cell histiocytosis, not elsewhere classified	0.001	0.998	0.000
M22.3 Other derangements of patella	0.002	0.998	0.000
O36.6 Maternal care for excessive foetal growth	0.000	0.998	0.002
K63.8 Other specified diseases of intestine	0.000	0.998	0.002
S42.8 Fracture of other parts of shoulder and upper arm	0.000	0.998	0.001
D59 Acquired haemolytic anaemia	0.001	0.998	0.000
S43 Dislocation, sprain and strain of joints and ligaments of shoulder girdle	0.000	0.998	0.001
H31.8 Other specified disorders of choroid	0.001	0.998	0.000
S42.7 Multiple fractures of clavicle, scapula and humerus	0.000	0.998	0.001
D73 Diseases of spleen	0.002	0.998	0.000
S41 Open wound of shoulder and upper arm	0.000	0.998	0.001
G83.4 Cauda equina syndrome	0.001	0.998	0.000
H33.4 Traction detachment of retina	0.001	0.998	0.000
L72.2 Steatocystoma multiplex	0.001	0.998	0.000
C17.2 Ileum	0.001	0.998	0.000
Y40.8 Other systemic antibiotics	0.001	0.998	0.000
D68 Other coagulation defects	0.001	0.998	0.000
D58.8 Other specified hereditary haemolytic anaemias	0.001	0.999	0.000
D58.2 Other haemoglobinopathies	0.001	0.999	0.000
D58.1 Hereditary elliptocytosis	0.001	0.999	0.000
G99.2 Myelopathy in diseases classified elsewhere	0.000	0.999	0.001
G20 Parkinson's disease	0.000	0.999	0.001
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.000	0.999	0.001
D86.8 Sarcoidosis of other and combined sites	0.001	0.999	0.000
L72.8 Other follicular cysts of skin and subcutaneous tissue	0.001	0.999	0.000
O71.4 Obstetric high vaginal laceration alone	0.001	0.999	0.000
Y44.9 Other and unspecified agents affecting blood constituents	0.001	0.999	0.000
Y44.7 Plasma substitutes	0.001	0.999	0.000
Y44.6 Natural blood and blood products	0.001	0.999	0.000
Y44.5 Thrombolytic drugs	0.001	0.999	0.000
Y44.4 Antithrombotic drugs [platelet-aggregation inhibitors]	0.001	0.999	0.000
Y44.3 Anticoagulant antagonists, vitamin K and other coagulants	0.001	0.999	0.000
Y44.1 Vitamin B12, folic acid and other anti-megaloblastic-anaemia preparations	0.001	0.999	0.000
Y44.0 Iron preparations and other anti-hypochromic-anaemia preparations	0.001	0.999	0.000
C26 Malignant neoplasm of other and ill-defined digestive organs	0.001	0.999	0.000
D74 Methaemoglobinaemia	0.001	0.999	0.000
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere	0.001	0.999	0.000
D71 Functional disorders of polymorphonuclear neutrophils	0.001	0.999	0.000
M05.97 Seropositive rheumatoid arthritis, unspecified (Ankle and foot)	0.001	0.999	0.000
D55.9 Anaemia due to enzyme disorder, unspecified	0.001	0.999	0.000
D55.8 Other anaemias due to enzyme disorders	0.001	0.999	0.000
D55.3 Anaemia due to disorders of nucleotide metabolism	0.001	0.999	0.000
D55.2 Anaemia due to disorders of glycolytic enzymes	0.001	0.999	0.000
D55.1 Anaemia due to other disorders of glutathione metabolism	0.001	0.999	0.000
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency	0.001	0.999	0.000
D56.9 Thalassaemia, unspecified	0.001	0.999	0.000
D56.8 Other thalassaemias	0.001	0.999	0.000
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]	0.001	0.999	0.000
D56.3 Thalassaemia trait	0.001	0.999	0.000
D56.2 Delta-beta thalassaemia	0.001	0.999	0.000
D56.1 Beta thalassaemia	0.001	0.999	0.000
D56.0 Alpha thalassaemia	0.001	0.999	0.000
D57.8 Other sickle-cell disorders	0.001	0.999	0.000
D57.3 Sickle-cell trait	0.001	0.999	0.000
D57.2 Double heterozygous sickling disorders	0.001	0.999	0.000
D57.1 Sickle-cell anaemia without crisis	0.001	0.999	0.000
D57.0 Sickle-cell anaemia with crisis	0.001	0.999	0.000
D75.8 Other specified diseases of blood and blood-forming organs	0.001	0.999	0.000
D75.0 Familial erythrocytosis	0.001	0.999	0.000
H33.5 Other retinal detachments	0.001	0.999	0.000
O36.9 Maternal care for foetal problem, unspecified	0.000	0.999	0.001
S42.4 Fracture of lower end of humerus	0.000	0.999	0.001
T82.0 Mechanical complication of heart valve prosthesis	0.000	0.999	0.001
Y55.6 Antiasthmatics, not elsewhere classified	0.001	0.999	0.000
Q65 Congenital deformities of hip	0.000	0.999	0.001
C32.8 Overlapping lesion of larynx	0.000	0.999	0.001
C32.3 Laryngeal cartilage	0.000	0.999	0.001
C32.2 Subglottis	0.000	0.999	0.001
Q65.8 Other congenital deformities of hip	0.000	0.999	0.001
S44.9 Injury of unspecified nerve at shoulder and upper arm level	0.000	0.999	0.001
S44.8 Injury of other nerves at shoulder and upper arm level	0.000	0.999	0.001
S44.7 Injury of multiple nerves at shoulder and upper arm level	0.000	0.999	0.001
S44.5 Injury of cutaneous sensory nerve at shoulder and upper arm level	0.000	0.999	0.001
S44.4 Injury of musculocutaneous nerve	0.000	0.999	0.001
S44.3 Injury of axillary nerve	0.000	0.999	0.001
S44.2 Injury of radial nerve at upper arm level	0.000	0.999	0.001
S44.1 Injury of median nerve at upper arm level	0.000	0.999	0.001
S44.0 Injury of ulnar nerve at upper arm level	0.000	0.999	0.001
S45.9 Injury of unspecified blood vessel at shoulder and upper arm level	0.000	0.999	0.001
S45.8 Injury of other blood vessels at shoulder and upper arm level	0.000	0.999	0.001
S45.7 Injury of multiple blood vessels at shoulder and upper arm level	0.000	0.999	0.001
S45.3 Injury of superficial vein at shoulder and upper arm level	0.000	0.999	0.001
S45.2 Injury of axillary or brachial vein	0.000	0.999	0.001
S45.1 Injury of brachial artery	0.000	0.999	0.001
S45.0 Injury of axillary artery	0.000	0.999	0.001
S48.9 Traumatic amputation of shoulder and upper arm, level unspecified	0.000	0.999	0.001
S48.1 Traumatic amputation at level between shoulder and elbow	0.000	0.999	0.001
S48.0 Traumatic amputation at shoulder joint	0.000	0.999	0.001
C32.1 Supraglottis	0.000	0.999	0.001
D58.9 Hereditary haemolytic anaemia, unspecified	0.001	0.999	0.000
E21.3 Hyperparathyroidism, unspecified	0.001	0.999	0.000
Y41.8 Other specified systemic anti-infectives and antiparasitics	0.001	0.999	0.000
Y41.5 Antiviral drugs	0.001	0.999	0.000
Z74.9 Problem related to care-provider dependency, unspecified	0.001	0.999	0.000
C17 Malignant neoplasm of small intestine	0.001	0.999	0.000
Q12 Congenital lens malformations	0.000	0.999	0.001
D73.1 Hypersplenism	0.001	0.999	0.000
H33.1 Retinoschisis and retinal cysts	0.001	0.999	0.000
O99.6 Diseases of the digestive system complicating pregnancy, childbirth and the puerperium	0.000	0.999	0.001
S42.2 Fracture of upper end of humerus	0.000	0.999	0.001
S42.81 Fracture of other parts of shoulder and upper arm (open)	0.000	0.999	0.001
S42.80 Fracture of other parts of shoulder and upper arm (closed)	0.000	0.999	0.001
C34.9 Bronchus or lung, unspecified	0.000	0.999	0.001
S43.7 Sprain and strain of other and unspecified parts of shoulder girdle	0.000	0.999	0.001
S43.6 Sprain and strain of sternoclavicular joint	0.000	0.999	0.001
S43.5 Sprain and strain of acromioclavicular joint	0.000	0.999	0.001
S43.3 Dislocation of other and unspecified parts of shoulder girdle	0.000	0.999	0.001
S43.2 Dislocation of sternoclavicular joint	0.000	0.999	0.001
S43.0 Dislocation of shoulder joint	0.000	0.999	0.001
M25.31 Other instability of joint (Shoulder region)	0.001	0.999	0.000
M65.86 Other synovitis and tenosynovitis (Lower leg)	0.001	0.999	0.000
S42.71 Multiple fractures of clavicle, scapula and humerus (open)	0.000	0.999	0.001
D59.9 Acquired haemolytic anaemia, unspecified	0.001	0.999	0.000
D59.8 Other acquired haemolytic anaemias	0.001	0.999	0.000
D59.6 Haemoglobinuria due to haemolysis from other external causes	0.001	0.999	0.000
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]	0.001	0.999	0.000
D59.4 Other nonautoimmune haemolytic anaemias	0.001	0.999	0.000
D59.3 Haemolytic-uraemic syndrome	0.001	0.999	0.000
D59.2 Drug-induced nonautoimmune haemolytic anaemia	0.001	0.999	0.000
D59.0 Drug-induced autoimmune haemolytic anaemia	0.001	0.999	0.000
D73.9 Disease of spleen, unspecified	0.001	0.999	0.000
D73.4 Cyst of spleen	0.001	0.999	0.000
D73.3 Abscess of spleen	0.001	0.999	0.000
D73.2 Chronic congestive splenomegaly	0.001	0.999	0.000
K86.3 Pseudocyst of pancreas	0.001	0.999	0.000
S30.1 Contusion of abdominal wall	0.001	0.999	0.000
S41.8 Open wound of other and unspecified parts of shoulder girdle	0.000	0.999	0.001
S41.7 Multiple open wounds of shoulder and upper arm	0.000	0.999	0.001
S41.0 Open wound of shoulder	0.000	0.999	0.001
S42.9 Fracture of shoulder girdle, part unspecified	0.000	0.999	0.001
S43.1 Dislocation of acromioclavicular joint	0.000	0.999	0.001
M65.84 Other synovitis and tenosynovitis (Hand)	0.001	0.999	0.000
D68.4 Acquired coagulation factor deficiency	0.001	0.999	0.000
D68.1 Hereditary factor XI deficiency	0.001	0.999	0.000
D73.8 Other diseases of spleen	0.001	0.999	0.000
M05.9 Seropositive rheumatoid arthritis, unspecified	0.001	0.999	0.000
S32.0 Fracture of lumbar vertebra	0.001	0.999	0.000
M70.46 Prepatellar bursitis-Lower Leg	0.000	0.999	0.001
M89.87 Other specified disorders of bone (Ankle and foot)	0.001	0.999	0.000
S42.70 Multiple fractures of clavicle, scapula and humerus (closed)	0.000	0.999	0.001
Q18.1 Preauricular sinus and cyst	0.000	0.999	0.001
Z71.8 Other specified counselling	0.001	0.999	0.000
Q78 Other osteochondrodysplasias	0.000	0.999	0.001
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.000	0.999	0.001
Q75 Other congenital malformations of skull and face bones	0.000	0.999	0.001
Q74 Other congenital malformations of limb(s)	0.000	0.999	0.001
Q73 Reduction defects of unspecified limb	0.000	0.999	0.001
Q72 Reduction defects of lower limb	0.000	0.999	0.001
Q71 Reduction defects of upper limb	0.000	0.999	0.001
Q70 Syndactyly	0.000	0.999	0.001
Q69 Polydactyly	0.000	0.999	0.001
Q68 Other congenital musculoskeletal deformities	0.000	0.999	0.001
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.000	0.999	0.001
M25.34 Other instability of joint (Hand)	0.001	0.999	0.000
C26.8 Overlapping lesion of digestive system	0.001	0.999	0.000
C26.1 Spleen	0.001	0.999	0.000
D74.9 Methaemoglobinaemia, unspecified	0.001	0.999	0.000
D74.8 Other methaemoglobinaemias	0.001	0.999	0.000
D74.0 Congenital methaemoglobinaemia	0.001	0.999	0.000
E55.9 Vitamin D deficiency, unspecified	0.000	0.999	0.001
M65.9 Synovitis and tenosynovitis, unspecified	0.001	0.999	0.000
C45 Mesothelioma	0.000	0.999	0.001
Q66 Congenital deformities of feet	0.000	0.999	0.001
S42.41 Fracture of lower end of humerus (open)	0.000	0.999	0.001
C26.9 Ill-defined sites within the digestive system	0.001	0.999	0.000
G40.6 Grand mal seizures, unspecified (with or without petit mal)	0.001	0.999	0.000
N60.1 Diffuse cystic mastopathy	0.001	0.999	0.000
Q65.9 Congenital deformity of hip, unspecified	0.000	0.999	0.001
Q65.6 Unstable hip	0.000	0.999	0.001
Q65.5 Congenital subluxation of hip, unspecified	0.000	0.999	0.001
Q65.4 Congenital subluxation of hip, bilateral	0.000	0.999	0.001
Q65.3 Congenital subluxation of hip, unilateral	0.000	0.999	0.001
Q65.2 Congenital dislocation of hip, unspecified	0.000	0.999	0.001
Q65.1 Congenital dislocation of hip, bilateral	0.000	0.999	0.001
Q65.0 Congenital dislocation of hip, unilateral	0.000	0.999	0.001
S42.1 Fracture of scapula	0.000	0.999	0.001
Y49.5 Other antipsychotics and neuroleptics	0.001	0.999	0.000
O36 Maternal care for other known or suspected foetal problems	0.000	0.999	0.001
M65.92 Synovitis and tenosynovitis, unspecified (Upper arm)	0.001	0.999	0.000
C17.8 Overlapping lesion of small intestine	0.001	0.999	0.000
C17.3 Meckel's diverticulum	0.001	0.999	0.000
C17.1 Jejunum	0.001	0.999	0.000
C34.0 Main bronchus	0.000	0.999	0.001
D75.9 Disease of blood and blood-forming organs, unspecified	0.001	0.999	0.000
M65.8 Other synovitis and tenosynovitis	0.001	0.999	0.000
Q12.9 Congenital lens malformation, unspecified	0.000	0.999	0.001
Q12.8 Other congenital lens malformations	0.000	0.999	0.001
Q12.4 Spherophakia	0.000	0.999	0.001
Q12.3 Congenital aphakia	0.000	0.999	0.001
Q12.2 Coloboma of lens	0.000	0.999	0.001

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

The full results table can be downloaded from this page.

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

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

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

Variant-specific associations