TreeWAS – Variant ID: rs7705033

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
U80 Agent resistant to penicillin and related antibiotics	0.162	0.838	0.000
U80.1 Methicillin resistant agent	0.161	0.839	0.000
U80.0 Penicillin resistant agent	0.157	0.843	0.000
U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use	0.140	0.860	0.000
U80.8 Agent resistant to other penicillin-related antibiotic	0.138	0.862	0.000
U51 Admission status on psychiatric patients	0.120	0.880	0.000
Chapter XXII Codes for special purposes	0.113	0.887	0.000
U51.0 Not Previously admitted to a psyciatric hospital	0.111	0.889	0.000
U82-U85 Resistance to antimicrobial and antineoplastic drugs	0.109	0.891	0.000
U89 Agent resistant to other and unspecified antibiotics	0.108	0.892	0.000
U89.8 Agent resistant to other single specified antibiotic	0.107	0.893	0.000
U50 Level of care administered to neonates	0.101	0.899	0.000
U07 Emergency use of U07	0.101	0.899	0.000
U06 Emergency use of U06	0.101	0.899	0.000
U04 Severe acute respiratory syndrome [SARS]	0.101	0.899	0.000
U52 First in a series of a regular day/night admissions	0.101	0.899	0.000
U81 Agent resistant to vancomycin and related antibiotics	0.095	0.905	0.000
U51.2 Previously admitted to a psychiatric hospital of another provider	0.093	0.907	0.000
U89.9 Agent resistant to unspecified antibiotic	0.081	0.919	0.000
M79.62 Pain in limb (Upper arm)	0.079	0.921	0.000
U84 Resistance to other antimicrobial drugs	0.078	0.922	0.000
U83 Resistance to other antibiotics	0.078	0.922	0.000
U82 Resistance to betalactam antibiotics	0.078	0.922	0.000
U85 Resistance to antineoplastic drugs	0.078	0.922	0.000
U04.9 Severe acute respiratory syndrome [SARS], unspecified	0.072	0.927	0.000
U06.9 Emergency use of U06.9	0.072	0.927	0.000
U06.8 Emergency use of U06.8	0.072	0.927	0.000
U06.7 Emergency use of U06.7	0.072	0.927	0.000
U06.6 Emergency use of U06.6	0.072	0.927	0.000
U06.5 Emergency use of U06.5	0.072	0.927	0.000
U06.4 Emergency use of U06.4	0.072	0.927	0.000
U06.3 Emergency use of U06.3	0.072	0.927	0.000
U06.2 Emergency use of U06.2	0.072	0.927	0.000
U06.1 Emergency use of U06.1	0.072	0.927	0.000
U06.0 Emergency use of U06.0	0.072	0.927	0.000
U07.9 Emergency use of U07.9	0.072	0.927	0.000
U07.8 Emergency use of U07.8	0.072	0.927	0.000
U07.7 Emergency use of U07.7	0.072	0.927	0.000
U07.6 Emergency use of U07.6	0.072	0.927	0.000
U07.5 Emergency use of U07.5	0.072	0.927	0.000
U07.4 Emergency use of U07.4	0.072	0.927	0.000
U07.3 Emergency use of U07.3	0.072	0.927	0.000
U07.2 Emergency use of U07.2	0.072	0.927	0.000
U07.1 Emergency use of U07.1	0.072	0.927	0.000
U07.0 Emergency use of U07.0	0.072	0.927	0.000
U50.9 Inquest Adjourned Death	0.072	0.927	0.000
U50.3 Level of care administered to neonates (Maximal Intensive Care)	0.072	0.927	0.000
U50.2 Level of care administered to neonates (High Dependancy Intensive Care)	0.072	0.927	0.000
U50.1 Level of care administered to neonates (Special Care)	0.072	0.927	0.000
U50.0 Level of care administered to neonates (Normal Care)	0.072	0.927	0.000
U81.8 Agent resistant to other vancomycin-related antibiotic	0.068	0.931	0.000
U88 Agent resistant to multiple antibiotics	0.067	0.933	0.000
U81.0 Vancomycin resistant agent	0.063	0.937	0.000
U82.9 Resistance to betalactam antibiotics, unspecified	0.056	0.944	0.000
U82.8 Resistance to other betalactam antibiotics	0.056	0.944	0.000
U82.2 Extended spectrum betalactamase (ESBL) resistance	0.056	0.944	0.000
U82.1 Resistance to methicillin	0.056	0.944	0.000
U82.0 Resistance to penicillin	0.056	0.944	0.000
U83.9 Resistance to unspecified antibiotic	0.056	0.944	0.000
U83.8 Resistance to other single specified antibiotic	0.056	0.944	0.000
U83.7 Resistance to multiple antibiotics	0.056	0.944	0.000
U83.2 Resistance to quinolones	0.056	0.944	0.000
U83.1 Resistance to other vancomycin related antibiotics	0.056	0.944	0.000
U83.0 Resistance to vancomycin	0.056	0.944	0.000
U84.9 Resistance to unspecified antimicrobial drugs	0.056	0.944	0.000
U84.8 Resistance to other specified antimicrobial drug	0.056	0.944	0.000
U84.7 Resistance to multiple antimicrobial drugs	0.056	0.944	0.000
U84.3 Resistance to tuberculostatic drug(s)	0.056	0.944	0.000
U84.2 Resistance to antiviral drug(s)	0.056	0.944	0.000
U84.1 Resistance to antifungal drug(s)	0.056	0.944	0.000
U84.0 Resistance to antiparasitic drug(s)	0.056	0.944	0.000
U51.1 Previously admitted to a psychiatric hospital of the provider	0.056	0.944	0.000
M79.60 Pain in limb (Multiple sites)	0.029	0.971	0.000
M79.6 Pain in limb	0.028	0.972	0.000
M79.63 Pain in limb (Forearm)	0.026	0.974	0.000
M79.61 Pain in limb (Shoulder region)	0.023	0.977	0.000
M79.68 Pain in limb (Other)	0.020	0.980	0.000
Z95.0 Presence of cardiac pacemaker	0.000	0.981	0.019
M79.64 Pain in limb (Hand)	0.019	0.981	0.000
M79.69 Pain in limb (Site unspecified)	0.015	0.985	0.000
R87.6 Abnormal cytological findings	0.011	0.989	0.000
M79.66 Pain in limb (Lower leg)	0.010	0.990	0.000
A87.9 Viral meningitis, unspecified	0.009	0.991	0.000
Y83.3 Surgical operation with formation of external stoma	0.008	0.992	0.000
D86.8 Sarcoidosis of other and combined sites	0.007	0.993	0.000
R87 Abnormal findings in specimens from female genital organs	0.007	0.993	0.000
Q21.1 Atrial septal defect	0.006	0.994	0.000
I12.0 Hypertensive renal disease with renal failure	0.000	0.994	0.006
K86.8 Other specified diseases of pancreas	0.006	0.994	0.000
R87.9 Unspecified abnormal finding	0.006	0.994	0.000
M06.99 Rheumatoid arthritis, unspecified (Site unspecified)	0.006	0.994	0.000
Q21 Congenital malformations of cardiac septa	0.006	0.994	0.000
M79.65 Pain in limb (Pelvic region and thigh)	0.005	0.995	0.000
R87.8 Other abnormal findings	0.005	0.995	0.000
R87.5 Abnormal microbiological findings	0.005	0.995	0.000
R87.4 Abnormal immunological findings	0.005	0.995	0.000
R87.3 Abnormal level of substances chiefly nonmedicinal as to source	0.005	0.995	0.000
R87.2 Abnormal level of other drugs, medicaments and biological substances	0.005	0.995	0.000
R87.1 Abnormal level of hormones	0.005	0.995	0.000
R87.0 Abnormal level of enzymes	0.005	0.995	0.000
Q21.0 Ventricular septal defect	0.005	0.995	0.000
M23.33 Other meniscus derangements (Medial collateral ligament or Other and unspecified medial meniscus)	0.005	0.995	0.000
Q21.8 Other congenital malformations of cardiac septa	0.005	0.995	0.000
A87 Viral meningitis	0.004	0.995	0.000
R87.7 Abnormal histological findings	0.004	0.996	0.000
N35.9 Urethral stricture, unspecified	0.004	0.996	0.000
Q21.3 Tetralogy of Fallot	0.004	0.996	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.004	0.996	0.000
Q21.4 Aortopulmonary septal defect	0.004	0.996	0.000
Q21.2 Atrioventricular septal defect	0.004	0.996	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.004	0.996	0.000
Q25 Congenital malformations of great arteries	0.004	0.996	0.000
Q25.1 Coarctation of aorta	0.004	0.996	0.000
D86 Sarcoidosis	0.004	0.996	0.000
Q39.6 Diverticulum of oesophagus	0.004	0.996	0.000
D41.4 Bladder	0.000	0.996	0.004
A87.8 Other viral meningitis	0.003	0.996	0.000
A87.2 Lymphocytic choriomeningitis	0.003	0.996	0.000
A87.1 Adenoviral meningitis	0.003	0.996	0.000
A87.0 Enteroviral meningitis	0.003	0.996	0.000
R47.0 Dysphasia and aphasia	0.003	0.997	0.000
Q24 Other congenital malformations of heart	0.003	0.997	0.000
D86.1 Sarcoidosis of lymph nodes	0.003	0.997	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.003	0.997	0.000
R19.0 Intra-abdominal and pelvic swelling, mass and lump	0.000	0.997	0.003
W07.0 Home	0.003	0.997	0.000
Q23 Congenital malformations of aortic and mitral valves	0.003	0.997	0.000
I12 Hypertensive renal disease	0.000	0.997	0.003
Q39 Congenital malformations of oesophagus	0.003	0.997	0.000
W07.9 Unspecified place	0.003	0.997	0.000
Q25.4 Other congenital malformations of aorta	0.003	0.997	0.000
Q24.5 Malformation of coronary vessels	0.003	0.997	0.000
D86.3 Sarcoidosis of skin	0.003	0.997	0.000
Q25.3 Stenosis of aorta	0.003	0.997	0.000
Q26 Congenital malformations of great veins	0.003	0.997	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.003	0.997	0.000
Q25.0 Patent ductus arteriosus	0.003	0.997	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.003	0.997	0.000
Q25.8 Other congenital malformations of great arteries	0.003	0.997	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.003	0.997	0.000
Q25.6 Stenosis of pulmonary artery	0.003	0.997	0.000
Q25.5 Atresia of pulmonary artery	0.003	0.997	0.000
Q25.2 Atresia of aorta	0.003	0.997	0.000
Q61.3 Polycystic kidney, unspecified	0.000	0.997	0.003
Z88.4 Personal history of allergy to anaesthetic agent	0.003	0.997	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.003	0.997	0.000
Q23.0 Congenital stenosis of aortic valve	0.003	0.997	0.000
Z43.3 Attention to colostomy	0.003	0.997	0.000
Q39.4 Oesophageal web	0.003	0.997	0.000
Z99.8 Dependence on other enabling machines and devices	0.003	0.997	0.000
T84.8 Other complications of internal orthopaedic prosthetic devices, implants and grafts	0.003	0.997	0.000
D69.6 Thrombocytopenia, unspecified	0.000	0.997	0.003
I12.9 Hypertensive renal disease without renal failure	0.000	0.997	0.003
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes	0.003	0.997	0.000
Q22.1 Congenital pulmonary valve stenosis	0.003	0.997	0.000
Z91.6 Personal history of other physical trauma	0.003	0.997	0.000
D80 Immunodeficiency with predominantly antibody defects	0.003	0.997	0.000
K14.0 Glossitis	0.000	0.997	0.003
D80.1 Nonfamilial hypogammaglobulinaemia	0.003	0.997	0.000
K58.0 Irritable bowel syndrome with diarrhoea	0.003	0.997	0.000
R47.1 Dysarthria and anarthria	0.003	0.997	0.000
Q24.6 Congenital heart block	0.003	0.997	0.000
Q24.4 Congenital subaortic stenosis	0.003	0.997	0.000
Q24.3 Pulmonary infundibular stenosis	0.003	0.997	0.000
Q24.2 Cor triatriatum	0.003	0.997	0.000
Q24.1 Levocardia	0.003	0.997	0.000
Q24.0 Dextrocardia	0.003	0.997	0.000
D80-D89 Certain disorders involving the immune mechanism	0.003	0.997	0.000
M79.67 Pain in limb (Ankle and foot)	0.002	0.997	0.001
D23.1 Skin of eyelid, including canthus	0.000	0.997	0.003
Q38-Q45 Other congenital malformations of the digestive system	0.003	0.997	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.003	0.997	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.003	0.997	0.000
Q22.6 Hypoplastic right heart syndrome	0.003	0.997	0.000
Q22.5 Ebstein's anomaly	0.003	0.997	0.000
Q22.4 Congenital tricuspid stenosis	0.003	0.997	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.003	0.997	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.003	0.997	0.000
Q22.0 Pulmonary valve atresia	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
G91.9 Hydrocephalus, unspecified	0.003	0.997	0.000
Q61.2 Polycystic kidney, adult type	0.000	0.997	0.003
Q39.9 Congenital malformation of oesophagus, unspecified	0.002	0.997	0.000
Q39.8 Other congenital malformations of oesophagus	0.002	0.997	0.000
Q39.5 Congenital dilatation of oesophagus	0.002	0.997	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.002	0.997	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.002	0.997	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.002	0.997	0.000
Q39.0 Atresia of oesophagus without fistula	0.002	0.997	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.003	0.997	0.000
W07 Fall involving chair	0.003	0.997	0.000
N02.8 Other	0.003	0.997	0.000
R83-R89 Abnormal findings on examination of other body fluids, substances and tissues, without diagnosis	0.003	0.997	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.002	0.997	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.002	0.997	0.000
Q20.6 Isomerism of atrial appendages	0.002	0.997	0.000
Q20.5 Discordant atrioventricular connexion	0.002	0.997	0.000
Q20.4 Double inlet ventricle	0.002	0.997	0.000
Q20.3 Discordant ventriculoarterial connexion	0.002	0.997	0.000
Q20.2 Double outlet left ventricle	0.002	0.997	0.000
Q20.1 Double outlet right ventricle	0.002	0.997	0.000
Q20.0 Common arterial trunk	0.002	0.997	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.002	0.997	0.000
Q26.8 Other congenital malformations of great veins	0.002	0.997	0.000
Q26.6 Portal vein-hepatic artery fistula	0.002	0.997	0.000
Q26.5 Anomalous portal venous connexion	0.002	0.997	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.002	0.997	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.002	0.997	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.002	0.997	0.000
Q26.1 Persistent left superior vena cava	0.002	0.997	0.000
Q26.0 Congenital stenosis of vena cava	0.002	0.997	0.000
R47 Speech disturbances, not elsewhere classified	0.003	0.997	0.000
N05.9 Unspecified	0.003	0.997	0.000
R45.8 Other symptoms and signs involving emotional state	0.000	0.997	0.003
M62.81 Other specified disorders of muscle (Shoulder region)	0.002	0.997	0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.002	0.997	0.000
R89 Abnormal findings in specimens from other organs, systems and tissues	0.002	0.997	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.997	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.997	0.000
D69.3 Idiopathic thrombocytopenic purpura	0.000	0.998	0.002
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
Q65.8 Other congenital deformities of hip	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q65 Congenital deformities of hip	0.002	0.998	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.002	0.998	0.000
R89.7 Abnormal histological findings	0.002	0.998	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.002	0.998	0.000
N02.2 Diffuse membranous glomerulonephritis	0.002	0.998	0.000
M24.66 Ankylosis of joint (Lower leg)	0.002	0.998	0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]	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
D80.0 Hereditary hypogammaglobulinaemia	0.002	0.998	0.000
M62.82 Other specified disorders of muscle (Upper arm)	0.002	0.998	0.000
Q79.0 Congenital diaphragmatic hernia	0.002	0.998	0.000
Q38.1 Ankyloglossia	0.002	0.998	0.000
D84 Other immunodeficiencies	0.002	0.998	0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.002	0.998	0.000
F45.8 Other somatoform disorders	0.002	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
Q44.6 Cystic disease of liver	0.000	0.998	0.002
Q61 Cystic kidney disease	0.000	0.998	0.002
H34.8 Other retinal vascular occlusions	0.002	0.998	0.000
H93.1 Tinnitus	0.000	0.998	0.002
K70.0 Alcoholic fatty liver	0.000	0.998	0.002
Q79.8 Other congenital malformations of musculoskeletal system	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
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
Q23.1 Congenital insufficiency of aortic valve	0.002	0.998	0.000
N02 Recurrent and persistent haematuria	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.002	0.998	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.001	0.998	0.001
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
T11.1 Open wound of upper limb, level unspecified	0.002	0.998	0.000
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
Q38.4 Congenital malformations of salivary glands and ducts	0.002	0.998	0.000
Q38.3 Other congenital malformations of tongue	0.002	0.998	0.000
Q38.2 Macroglossia	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
R89.5 Abnormal microbiological findings	0.002	0.998	0.000
D83 Common variable immunodeficiency	0.002	0.998	0.000
K11.1 Hypertrophy of salivary gland	0.000	0.998	0.002
W07.2 School, other institution and public administrative area	0.002	0.998	0.000
W07.8 Other specified place	0.002	0.998	0.000
W07.7 Farm	0.002	0.998	0.000
W07.6 Industrial and construction area	0.002	0.998	0.000
W07.4 Street and highway	0.002	0.998	0.000
W07.3 Sports and athletics area	0.002	0.998	0.000
W07.1 Residential institution	0.002	0.998	0.000
D61.9 Aplastic anaemia, unspecified	0.000	0.998	0.002
D69 Purpura and other haemorrhagic conditions	0.000	0.998	0.002
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
T14 Injury of unspecified body region	0.002	0.998	0.000
Q79.6 Ehlers-Danlos syndrome	0.002	0.998	0.000
N92.4 Excessive bleeding in the premenopausal period	0.002	0.998	0.000
R84 Abnormal findings in specimens from respiratory organs and thorax	0.002	0.998	0.000
R86.9 Unspecified abnormal finding	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
D89.1 Cryoglobulinaemia	0.002	0.998	0.000
N02.0 Minor glomerular abnormality	0.002	0.998	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.002	0.998	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.002	0.998	0.000
Q28.3 Other malformations of cerebral vessels	0.002	0.998	0.000
Q28.1 Other malformations of precerebral vessels	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.002	0.998	0.000
Q79.5 Other congenital malformations of abdominal wall	0.002	0.998	0.000
Q79.4 Prune belly syndrome	0.002	0.998	0.000
Q79.3 Gastroschisis	0.002	0.998	0.000
Q79.2 Exomphalos	0.002	0.998	0.000
Q79.1 Other congenital malformations of diaphragm	0.002	0.998	0.000
R89.9 Unspecified abnormal finding	0.002	0.998	0.000
R89.8 Other abnormal findings	0.002	0.998	0.000
R89.6 Abnormal cytological findings	0.002	0.998	0.000
R89.4 Abnormal immunological findings	0.002	0.998	0.000
R89.3 Abnormal level of substances chiefly nonmedicinal as to source	0.002	0.998	0.000
R89.2 Abnormal level of other drugs, medicaments and biological substances	0.002	0.998	0.000
R89.1 Abnormal level of hormones	0.002	0.998	0.000
R89.0 Abnormal level of enzymes	0.002	0.998	0.000
T14.9 Injury, unspecified	0.002	0.998	0.000
T14.0 Superficial injury of unspecified body region	0.002	0.998	0.000
R83 Abnormal findings in cerebrospinal fluid	0.002	0.998	0.000
K11.9 Disease of salivary gland, unspecified	0.000	0.998	0.002
R86 Abnormal findings in specimens from male genital organs	0.002	0.998	0.000
D84.1 Defects in the complement system	0.002	0.998	0.000
D89.3 Immune reconstitution syndrome	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.998	0.000
R44.1 Visual hallucinations	0.000	0.998	0.002
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.002	0.998	0.000
Q73 Reduction defects of unspecified limb	0.002	0.998	0.000
Q72 Reduction defects of lower limb	0.002	0.998	0.000
Q71 Reduction defects of upper limb	0.002	0.998	0.000
Q70 Syndactyly	0.002	0.998	0.000
Q69 Polydactyly	0.002	0.998	0.000
Q61.9 Cystic kidney disease, unspecified	0.000	0.998	0.002
W07.5 Trade and service area	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
M62.80 Other specified disorders of muscle (Multiple sites)	0.002	0.998	0.000
D69.2 Other nonthrombocytopenic purpura	0.000	0.998	0.002
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.002	0.998	0.000
Q27.4 Congenital phlebectasia	0.002	0.998	0.000
Q27.2 Other congenital malformations of renal artery	0.002	0.998	0.000
Q27.1 Congenital renal artery stenosis	0.002	0.998	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.002	0.998	0.000
Q65.9 Congenital deformity of hip, unspecified	0.002	0.998	0.000
Q65.6 Unstable hip	0.002	0.998	0.000
Q65.5 Congenital subluxation of hip, unspecified	0.002	0.998	0.000
Q65.4 Congenital subluxation of hip, bilateral	0.002	0.998	0.000
Q65.3 Congenital subluxation of hip, unilateral	0.002	0.998	0.000
Q65.2 Congenital dislocation of hip, unspecified	0.002	0.998	0.000
Q65.1 Congenital dislocation of hip, bilateral	0.002	0.998	0.000
Q65.0 Congenital dislocation of hip, unilateral	0.002	0.998	0.000
Q66 Congenital deformities of feet	0.002	0.998	0.000
D84.8 Other specified immunodeficiencies	0.002	0.998	0.000
M62.8 Other specified disorders of muscle	0.002	0.998	0.000
O47.1 False labour at or after 37 completed weeks of gestation	0.002	0.998	0.000
O99.8 Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium	0.000	0.998	0.002
Q24.8 Other specified congenital malformations of heart	0.002	0.998	0.000
R84.7 Abnormal histological findings	0.002	0.998	0.000
T14.6 Injury of tendons and muscles of unspecified body region	0.002	0.998	0.000
T11 Other injuries of upper limb, level unspecified	0.002	0.998	0.000
T08-T14 Injuries to unspecified part of trunk, limb or body region	0.002	0.998	0.000
H00.1 Chalazion	0.000	0.998	0.002
Q31 Congenital malformations of larynx	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
J11.1 Influenza with other respiratory manifestations, virus not identified	0.000	0.998	0.002
K11.5 Sialolithiasis	0.000	0.998	0.002
Q78.0 Osteogenesis imperfecta	0.002	0.998	0.000
T13 Other injuries of lower limb, level unspecified	0.002	0.998	0.000
T08 Fracture of spine, level unspecified	0.002	0.998	0.000
D84.0 Lymphocyte function antigen-1 [LFA-1] defect	0.002	0.998	0.000
Q31.0 Web of larynx	0.002	0.998	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.002	0.998	0.000
Q78.2 Osteopetrosis	0.002	0.998	0.000
T81.7 Vascular complications following a procedure, not elsewhere classified	0.002	0.998	0.000
T09 Other injuries of spine and trunk, level unspecified	0.002	0.998	0.000
Q61.8 Other cystic kidney diseases	0.000	0.998	0.002
Q61.1 Polycystic kidney, infantile type	0.000	0.998	0.002
Q66.7 Pes cavus	0.002	0.998	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
D69.0 Allergic purpura	0.000	0.998	0.002
D81.9 Combined immunodeficiency, unspecified	0.002	0.998	0.000
D81.8 Other combined immunodeficiencies	0.002	0.998	0.000
D81.7 Major histocompatibility complex class II deficiency	0.002	0.998	0.000
D81.6 Major histocompatibility complex class I deficiency	0.002	0.998	0.000
D81.5 Purine nucleoside phosphorylase [PNP] deficiency	0.002	0.998	0.000
D81.4 Nezelof's syndrome	0.002	0.998	0.000
D81.3 Adenosine deaminase [ADA] deficiency	0.002	0.998	0.000
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers	0.002	0.998	0.000
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers	0.002	0.998	0.000
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis	0.002	0.998	0.000
D82.9 Immunodeficiency associated with major defect, unspecified	0.002	0.998	0.000
D82.8 Immunodeficiency associated with other specified major defects	0.002	0.998	0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome	0.002	0.998	0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus	0.002	0.998	0.000
D82.2 Immunodeficiency with short-limbed stature	0.002	0.998	0.000
D82.1 Di George's syndrome	0.002	0.998	0.000
D82.0 Wiskott-Aldrich syndrome	0.002	0.998	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.002	0.998	0.000
R47.8 Other and unspecified speech disturbances	0.002	0.998	0.000
K11.2 Sialoadenitis	0.000	0.998	0.002
N02.7 Diffuse crescentic glomerulonephritis	0.002	0.998	0.000
N02.6 Dense deposit disease	0.002	0.998	0.000
N02.5 Diffuse mesangiocapillary glomerulonephritis	0.002	0.998	0.000
N02.4 Diffuse endocapillary proliferative glomerulonephritis	0.002	0.998	0.000
N02.3 Diffuse mesangial proliferative glomerulonephritis	0.002	0.998	0.000
N02.1 Focal and segmental glomerular lesions	0.002	0.998	0.000
N93.9 Abnormal uterine and vaginal bleeding, unspecified	0.002	0.998	0.000
Q07.8 Other specified congenital malformations of nervous system	0.002	0.998	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.002	0.998	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.002	0.998	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.002	0.998	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.002	0.998	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.002	0.998	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.002	0.998	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.002	0.998	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.002	0.998	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.002	0.998	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.002	0.998	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.002	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.002	0.998	0.000
Q45.8 Other specified congenital malformations of digestive system	0.002	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.002	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.002	0.998	0.000
Q45.1 Annular pancreas	0.002	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.002	0.998	0.000
T09.0 Superficial injury of trunk, level unspecified	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	0.001	0.998	0.001
Q44.4 Choledochal cyst	0.001	0.998	0.001
Q44.3 Congenital stenosis and stricture of bile ducts	0.001	0.998	0.001
Q44.2 Atresia of bile ducts	0.001	0.998	0.001
Q44.1 Other congenital malformations of gallbladder	0.001	0.998	0.001
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.001	0.998	0.001
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
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
M35.0 Sicca syndrome [Sjogren]	0.002	0.998	0.000
Q07.0 Arnold-Chiari syndrome	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
W07.29 Fall involving chair; School, other institution and public administrative area; During unspecified activity	0.002	0.998	0.000
D69.4 Other primary thrombocytopenia	0.000	0.998	0.002
D89.0 Polyclonal hypergammaglobulinaemia	0.002	0.998	0.000
G91.2 Normal-pressure hydrocephalus	0.002	0.998	0.000
M22.4 Chondromalacia patellae	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.001	0.998	0.001
Q68.5 Congenital bowing of long bones of leg, unspecified	0.002	0.998	0.000
Q68.4 Congenital bowing of tibia and fibula	0.002	0.998	0.000
Q68.3 Congenital bowing of femur	0.002	0.998	0.000
Q68.2 Congenital deformity of knee	0.002	0.998	0.000
Q68.1 Congenital deformity of hand	0.002	0.998	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.002	0.998	0.000
G91 Hydrocephalus	0.002	0.998	0.000
C24.0 Extrahepatic bile duct	0.002	0.998	0.000
D69.8 Other specified haemorrhagic conditions	0.000	0.998	0.002
F60.9 Personality disorder, unspecified	0.002	0.998	0.000
T14.2 Fracture of unspecified body region	0.002	0.998	0.000
T14.8 Other injuries of unspecified body region	0.002	0.998	0.000
T14.7 Crushing injury and traumatic amputation of unspecified body region	0.002	0.998	0.000
T14.5 Injury of blood vessel(s) of unspecified body region	0.002	0.998	0.000
T14.4 Injury of nerve(s) of unspecified body region	0.002	0.998	0.000
T14.3 Dislocation, sprain and strain of unspecified body region	0.002	0.998	0.000
Q66.9 Congenital deformity of feet, unspecified	0.002	0.998	0.000
R86.0 Abnormal level of enzymes	0.002	0.998	0.000
K11 Diseases of salivary glands	0.000	0.998	0.002
N05 Unspecified nephritic syndrome	0.002	0.998	0.000
K12.3 Oral mucositis (ulcerative)	0.000	0.998	0.002
R84.9 Unspecified abnormal finding	0.002	0.998	0.000
R84.8 Other abnormal findings	0.002	0.998	0.000
R84.6 Abnormal cytological findings	0.002	0.998	0.000
R84.4 Abnormal immunological findings	0.002	0.998	0.000
R84.3 Abnormal level of substances chiefly nonmedicinal as to source	0.002	0.998	0.000
R84.2 Abnormal level of other drugs, medicaments and biological substances	0.002	0.998	0.000
R84.1 Abnormal level of hormones	0.002	0.998	0.000
R84.0 Abnormal level of enzymes	0.002	0.998	0.000
T13.1 Open wound of lower limb, level unspecified	0.002	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.002	0.998	0.000
Q03 Congenital hydrocephalus	0.002	0.998	0.000
Q01 Encephalocele	0.002	0.998	0.000
Q00 Anencephaly and similar malformations	0.002	0.998	0.000
Q02 Microcephaly	0.002	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.002	0.998	0.000
Q33 Congenital malformations of lung	0.002	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.002	0.998	0.000
Q30 Congenital malformations of nose	0.002	0.998	0.000
G91.1 Obstructive hydrocephalus	0.002	0.998	0.000
Q61.4 Renal dysplasia	0.000	0.998	0.001
R83.9 Unspecified abnormal finding	0.002	0.998	0.000
R83.7 Abnormal histological findings	0.002	0.998	0.000
R83.6 Abnormal cytological findings	0.002	0.998	0.000
R83.5 Abnormal microbiological findings	0.002	0.998	0.000

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

The full results table can be downloaded from this page.

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

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

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

Variant-specific associations