TreeWAS – Variant ID: rs12269901

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
G43.9 Migraine, unspecified	0.000	0.966	0.034
M34.9 Systemic sclerosis, unspecified	0.019	0.981	0.000
M34 Systemic sclerosis	0.015	0.985	0.000
N97.9 Female infertility, unspecified	0.000	0.986	0.014
O82.0 Delivery by elective Caesarean section	0.000	0.986	0.014
M34.1 CR(E)ST syndrome	0.014	0.986	0.000
G43 Migraine	0.000	0.986	0.014
M34.0 Progressive systemic sclerosis	0.012	0.988	0.000
G43.1 Migraine with aura [classical migraine]	0.000	0.989	0.011
M34.2 Systemic sclerosis induced by drugs and chemicals	0.011	0.989	0.000
M34.8 Other forms of systemic sclerosis	0.011	0.989	0.000
S22.40 Multiple fractures of ribs (closed)	0.010	0.990	0.000
G43.2 Status migrainosus	0.000	0.990	0.010
G43.3 Complicated migraine	0.000	0.990	0.010
G43.0 Migraine without aura [common migraine]	0.000	0.991	0.009
I49.9 Cardiac arrhythmia, unspecified	0.009	0.991	0.000
O82 Single delivery by Caesarean section	0.000	0.991	0.009
G43.8 Other migraine	0.000	0.991	0.009
I87.2 Venous insufficiency (chronic) (peripheral)	0.009	0.991	0.000
J13 Pneumonia due to Streptococcus pneumoniae	0.000	0.992	0.008
O82.1 Delivery by emergency Caesarean section	0.000	0.993	0.007
O82.9 Delivery by Caesarean section, unspecified	0.000	0.993	0.007
K04.6 Periapical abscess with sinus	0.007	0.993	0.000
O82.8 Other single delivery by Caesarean section	0.000	0.993	0.007
O82.2 Delivery by Caesarean hysterectomy	0.000	0.993	0.007
I08.1 Disorders of both mitral and tricuspid valves	0.006	0.994	0.000
Z63.4 Disappearance and death of family member	0.006	0.994	0.000
M07.39 Other psoriatic arthropathies (Site unspecified)	0.000	0.994	0.006
Z63.0 Problems in relationship with spouse or partner	0.006	0.994	0.000
M22.8 Other disorders of patella	0.006	0.994	0.000
Z63 Other problems related to primary support group, including family circumstances	0.006	0.994	0.000
I87 Other disorders of veins	0.005	0.995	0.000
S22.4 Multiple fractures of ribs	0.005	0.995	0.000
Z63.8 Other specified problems related to primary support group	0.005	0.995	0.000
M80.10 Postoophorectomy osteoporosis with pathological fracture (Multiple sites)	0.005	0.995	0.000
E03.9 Hypothyroidism, unspecified	0.000	0.995	0.005
F60.9 Personality disorder, unspecified	0.000	0.995	0.005
I87.1 Compression of vein	0.005	0.995	0.000
O86.0 Infection of obstetric surgical wound	0.005	0.995	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.005	0.995	0.000
E03.8 Other specified hypothyroidism	0.000	0.995	0.005
S12.70 Multiple fractures of cervical spine (closed)	0.000	0.996	0.004
Q24 Other congenital malformations of heart	0.004	0.996	0.000
C53.9 Cervix uteri, unspecified	0.004	0.996	0.000
I87.9 Disorder of vein, unspecified	0.004	0.996	0.000
A87.9 Viral meningitis, unspecified	0.000	0.996	0.004
I87.8 Other specified disorders of veins	0.004	0.996	0.000
Z63.5 Disruption of family by separation and divorce	0.004	0.996	0.000
Z63.9 Problem related to primary support group, unspecified	0.004	0.996	0.000
Z63.3 Absence of family member	0.004	0.996	0.000
Z63.2 Inadequate family support	0.004	0.996	0.000
Z63.1 Problems in relationship with parents and in-laws	0.004	0.996	0.000
I87.0 Postphlebitic syndrome	0.004	0.996	0.000
N97 Female infertility	0.000	0.996	0.004
S22.41 Multiple fractures of ribs (open)	0.004	0.996	0.000
I12.0 Hypertensive renal disease with renal failure	0.000	0.996	0.004
Z88.2 Personal history of allergy to sulphonamides	0.000	0.996	0.004
Q24.8 Other specified congenital malformations of heart	0.004	0.996	0.000
M22 Disorders of patella	0.004	0.996	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.004	0.996	0.000
Z63.6 Dependent relative needing care at home	0.004	0.996	0.000
M79.09 Rheumatism, unspecified (Site unspecified)	0.000	0.996	0.004
Z57.2 Occupational exposure to dust	0.004	0.996	0.000
E03 Other hypothyroidism	0.000	0.996	0.004
K74.6 Other and unspecified cirrhosis of liver	0.004	0.996	0.000
F60 Specific personality disorders	0.000	0.996	0.004
Q24.6 Congenital heart block	0.004	0.996	0.000
M22.3 Other derangements of patella	0.004	0.996	0.000
Z80.9 Family history of malignant neoplasm, unspecified	0.000	0.996	0.004
Q38-Q45 Other congenital malformations of the digestive system	0.004	0.996	0.000
Z63.7 Other stressful life events affecting family and household	0.004	0.996	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.004	0.996	0.000
Q39 Congenital malformations of oesophagus	0.004	0.996	0.000
F60.3 Emotionally unstable personality disorder	0.000	0.996	0.004
I34.0 Mitral (valve) insufficiency	0.000	0.996	0.004
K82.4 Cholesterolosis of gallbladder	0.000	0.996	0.004
M22.4 Chondromalacia patellae	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
Q27 Other congenital malformations of peripheral vascular system	0.003	0.997	0.000
D03.7 Melanoma in situ of lower limb, including hip	0.000	0.997	0.003
Q39.4 Oesophageal web	0.003	0.997	0.000
M22.9 Disorder of patella, unspecified	0.003	0.997	0.000
Q22.1 Congenital pulmonary valve stenosis	0.003	0.997	0.000
S05.0 Injury of conjunctiva and corneal abrasion without mention of foreign body	0.003	0.997	0.000
N97.8 Female infertility of other origin	0.000	0.997	0.003
N97.3 Female infertility of cervical origin	0.000	0.997	0.003
N97.2 Female infertility of uterine origin	0.000	0.997	0.003
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.003	0.997	0.000
M25.61 Stiffness of joint, not elsewhere classified (Shoulder region)	0.003	0.997	0.000
M43.16 Spondylolisthesis (Lumbar region)	0.003	0.997	0.000
Q28 Other congenital malformations of circulatory system	0.003	0.997	0.000
Q25 Congenital malformations of great arteries	0.003	0.997	0.000
Q24.5 Malformation of coronary vessels	0.003	0.997	0.000
S12.7 Multiple fractures of cervical spine	0.000	0.997	0.003
M43.17 Spondylolisthesis (Lumbosacral region)	0.003	0.997	0.000
J14 Pneumonia due to Haemophilus influenzae	0.000	0.997	0.003
Z57 Occupational exposure to risk-factors	0.003	0.997	0.000
Q43 Other congenital malformations of intestine	0.003	0.997	0.000
Q40 Other congenital malformations of upper alimentary tract	0.003	0.997	0.000
M22.1 Recurrent subluxation of patella	0.003	0.997	0.000
N97.4 Female infertility associated with male factors	0.000	0.997	0.003
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
N97.0 Female infertility associated with anovulation	0.000	0.997	0.003
Q39.6 Diverticulum of oesophagus	0.003	0.997	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.003	0.997	0.000
D03.3 Melanoma in situ of other and unspecified parts of face	0.000	0.997	0.003
O80-O84 Delivery	0.000	0.997	0.003
M07.3 Other psoriatic arthropathies	0.000	0.997	0.003
F60.0 Paranoid personality disorder	0.000	0.997	0.003
Q45 Other congenital malformations of digestive system	0.003	0.997	0.000
E03.5 Myxoedema coma	0.000	0.997	0.003
E03.4 Atrophy of thyroid (acquired)	0.000	0.997	0.003
E03.3 Postinfectious hypothyroidism	0.000	0.997	0.003
E03.1 Congenital hypothyroidism without goitre	0.000	0.997	0.003
M43.1 Spondylolisthesis	0.003	0.997	0.000
Q23 Congenital malformations of aortic and mitral valves	0.003	0.997	0.000
M21.37 Wrist or foot drop (acquired) (Ankle and foot)	0.003	0.997	0.000
Q43.0 Meckel's diverticulum	0.003	0.997	0.000
F60.7 Dependent personality disorder	0.000	0.997	0.003
Q96 Turner's syndrome	0.003	0.997	0.000
Q90 Down's syndrome	0.003	0.997	0.000
F60.4 Histrionic personality disorder	0.000	0.997	0.003
F60.2 Dissocial personality disorder	0.000	0.997	0.003
F60.1 Schizoid personality disorder	0.000	0.997	0.003
M21.17 Varus deformity, not elsewhere classified (Ankle and foot)	0.003	0.997	0.000
E03.2 Hypothyroidism due to medicaments and other exogenous substances	0.000	0.997	0.003
F60.5 Anankastic personality disorder	0.000	0.997	0.003
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.003	0.997	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.003	0.997	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.003	0.997	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.003	0.997	0.000
I83.1 Varicose veins of lower extremities with inflammation	0.000	0.997	0.003
Q43.3 Congenital malformations of intestinal fixation	0.003	0.997	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.003	0.997	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.003	0.997	0.000
F60.8 Other specific personality disorders	0.000	0.997	0.003
I08.0 Disorders of both mitral and aortic valves	0.003	0.997	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.003	0.997	0.000
M21.1 Varus deformity, not elsewhere classified	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
Q39.9 Congenital malformation of oesophagus, unspecified	0.003	0.997	0.000
Q39.8 Other congenital malformations of oesophagus	0.003	0.997	0.000
Q39.5 Congenital dilatation of oesophagus	0.003	0.997	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.003	0.997	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.003	0.997	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.003	0.997	0.000
Q39.0 Atresia of oesophagus without fistula	0.003	0.997	0.000
I08 Multiple valve diseases	0.003	0.997	0.000
M07.30 Other psoriatic arthropathies (Multiple sites)	0.000	0.997	0.003
M21.16 Varus deformity, not elsewhere classified (Lower leg)	0.003	0.997	0.000
M22.0 Recurrent dislocation of patella	0.003	0.997	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.003	0.997	0.000
S05.6 Penetrating wound of eyeball without foreign body	0.003	0.997	0.000
O81 Single delivery by forceps and vacuum extractor	0.000	0.997	0.003
S05 Injury of eye and orbit	0.003	0.997	0.000
F60.6 Anxious [avoidant] personality disorder	0.000	0.997	0.003
M80.1 Postoophorectomy osteoporosis with pathological fracture	0.003	0.997	0.000
Q90.9 Down's syndrome, unspecified	0.003	0.997	0.000
Q96.9 Turner's syndrome, unspecified	0.003	0.997	0.000
Q27.4 Congenital phlebectasia	0.003	0.997	0.000
Q27.2 Other congenital malformations of renal artery	0.003	0.997	0.000
Q27.1 Congenital renal artery stenosis	0.003	0.997	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.003	0.997	0.000
D03 Melanoma in situ	0.000	0.997	0.003
Q25.4 Other congenital malformations of aorta	0.003	0.997	0.000
Q40.2 Other specified congenital malformations of stomach	0.003	0.997	0.000
K74 Fibrosis and cirrhosis of liver	0.003	0.997	0.000
Q27.3 Peripheral arteriovenous malformation	0.003	0.997	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.003	0.997	0.000
Z57.5 Occupational exposure to toxic agents in other industries	0.003	0.997	0.000
Z61 Problems related to negative life events in childhood	0.003	0.997	0.000
Z57.3 Occupational exposure to other air contaminants	0.003	0.997	0.000
Q25.0 Patent ductus arteriosus	0.003	0.997	0.000
Q44.5 Other congenital malformations of bile ducts	0.003	0.997	0.000
Q99.8 Other specified chromosome abnormalities	0.003	0.997	0.000
M43.12 Spondylolisthesis (Cervical region)	0.003	0.997	0.000
N97.1 Female infertility of tubal origin	0.000	0.997	0.003
S05.3 Ocular laceration without prolapse or loss of intraocular tissue	0.003	0.997	0.000
Z61.6 Problems related to alleged physical abuse of child	0.003	0.997	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.003	0.997	0.000
Z55-Z65 Persons with potential health hazards related to socioeconomic and psychosocial circumstances	0.003	0.997	0.000
E03.0 Congenital hypothyroidism with diffuse goitre	0.000	0.997	0.002
K74.5 Biliary cirrhosis, unspecified	0.003	0.997	0.000
O81.3 Other and unspecified forceps delivery	0.000	0.997	0.003
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.002	0.997	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.002	0.997	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.002	0.997	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.002	0.997	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.002	0.997	0.000
N87.0 Mild cervical dysplasia	0.003	0.997	0.000
Q40.1 Congenital hiatus hernia	0.002	0.997	0.000
Y57.5 X-ray contrast media	0.003	0.997	0.000
M21.3 Wrist or foot drop (acquired)	0.003	0.997	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.002	0.997	0.000
Q25.8 Other congenital malformations of great arteries	0.002	0.997	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.997	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.997	0.000
Q25.3 Stenosis of aorta	0.002	0.997	0.000
Q25.2 Atresia of aorta	0.002	0.997	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.002	0.997	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.002	0.997	0.000
Q28.3 Other malformations of cerebral vessels	0.002	0.997	0.000
Q28.1 Other malformations of precerebral vessels	0.002	0.997	0.000
Q43.1 Hirschsprung's disease	0.002	0.997	0.000
Q25.6 Stenosis of pulmonary artery	0.002	0.997	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.997	0.000
S12.71 Multiple fractures of cervical spine (open)	0.000	0.997	0.002
D03.5 Melanoma in situ of trunk	0.000	0.997	0.003
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.997	0.000
Q45.8 Other specified congenital malformations of digestive system	0.002	0.997	0.000
S05.9 Injury of eye and orbit, part unspecified	0.003	0.997	0.000
Q14 Congenital malformations of posterior segment of eye	0.002	0.997	0.000
K91.8 Other postprocedural disorders of digestive system, not elsewhere classified	0.003	0.997	0.000
Z57.9 Occupational exposure to unspecified risk-factor	0.002	0.997	0.000
Z57.7 Occupational exposure to vibration	0.002	0.997	0.000
Z57.6 Occupational exposure to extreme temperature	0.002	0.997	0.000
Z57.4 Occupational exposure to toxic agents in agriculture	0.002	0.997	0.000
Z57.1 Occupational exposure to radiation	0.002	0.997	0.000
Z57.0 Occupational exposure to noise	0.002	0.997	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.997	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.997	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.997	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.997	0.000
Q43.7 Persistent cloaca	0.002	0.997	0.000
Q43.6 Congenital fistula of rectum and anus	0.002	0.997	0.000
Q43.5 Ectopic anus	0.002	0.997	0.000
Q43.4 Duplication of intestine	0.002	0.997	0.000
Q43.2 Other congenital functional disorders of colon	0.002	0.997	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.997	0.000
M22.10 Recurrent subluxation of patella, unspecified knee	0.002	0.997	0.000
D03.4 Melanoma in situ of scalp and neck	0.000	0.997	0.002
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
Q14.1 Congenital malformation of retina	0.002	0.997	0.000
Q38.6 Other congenital malformations of mouth	0.002	0.997	0.000
Q38.1 Ankyloglossia	0.002	0.997	0.000
O84 Multiple delivery	0.000	0.997	0.002
O83 Other assisted single delivery	0.000	0.997	0.002
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.997	0.000
G47.0 Disorders of initiating and maintaining sleep [insomnias]	0.002	0.997	0.000
Q25.1 Coarctation of aorta	0.002	0.997	0.000
S05.1 Contusion of eyeball and orbital tissues	0.002	0.997	0.000
Q60-Q64 Congenital malformations of the urinary system	0.002	0.997	0.000
M07.38 Other psoriatic arthropathies (Other)	0.000	0.998	0.002
M07.35 Other psoriatic arthropathies (Pelvic region and thigh)	0.000	0.998	0.002
M07.33 Other psoriatic arthropathies (Forearm)	0.000	0.998	0.002
M07.32 Other psoriatic arthropathies (Upper arm)	0.000	0.998	0.002
M07.31 Other psoriatic arthropathies (Shoulder region)	0.000	0.998	0.002
Q23.1 Congenital insufficiency of aortic valve	0.002	0.998	0.000
Q28.2 Arteriovenous malformation of cerebral vessels	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
M22.2 Patellofemoral disorders	0.002	0.998	0.000
Q45.9 Congenital malformation of digestive system, unspecified	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
M07.34 Other psoriatic arthropathies (Hand)	0.000	0.998	0.002
M43.18 Spondylolisthesis (Sacral and sacrococcygeal region)	0.002	0.998	0.000
M43.15 Spondylolisthesis (Thoracolumbar region)	0.002	0.998	0.000
M43.14 Spondylolisthesis (Thoracic region)	0.002	0.998	0.000
M43.13 Spondylolisthesis (Cervicothoracic region)	0.002	0.998	0.000
M43.11 Spondylolisthesis (Occipito-atlanto-axial region)	0.002	0.998	0.000
M43.10 Spondylolisthesis (Multiple sites in spine)	0.002	0.998	0.000
K74.0 Hepatic fibrosis	0.002	0.998	0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.002	0.998	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q23.4 Hypoplastic left heart syndrome	0.002	0.998	0.000
Q23.3 Congenital mitral insufficiency	0.002	0.998	0.000
Q23.2 Congenital mitral stenosis	0.002	0.998	0.000
Z61.4 Problems related to alleged sexual abuse of child by person within primary support group	0.002	0.998	0.000
Q90.2 Trisomy 21, translocation	0.002	0.998	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.002	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.002	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.002	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.002	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.002	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.002	0.998	0.000
Q96.0 Karyotype 45,X	0.002	0.998	0.000
S05.2 Ocular laceration and rupture with prolapse or loss of intraocular tissue	0.002	0.998	0.000
Q38.8 Other congenital malformations of pharynx	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
O81.4 Vacuum extractor delivery	0.000	0.998	0.002
Q21.9 Congenital malformation of cardiac septum, unspecified	0.002	0.998	0.000
Q99.9 Chromosomal abnormality, unspecified	0.002	0.998	0.000
Q99.2 Fragile X chromosome	0.002	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.002	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.002	0.998	0.000
A87 Viral meningitis	0.000	0.998	0.002
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
Q43.8 Other specified congenital malformations of intestine	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
Q44.4 Choledochal cyst	0.002	0.998	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.002	0.998	0.000
Q44.2 Atresia of bile ducts	0.002	0.998	0.000
Q44.1 Other congenital malformations of gallbladder	0.002	0.998	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.002	0.998	0.000
K74.3 Primary biliary cirrhosis	0.002	0.998	0.000
C53 Malignant neoplasm of cervix uteri	0.002	0.998	0.000
M21.19 Varus deformity, not elsewhere classified (Site unspecified)	0.002	0.998	0.000
M21.18 Varus deformity, not elsewhere classified (Other)	0.002	0.998	0.000
M21.15 Varus deformity, not elsewhere classified (Pelvic region and thigh)	0.002	0.998	0.000
M21.14 Varus deformity, not elsewhere classified (Hand)	0.002	0.998	0.000
M21.13 Varus deformity, not elsewhere classified (Forearm)	0.002	0.998	0.000
M21.12 Varus deformity, not elsewhere classified (Upper arm)	0.002	0.998	0.000
M21.11 Varus deformity, not elsewhere classified (Shoulder region)	0.002	0.998	0.000
M21.10 Varus deformity, not elsewhere classified (Multiple sites)	0.002	0.998	0.000
Q10.0 Congenital ptosis	0.002	0.998	0.000
M21 Other acquired deformities of limbs	0.002	0.998	0.000
Q15 Other congenital malformations of eye	0.002	0.998	0.000
M43.19 Spondylolisthesis (Site unspecified)	0.002	0.998	0.000
O81.5 Delivery by combination of forceps and vacuum extractor	0.000	0.998	0.002
O81.2 Mid-cavity forceps with rotation	0.000	0.998	0.002
O81.1 Mid-cavity forceps delivery	0.000	0.998	0.002
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
S05.7 Avulsion of eye	0.002	0.998	0.000
S05.5 Penetrating wound of eyeball with foreign body	0.002	0.998	0.000
S05.4 Penetrating wound of orbit with or without foreign body	0.002	0.998	0.000
J09-J18 Influenza and pneumonia	0.000	0.998	0.002
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
M80.19 Postoophorectomy osteoporosis with pathological fracture (Site unspecified)	0.002	0.998	0.000
M80.18 Postoophorectomy osteoporosis with pathological fracture (Other)	0.002	0.998	0.000
M80.17 Postoophorectomy osteoporosis with pathological fracture (Ankle and foot)	0.002	0.998	0.000
M80.16 Postoophorectomy osteoporosis with pathological fracture (Lower leg)	0.002	0.998	0.000
M80.15 Postoophorectomy osteoporosis with pathological fracture (Pelvic region and thigh)	0.002	0.998	0.000
M80.14 Postoophorectomy osteoporosis with pathological fracture (Hand)	0.002	0.998	0.000
M80.13 Postoophorectomy osteoporosis with pathological fracture (Forearm)	0.002	0.998	0.000
M80.12 Postoophorectomy osteoporosis with pathological fracture (Upper arm)	0.002	0.998	0.000
M80.11 Postoophorectomy osteoporosis with pathological fracture (Shoulder region)	0.002	0.998	0.000
M13.96 Arthritis, unspecified (Lower leg)	0.002	0.998	0.000
D03.9 Melanoma in situ, unspecified	0.000	0.998	0.002
D03.8 Melanoma in situ of other sites	0.000	0.998	0.002
D03.0 Melanoma in situ of lip	0.000	0.998	0.002
K74.4 Secondary biliary cirrhosis	0.002	0.998	0.000
K74.2 Hepatic fibrosis with hepatic sclerosis	0.002	0.998	0.000
K74.1 Hepatic sclerosis	0.002	0.998	0.000
S12 Fracture of neck	0.000	0.998	0.002
M21.2 Flexion deformity	0.002	0.998	0.000
Z61.9 Negative life events in childhood, unspecified	0.002	0.998	0.000
Z61.8 Other negative life events in childhood	0.002	0.998	0.000
Z61.7 Personal frightening experience in childhood	0.002	0.998	0.000
Z61.3 Events resulting in loss of self-esteem in childhood	0.002	0.998	0.000
Z61.2 Altered pattern of family relationships in childhood	0.002	0.998	0.000
Z61.1 Removal from home in childhood	0.002	0.998	0.000
Z61.0 Loss of love relationship in childhood	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
Q13 Congenital malformations of anterior segment of eye	0.002	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
Z61.5 Problems related to alleged sexual abuse of child by person outside primary support group	0.002	0.998	0.000
Q35 Cleft palate	0.002	0.998	0.000
I08.8 Other multiple valve diseases	0.002	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.002	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.002	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.002	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.002	0.998	0.000
Q98.5 Karyotype 47,XYY	0.002	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.002	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.002	0.998	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.002	0.998	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.002	0.998	0.000
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Z62 Other problems related to upbringing	0.002	0.998	0.000
Z55 Problems related to education and literacy	0.002	0.998	0.000
I08.9 Multiple valve disease, unspecified	0.002	0.998	0.000
Q23.0 Congenital stenosis of aortic valve	0.002	0.998	0.000
Q91.7 Patau's syndrome, unspecified	0.002	0.998	0.000
Q91.6 Trisomy 13, translocation	0.002	0.998	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.002	0.998	0.000
Q91.3 Edwards' syndrome, unspecified	0.002	0.998	0.000
Q91.2 Trisomy 18, translocation	0.002	0.998	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.002	0.998	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.002	0.998	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.002	0.998	0.000
Q92.7 Triploidy and polyploidy	0.002	0.998	0.000
Q92.6 Extra marker chromosomes	0.002	0.998	0.000
Q92.5 Duplications with other complex rearrangements	0.002	0.998	0.000
Q92.4 Duplications seen only at prometaphase	0.002	0.998	0.000
Q92.3 Minor partial trisomy	0.002	0.998	0.000
Q92.2 Major partial trisomy	0.002	0.998	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.002	0.998	0.000
Q93.9 Deletion from autosomes, unspecified	0.002	0.998	0.000
Q93.8 Other deletions from the autosomes	0.002	0.998	0.000
Q93.7 Deletions with other complex rearrangements	0.002	0.998	0.000
Q93.6 Deletions seen only at prometaphase	0.002	0.998	0.000
Q93.5 Other deletions of part of a chromosome	0.002	0.998	0.000
Q93.4 Deletion of short arm of chromosome 5	0.002	0.998	0.000
Q93.3 Deletion of short arm of chromosome 4	0.002	0.998	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.002	0.998	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.002	0.998	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.002	0.998	0.000
Q95.8 Other balanced rearrangements and structural markers	0.002	0.998	0.000
Q95.5 Individuals with autosomal fragile site	0.002	0.998	0.000
Q95.4 Individuals with marker heterochromatin	0.002	0.998	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.002	0.998	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.002	0.998	0.000
Q95.1 Chromosome inversion in normal individual	0.002	0.998	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.002	0.998	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.002	0.998	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.002	0.998	0.000
Q97.3 Female with 46,XY karyotype	0.002	0.998	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.002	0.998	0.000
Q97.1 Female with more than three X chromosomes	0.002	0.998	0.000
Q97.0 Karyotype 47,XXX	0.002	0.998	0.000
M07.36 Other psoriatic arthropathies (Lower leg)	0.000	0.998	0.002
M21.39 Wrist or foot drop (acquired)-Site unspec	0.002	0.998	0.000
M21.38 Wrist or foot drop (acquired)-Other	0.002	0.998	0.000
M21.36 Wrist or foot drop (acquired)-Lower leg	0.002	0.998	0.000
M21.35 Wrist or foot drop (acquired)-Pelvic/thigh	0.002	0.998	0.000
M21.34 Wrist or foot drop (acquired) (Hand)	0.002	0.998	0.000
M21.33 Wrist or foot drop (acquired) (Forearm)	0.002	0.998	0.000
M21.32 Wrist or foot drop (acquired)-Upper arm	0.002	0.998	0.000
M21.31 Wrist or foot drop (acquired)-Shldr region	0.002	0.998	0.000
M21.30 Wrist or foot drop (acquired) (Multiple sites)	0.002	0.998	0.000
M21.8 Other specified acquired deformities of limbs	0.002	0.998	0.000
O81.0 Low forceps delivery	0.000	0.998	0.002
M07.37 Other psoriatic arthropathies (Ankle and foot)	0.000	0.998	0.002
M21.26 Flexion deformity (Lower leg)	0.002	0.998	0.000
E21.3 Hyperparathyroidism, unspecified	0.002	0.998	0.000
G50.0 Trigeminal neuralgia	0.002	0.998	0.000
Q37 Cleft palate with cleft lip	0.002	0.998	0.000
Q36 Cleft lip	0.002	0.998	0.000
D03.6 Melanoma in situ of upper limb, including shoulder	0.000	0.998	0.002
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.002	0.998	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.002	0.998	0.000
Q14.3 Congenital malformation of choroid	0.002	0.998	0.000
Q14.2 Congenital malformation of optic disk	0.002	0.998	0.000
Q14.0 Congenital malformation of vitreous humour	0.002	0.998	0.000
Q21.8 Other congenital malformations of cardiac septa	0.002	0.998	0.000
Q21.4 Aortopulmonary septal defect	0.002	0.998	0.000
Q21.2 Atrioventricular septal defect	0.002	0.998	0.000
Z57.8 Occupational exposure to other risk-factors	0.002	0.998	0.000
Z56 Problems related to employment and unemployment	0.002	0.998	0.000
M21.22 Flexion deformity (Upper arm)	0.002	0.998	0.000
G96.0 Cerebrospinal fluid leak	0.000	0.998	0.002
M30.1 Polyarteritis with lung involvement [Churg-Strauss]	0.002	0.998	0.000
Q12 Congenital lens malformations	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
G45.4 Transient global amnesia	0.000	0.998	0.002
N03.9 Unspecified	0.000	0.998	0.002
O83.9 Assisted single delivery, unspecified	0.000	0.998	0.002
O83.8 Other specified assisted single delivery	0.000	0.998	0.002
O83.4 Destructive operation for delivery	0.000	0.998	0.002
O83.3 Delivery of viable foetus in abdominal pregnancy	0.000	0.998	0.002
O83.2 Other manipulation-assisted delivery	0.000	0.998	0.002
O83.1 Other assisted breech delivery	0.000	0.998	0.002
O83.0 Breech extraction	0.000	0.998	0.002
O84.9 Multiple delivery, unspecified	0.000	0.998	0.002
O84.8 Other multiple delivery	0.000	0.998	0.002
O84.2 Multiple delivery, all by Caesarean section	0.000	0.998	0.002
O84.1 Multiple delivery, all by forceps and vacuum extractor	0.000	0.998	0.002
O84.0 Multiple delivery, all spontaneous	0.000	0.998	0.002
Q61.9 Cystic kidney disease, unspecified	0.002	0.998	0.000

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

The full results table can be downloaded from this page.

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

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

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

Variant-specific associations