TreeWAS – Variant ID: rs13289122

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
I05.9 Mitral valve disease, unspecified	0.206	0.794	0.000
I05 Rheumatic mitral valve diseases	0.171	0.829	0.000
I05.0 Mitral stenosis	0.157	0.842	0.000
I05.1 Rheumatic mitral insufficiency	0.132	0.868	0.000
I05.8 Other mitral valve diseases	0.128	0.872	0.000
I05.2 Mitral stenosis with insufficiency	0.128	0.872	0.000
I05-I09 Chronic rheumatic heart diseases	0.030	0.970	0.000
I06 Rheumatic aortic valve diseases	0.025	0.975	0.000
M45.X9 Ankylosing spondylitis (Site unspecified)	0.000	0.976	0.024
I09 Other rheumatic heart diseases	0.022	0.977	0.000
I06.0 Rheumatic aortic stenosis	0.020	0.980	0.000
I06.9 Rheumatic aortic valve disease, unspecified	0.019	0.981	0.000
I06.1 Rheumatic aortic insufficiency	0.018	0.982	0.000
I06.8 Other rheumatic aortic valve diseases	0.018	0.982	0.000
I06.2 Rheumatic aortic stenosis with insufficiency	0.018	0.982	0.000
I07 Rheumatic tricuspid valve diseases	0.017	0.983	0.000
I09.9 Rheumatic heart disease, unspecified	0.017	0.983	0.000
H43.1 Vitreous haemorrhage	0.017	0.983	0.000
I09.8 Other specified rheumatic heart diseases	0.016	0.984	0.000
I09.2 Chronic rheumatic pericarditis	0.016	0.984	0.000
I09.1 Rheumatic diseases of endocardium, valve unspecified	0.016	0.984	0.000
I09.0 Rheumatic myocarditis	0.016	0.984	0.000
R73.9 Hyperglycaemia, unspecified	0.000	0.986	0.014
H43 Disorders of vitreous body	0.014	0.986	0.000
M45 Ankylosing spondylitis	0.000	0.987	0.013
K14.8 Other diseases of tongue	0.013	0.987	0.000
I07.9 Tricuspid valve disease, unspecified	0.012	0.987	0.000
I07.8 Other tricuspid valve diseases	0.012	0.987	0.000
I07.2 Tricuspid stenosis with insufficiency	0.012	0.987	0.000
I07.0 Tricuspid stenosis	0.012	0.987	0.000
H43.3 Other vitreous opacities	0.013	0.987	0.000
H43.9 Disorder of vitreous body, unspecified	0.011	0.989	0.000
M45.X2 Ankylosing spondylitis (Cervical region)	0.000	0.989	0.011
D23.7 Skin of lower limb, including hip	0.000	0.989	0.011
H43.0 Vitreous prolapse	0.011	0.989	0.000
H43.2 Crystalline deposits in vitreous body	0.010	0.989	0.000
M45.X0 Ankylosing spondylitis (Multiple sites in spine)	0.000	0.990	0.010
H43-H45 Disorders of vitreous body and globe	0.010	0.990	0.000
M45.X8 Ankylosing spondylitis (Sacral and sacrococcygeal region)	0.000	0.990	0.010
M45.X7 Ankylosing spondylitis (Lumbosacral region)	0.000	0.990	0.010
M45.X5 Ankylosing spondylitis (Thoracolumbar region)	0.000	0.990	0.010
M45.X4 Ankylosing spondylitis (Thoracic region)	0.000	0.990	0.010
M45.X3 Ankylosing spondylitis (Cervicothoracic region)	0.000	0.990	0.010
M45.X1 Ankylosing spondylitis (Occipito-atlanto-axial region)	0.000	0.990	0.010
T85.8 Other complications of internal prosthetic devices, implants and grafts, not elsewhere classified	0.000	0.990	0.010
H44 Disorders of globe	0.010	0.990	0.000
H44.4 Hypotony of eye	0.009	0.991	0.000
M45.X6 Ankylosing spondylitis (Lumbar region)	0.000	0.991	0.009
N83.2 Other and unspecified ovarian cysts	0.009	0.991	0.000
H44.8 Other disorders of globe	0.008	0.992	0.000
H44.7 Retained (old) intraocular foreign body, nonmagnetic	0.008	0.992	0.000
I07.1 Tricuspid insufficiency	0.008	0.992	0.000
H45 Disorders of vitreous body and globe in diseases classified elsewhere	0.007	0.993	0.000
H44.1 Other endophthalmitis	0.007	0.993	0.000
H44.5 Degenerated conditions of globe	0.007	0.993	0.000
H44.9 Disorder of globe, unspecified	0.007	0.993	0.000
H44.6 Retained (old) intraocular foreign body, magnetic	0.007	0.993	0.000
H44.3 Other degenerative disorders of globe	0.007	0.993	0.000
H44.0 Purulent endophthalmitis	0.007	0.993	0.000
H44.2 Degenerative myopia	0.006	0.993	0.000
F33.9 Recurrent depressive disorder, unspecified	0.000	0.994	0.006
R80 Isolated proteinuria	0.000	0.994	0.006
N32.9 Bladder disorder, unspecified	0.006	0.994	0.000
O68.0 Labour and delivery complicated by foetal heart rate anomaly	0.000	0.994	0.006
M25.37 Other instability of joint (Ankle and foot)	0.006	0.994	0.000
H45.0 Vitreous haemorrhage in diseases classified elsewhere	0.005	0.994	0.000
H45.8 Other disorders of vitreous body and globe in diseases classified elsewhere	0.005	0.994	0.000
H45.1 Endophthalmitis in diseases classified elsewhere	0.005	0.994	0.000
N83.1 Corpus luteum cyst	0.005	0.995	0.000
K91.3 Postoperative intestinal obstruction	0.005	0.995	0.000
R73 Elevated blood glucose level	0.000	0.995	0.004
K57.2 Diverticular disease of large intestine with perforation and abscess	0.000	0.996	0.004
R26.3 Immobility	0.000	0.996	0.004
N83 Noninflammatory disorders of ovary, Fallopian tube and broad ligament	0.004	0.996	0.000
I49.9 Cardiac arrhythmia, unspecified	0.000	0.996	0.004
N83.5 Torsion of ovary, ovarian pedicle and Fallopian tube	0.004	0.996	0.000
Q28 Other congenital malformations of circulatory system	0.004	0.996	0.000
Z71.1 Person with feared complaint in whom no diagnosis is made	0.000	0.996	0.004
Q28.2 Arteriovenous malformation of cerebral vessels	0.004	0.996	0.000
C34.3 Lower lobe, bronchus or lung	0.000	0.996	0.004
C18.4 Transverse colon	0.000	0.996	0.004
O16 Unspecified maternal hypertension	0.000	0.996	0.004
N83.6 Haematosalpinx	0.003	0.996	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
C16.0 Cardia	0.003	0.997	0.000
N83.7 Haematoma of broad ligament	0.003	0.997	0.000
N83.4 Prolapse and hernia of ovary and Fallopian tube	0.003	0.997	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.003	0.997	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.003	0.997	0.000
Q96.9 Turner's syndrome, unspecified	0.003	0.997	0.000
Z03.9 Observation for suspected disease or condition, unspecified	0.000	0.997	0.003
T84.4 Mechanical complication of other internal orthopaedic devices, imnplants and grafts	0.000	0.997	0.003
O04.4 Incomplete, without complication	0.003	0.997	0.000
Q28.3 Other malformations of cerebral vessels	0.003	0.997	0.000
N83.3 Acquired atrophy of ovary and Fallopian tube	0.003	0.997	0.000
Z90.2 Acquired absence of lung [part of]	0.000	0.997	0.003
Q96 Turner's syndrome	0.003	0.997	0.000
Q25 Congenital malformations of great arteries	0.003	0.997	0.000
Q24 Other congenital malformations of heart	0.003	0.997	0.000
Q23.0 Congenital stenosis of aortic valve	0.003	0.997	0.000
Z57.5 Occupational exposure to toxic agents in other industries	0.003	0.997	0.000
H36.0 Diabetic retinopathy	0.003	0.997	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.003	0.997	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.003	0.997	0.000
Q28.1 Other malformations of precerebral vessels	0.003	0.997	0.000
Q23 Congenital malformations of aortic and mitral valves	0.003	0.997	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.003	0.997	0.000
Q64 Other congenital malformations of urinary system	0.003	0.997	0.000
J47 Bronchiectasis	0.003	0.997	0.000
Q24.5 Malformation of coronary vessels	0.003	0.997	0.000
S01.8 Open wound of other parts of head	0.000	0.997	0.003
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.003	0.997	0.000
Q25.4 Other congenital malformations of aorta	0.003	0.997	0.000
Q26 Congenital malformations of great veins	0.003	0.997	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.003	0.997	0.000
M21.16 Varus deformity, not elsewhere classified (Lower leg)	0.000	0.997	0.003
F33.0 Recurrent depressive disorder, current episode mild	0.000	0.997	0.003
Q22 Congenital malformations of pulmonary and tricuspid valves	0.003	0.997	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.003	0.997	0.000
B98.0 Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters	0.000	0.997	0.003
Q43.8 Other specified congenital malformations of intestine	0.003	0.997	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.003	0.997	0.000
Q82.2 Mastocytosis	0.003	0.997	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.003	0.997	0.000
Y85.0 Sequelae of motor-vehicle accident	0.003	0.997	0.000
F33 Recurrent depressive disorder	0.000	0.997	0.003
R26.8 Other and unspecified abnormalities of gait and mobility	0.000	0.997	0.003
Q43 Other congenital malformations of intestine	0.003	0.997	0.000
Q66.8 Other congenital deformities of feet	0.003	0.997	0.000
Q60-Q64 Congenital malformations of the urinary system	0.003	0.997	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.003	0.997	0.000
R26 Abnormalities of gait and mobility	0.000	0.997	0.003
Q25.1 Coarctation of aorta	0.002	0.997	0.000
R26.0 Ataxic gait	0.000	0.997	0.003
S01.1 Open wound of eyelid and periocular area	0.000	0.997	0.003
Q25.3 Stenosis of aorta	0.002	0.997	0.000
Q64.4 Malformation of urachus	0.002	0.997	0.000
B01.9 Varicella without complications	0.000	0.997	0.003
Q30 Congenital malformations of nose	0.002	0.997	0.000
O14.9 Preeclampsia, unspecified	0.000	0.997	0.003
Q99.8 Other specified chromosome abnormalities	0.002	0.997	0.000
S01.2 Open wound of nose	0.000	0.997	0.003
Q96.8 Other variants of Turner's syndrome	0.002	0.997	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.002	0.997	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.002	0.997	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.002	0.997	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.002	0.997	0.000
Q96.0 Karyotype 45,X	0.002	0.997	0.000
Q25.6 Stenosis of pulmonary artery	0.002	0.997	0.000
Q24.4 Congenital subaortic stenosis	0.002	0.998	0.000
Q24.3 Pulmonary infundibular stenosis	0.002	0.998	0.000
Q24.2 Cor triatriatum	0.002	0.998	0.000
Q24.1 Levocardia	0.002	0.998	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.002	0.998	0.000
Q25.8 Other congenital malformations of great arteries	0.002	0.998	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.998	0.000
Q25.2 Atresia of aorta	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
S01.5 Open wound of lip and oral cavity	0.000	0.998	0.002
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
Q23.2 Congenital mitral stenosis	0.002	0.998	0.000
Q24.8 Other specified congenital malformations of heart	0.002	0.998	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.002	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.002	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.002	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.002	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.002	0.998	0.000
Q24.6 Congenital heart block	0.002	0.998	0.000
Q25.0 Patent ductus arteriosus	0.002	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.002	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.002	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.002	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.002	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.002	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.002	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.002	0.998	0.000
Q64.0 Epispadias	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q82 Other congenital malformations of skin	0.002	0.998	0.000
Q31 Congenital malformations of larynx	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
Q12.0 Congenital cataract	0.002	0.998	0.000
Q22.1 Congenital pulmonary valve stenosis	0.002	0.998	0.000
Q90 Down's syndrome	0.002	0.998	0.000
Q12 Congenital lens malformations	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
H02.0 Entropion and trichiasis of eyelid	0.000	0.998	0.002
Q21.9 Congenital malformation of cardiac septum, unspecified	0.002	0.998	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.002	0.998	0.000
Q26.8 Other congenital malformations of great veins	0.002	0.998	0.000
Q26.6 Portal vein-hepatic artery fistula	0.002	0.998	0.000
Q26.5 Anomalous portal venous connexion	0.002	0.998	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.002	0.998	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.002	0.998	0.000
Q26.1 Persistent left superior vena cava	0.002	0.998	0.000
Q26.0 Congenital stenosis of vena cava	0.002	0.998	0.000
Q30.3 Congenital perforated nasal septum	0.002	0.998	0.000
Q61 Cystic kidney disease	0.002	0.998	0.000
Q66 Congenital deformities of feet	0.002	0.998	0.000
R80-R82 Abnormal findings on examination of urine, without diagnosis	0.000	0.998	0.002
Q24.0 Dextrocardia	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
C49.2 Connective and soft tissue of lower limb, including hip	0.000	0.998	0.002
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.002	0.998	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.002	0.998	0.000
Q22.6 Hypoplastic right heart syndrome	0.002	0.998	0.000
Q22.4 Congenital tricuspid stenosis	0.002	0.998	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.002	0.998	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.002	0.998	0.000
Q22.0 Pulmonary valve atresia	0.002	0.998	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.002	0.998	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.002	0.998	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
Q20.6 Isomerism of atrial appendages	0.002	0.998	0.000
Q20.5 Discordant atrioventricular connexion	0.002	0.998	0.000
Q20.4 Double inlet ventricle	0.002	0.998	0.000
Q20.3 Discordant ventriculoarterial connexion	0.002	0.998	0.000
Q20.2 Double outlet left ventricle	0.002	0.998	0.000
Q20.1 Double outlet right ventricle	0.002	0.998	0.000
Q20.0 Common arterial trunk	0.002	0.998	0.000
Q30.9 Congenital malformation of nose, unspecified	0.002	0.998	0.000
Q61.9 Cystic kidney disease, unspecified	0.002	0.998	0.000
Q66.3 Other congenital varus deformities of feet	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
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.002	0.998	0.000
Q37 Cleft palate with cleft lip	0.002	0.998	0.000
N83.8 Other noninflammatory disorders of ovary, Fallopian tube and broad ligament	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
Q22.5 Ebstein's anomaly	0.002	0.998	0.000
Q38.1 Ankyloglossia	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
Q23.1 Congenital insufficiency of aortic valve	0.002	0.998	0.000
Q31.3 Laryngocele	0.002	0.998	0.000
F33.1 Recurrent depressive disorder, current episode moderate	0.000	0.998	0.002
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
Q43.7 Persistent cloaca	0.002	0.998	0.000
Q43.6 Congenital fistula of rectum and anus	0.002	0.998	0.000
Q43.5 Ectopic anus	0.002	0.998	0.000
Q43.4 Duplication of intestine	0.002	0.998	0.000
Q43.2 Other congenital functional disorders of colon	0.002	0.998	0.000
Q43.1 Hirschsprung's disease	0.002	0.998	0.000
Q85.9 Phakomatosis, unspecified	0.002	0.998	0.000
S01 Open wound of head	0.000	0.998	0.002
R26.1 Paralytic gait	0.000	0.998	0.002
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
Q61.2 Polycystic kidney, adult type	0.002	0.998	0.000
R41.8 Other and unspecified symptoms and signs involving cognitive functions and awareness	0.000	0.998	0.002
R78.0 Finding of alcohol in blood	0.000	0.998	0.002
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q30.8 Other congenital malformations of nose	0.002	0.998	0.000
Q30.2 Fissured, notched and cleft nose	0.002	0.998	0.000
Q30.1 Agenesis and underdevelopment of nose	0.002	0.998	0.000
Q30.0 Choanal atresia	0.002	0.998	0.000
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
F33.8 Other recurrent depressive disorders	0.000	0.998	0.002
Q23.3 Congenital mitral insufficiency	0.002	0.998	0.000
Q43.3 Congenital malformations of intestinal fixation	0.002	0.998	0.000
R77.1 Abnormality of globulin	0.000	0.998	0.002
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
Q44.6 Cystic disease of liver	0.002	0.998	0.000
Q66.6 Other congenital valgus deformities of feet	0.002	0.998	0.000
T78.2 Anaphylactic shock, unspecified	0.000	0.998	0.002
Q37.9 Unspecified cleft palate with unilateral cleft lip	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.002	0.998	0.000
Q36 Cleft lip	0.002	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.002	0.998	0.000
D36.1 Peripheral nerves and autonomic nervous system	0.000	0.998	0.002
Q38.5 Congenital malformations of palate, not elsewhere classified	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	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
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.002	0.998	0.000
Q84 Other congenital malformations of integument	0.002	0.998	0.000
Q81 Epidermolysis bullosa	0.002	0.998	0.000
Q80 Congenital ichthyosis	0.002	0.998	0.000
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
E05.9 Thyrotoxicosis, unspecified	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
Q82.8 Other specified congenital malformations of skin	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
Z92.3 Personal history of irradiation	0.002	0.998	0.000
R78 Findings of drugs and other substances, not normally found in blood	0.000	0.998	0.002
C49.9 Connective and soft tissue, unspecified	0.000	0.998	0.002
Q10.0 Congenital ptosis	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.998	0.000
Q35 Cleft palate	0.002	0.998	0.000
Q31.9 Congenital malformation of larynx, unspecified	0.002	0.998	0.000
Q31.8 Other congenital malformations of larynx	0.002	0.998	0.000
Q31.5 Congenital laryngomalacia	0.002	0.998	0.000
Q31.4 Congenital laryngeal stridor	0.002	0.998	0.000
Q31.2 Laryngeal hypoplasia	0.002	0.998	0.000
Q31.1 Congenital subglottic stenosis	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
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q82.9 Congenital malformation of skin, unspecified	0.002	0.998	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.002	0.998	0.000
Q82.3 Incontinentia pigmenti	0.002	0.998	0.000
Q82.1 Xeroderma pigmentosum	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
Q15 Other congenital malformations of eye	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
R77 Other abnormalities of plasma proteins	0.000	0.998	0.002
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
I79.2 Peripheral angiopathy in diseases classified elsewhere	0.000	0.998	0.002
Q12.9 Congenital lens malformation, unspecified	0.002	0.998	0.000
Q12.8 Other congenital lens malformations	0.002	0.998	0.000
Q12.4 Spherophakia	0.002	0.998	0.000
Q12.3 Congenital aphakia	0.002	0.998	0.000
Q12.2 Coloboma of lens	0.002	0.998	0.000
Q12.1 Congenital displaced lens	0.002	0.998	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.002	0.998	0.000
Q39.8 Other congenital malformations of oesophagus	0.002	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.002	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.002	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.002	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.002	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the 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
Q61.8 Other cystic kidney diseases	0.002	0.998	0.000
Q61.5 Medullary cystic kidney	0.002	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.002	0.998	0.000
Q66.5 Congenital pes planus	0.002	0.998	0.000
Q66.4 Talipes calcaneovalgus	0.002	0.998	0.000
Q66.1 Talipes calcaneovarus	0.002	0.998	0.000
C49 Malignant neoplasm of other connective and soft tissue	0.000	0.998	0.002
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q89 Other congenital malformations, not elsewhere classified	0.002	0.998	0.000
R70 Elevated erythrocyte sedimentation rate and abnormality of plasma viscosity	0.000	0.998	0.002
C49.0 Connective and soft tissue of head, face and neck	0.000	0.998	0.002
Q31.0 Web of larynx	0.002	0.998	0.000
Q38.8 Other congenital malformations of pharynx	0.002	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.002	0.998	0.000
Q44.4 Choledochal cyst	0.002	0.998	0.000
Z80.4 Family history of malignant neoplasm of genital organs	0.002	0.998	0.000
H26.1 Traumatic cataract	0.000	0.998	0.002
Q32.4 Other congenital malformations of bronchus	0.002	0.998	0.000
Q32.3 Congenital stenosis of bronchus	0.002	0.998	0.000
Q32.2 Congenital bronchomalacia	0.002	0.998	0.000
Q32.1 Other congenital malformations of trachea	0.002	0.998	0.000
Q32.0 Congenital tracheomalacia	0.002	0.998	0.000
Q33.9 Congenital malformation of lung, unspecified	0.002	0.998	0.000
Q33.8 Other congenital malformations of lung	0.002	0.998	0.000
Q33.6 Hypoplasia and dysplasia of lung	0.002	0.998	0.000
Q33.5 Ectopic tissue in lung	0.002	0.998	0.000
Q33.4 Congenital bronchiectasis	0.002	0.998	0.000
Q33.3 Agenesis of lung	0.002	0.998	0.000
Q33.2 Sequestration of lung	0.002	0.998	0.000
Q33.1 Accessory lobe of lung	0.002	0.998	0.000
Q33.0 Congenital cystic lung	0.002	0.998	0.000
Q34.9 Congenital malformation of respiratory system, unspecified	0.002	0.998	0.000
Q34.8 Other specified congenital malformations of respiratory system	0.002	0.998	0.000
Q34.1 Congenital cyst of mediastinum	0.002	0.998	0.000
Q34.0 Anomaly of pleura	0.002	0.998	0.000
Q90.9 Down's syndrome, unspecified	0.002	0.998	0.000
M25.55 Pain in joint (Pelvic region and thigh)	0.000	0.998	0.002
N85.0 Endometrial glandular hyperplasia	0.000	0.998	0.002
Q21.0 Ventricular septal defect	0.002	0.998	0.000
Q37.8 Unspecified cleft palate with bilateral cleft lip	0.002	0.998	0.000
Q37.5 Cleft hard and soft palate with unilateral cleft lip	0.002	0.998	0.000
Q37.4 Cleft hard and soft palate with bilateral cleft lip	0.002	0.998	0.000
Q37.3 Cleft soft palate with unilateral cleft lip	0.002	0.998	0.000
Q37.2 Cleft soft palate with bilateral cleft lip	0.002	0.998	0.000
Q37.1 Cleft hard palate with unilateral cleft lip	0.002	0.998	0.000
Q37.0 Cleft hard palate with bilateral cleft lip	0.002	0.998	0.000
R70.0 Elevated erythrocyte sedimentation rate	0.000	0.998	0.002
R77.9 Abnormality of plasma protein, unspecified	0.000	0.998	0.002
F33.2 Recurrent depressive disorder, current episode severe without psychotic symptoms	0.000	0.998	0.002
Q66.9 Congenital deformity of feet, unspecified	0.002	0.998	0.000
Q66.7 Pes cavus	0.002	0.998	0.000
Q66.0 Talipes equinovarus	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
Z11.2 Special screening examination for other bacterial diseases	0.002	0.998	0.000
O14 Gestational [pregnancy-induced] hypertension with significant proteinuria	0.000	0.998	0.002
Q14 Congenital malformations of posterior segment of eye	0.002	0.998	0.000
R81 Glycosuria	0.000	0.998	0.002
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
R70-R79 Abnormal findings on examination of blood, without diagnosis	0.000	0.998	0.002
F32.2 Severe depressive episode without psychotic symptoms	0.000	0.998	0.002
Q38.6 Other congenital malformations of mouth	0.002	0.998	0.000
F33.4 Recurrent depressive disorder, currently in remission	0.000	0.998	0.002
L50.9 Urticaria, unspecified	0.000	0.998	0.002
M18.0 Primary arthrosis of first carpometacarpal joints, bilateral	0.002	0.998	0.000
Q10.7 Congenital malformation of orbit	0.002	0.998	0.000
Q10.6 Other congenital malformations of lachrymal apparatus	0.002	0.998	0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct	0.002	0.998	0.000
Q10.4 Absence and agenesis of lachrymal apparatus	0.002	0.998	0.000
Q10.3 Other congenital malformations of eyelid	0.002	0.998	0.000
Q10.2 Congenital entropion	0.002	0.998	0.000
Q10.1 Congenital ectropion	0.002	0.998	0.000
R82.8 Abnormal findings on cytological and histological examination of urine	0.000	0.998	0.002
Q66.2 Metatarsus varus	0.002	0.998	0.000
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
M54.59 Low back pain (Site unspecified)	0.000	0.998	0.002
Q61.4 Renal dysplasia	0.002	0.998	0.000
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
Q78.0 Osteogenesis imperfecta	0.002	0.998	0.000
R77.0 Abnormality of albumin	0.000	0.998	0.002
R78.8 Finding of other specified substances, not normally found in blood	0.000	0.998	0.002
C18.8 Overlapping lesion of colon	0.000	0.998	0.002
C49.4 Connective and soft tissue of abdomen	0.000	0.998	0.002
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
Q82.0 Hereditary lymphoedema	0.002	0.998	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.002	0.998	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.002	0.998	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.002	0.998	0.000
R70.1 Abnormal plasma viscosity	0.000	0.998	0.002
Q63 Other congenital malformations of kidney	0.002	0.998	0.000
D13.2 Duodenum	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