TreeWAS – Variant ID: rs11834041

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
Z83.5 Family history of eye and ear disorders	0.000	0.973	0.027
R39.8 Other and unspecified symptoms and signs involving the urinary system	0.000	0.975	0.025
Z83 Family history of other specific disorders	0.000	0.984	0.016
Z83.7 Family history of diseases of the digestive system	0.000	0.986	0.014
Z83.4 Family history of other endocrine, nutritional and metabolic diseases	0.000	0.986	0.014
Z83.2 Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.000	0.987	0.013
Z83.1 Family history of other infectious and parasitic diseases	0.000	0.988	0.012
Z83.0 Family history of human immunodeficiency virus [HIV]	0.000	0.988	0.012
K81.0 Acute cholecystitis	0.011	0.989	0.000
Z83.6 Family history of diseases of the respiratory system	0.000	0.990	0.009
N20.0 Calculus of kidney	0.009	0.991	0.000
B95.4 Other streptococcus as the cause of diseases classified to other chapters	0.000	0.993	0.007
A41.5 Septicaemia due to other Gram-negative organisms	0.000	0.993	0.007
R39 Other symptoms and signs involving the urinary system	0.000	0.993	0.007
Z83.3 Family history of diabetes mellitus	0.000	0.994	0.006
R44.1 Visual hallucinations	0.006	0.994	0.000
E80.4 Gilbert's syndrome	0.006	0.994	0.000
R44 Other symptoms and signs involving general sensations and perceptions	0.005	0.995	0.000
R39.2 Extrarenal uraemia	0.000	0.995	0.005
R39.0 Extravasation of urine	0.000	0.995	0.005
R44.0 Auditory hallucinations	0.005	0.995	0.000
R44.3 Hallucinations, unspecified	0.005	0.995	0.000
H34.2 Other retinal artery occlusions	0.000	0.995	0.005
H34.8 Other retinal vascular occlusions	0.000	0.996	0.004
M47.92 Spondylosis, unspecified (Cervical region)	0.004	0.996	0.000
H34 Retinal vascular occlusions	0.000	0.996	0.004
C43.7 Malignant melanoma of lower limb, including hip	0.000	0.996	0.004
R44.2 Other hallucinations	0.004	0.996	0.000
M77.91 Enthesopathy, unspecified (Shoulder region)	0.004	0.996	0.000
R44.8 Other and unspecified symptoms and signs involving general sensations and perceptions	0.004	0.996	0.000
N95.8 Other specified menopausal and perimenopausal disorders	0.000	0.997	0.003
H34.1 Central retinal artery occlusion	0.000	0.997	0.003
R40.2 Coma, unspecified	0.000	0.997	0.003
I51.8 Other ill-defined heart diseases	0.003	0.997	0.000
I84.2 Internal haemorrhoids without complication	0.003	0.997	0.000
H34.9 Retinal vascular occlusion, unspecified	0.000	0.997	0.003
H34.0 Transient retinal artery occlusion	0.000	0.997	0.003
A41 Other septicaemia	0.000	0.997	0.003
C73 Malignant neoplasm of thyroid gland	0.003	0.997	0.000
A49.1 Streptococcal infection, unspecified	0.000	0.997	0.003
R39.1 Other difficulties with micturition	0.000	0.997	0.003
A41.2 Septicaemia due to unspecified staphylococcus	0.000	0.997	0.003
L43.9 Lichen planus, unspecified	0.000	0.997	0.003
B95 Streptococcus and staphylococcus as the cause of diseases classified to other chapters	0.000	0.997	0.003
A41.8 Other specified septicaemia	0.000	0.997	0.003
C43.6 Malignant melanoma of upper limb, including shoulder	0.000	0.997	0.003
C43 Malignant melanoma of skin	0.000	0.997	0.003
O03.4 Incomplete, without complication	0.003	0.997	0.000
M77.9 Enthesopathy, unspecified	0.003	0.997	0.000
B95.7 Other staphylococcus as the cause of diseases classified to other chapters	0.000	0.997	0.003
B95.3 Streptococcus pneumoniae as the cause of diseases classified to other chapters	0.000	0.997	0.003
A41.4 Septicaemia due to anaerobes	0.000	0.997	0.002
A41.3 Septicaemia due to Haemophilus influenzae	0.000	0.997	0.002
A41.0 Septicaemia due to Staphylococcus aureus	0.000	0.998	0.002
C43.5 Malignant melanoma of trunk	0.000	0.998	0.002
E80 Disorders of porphyrin and bilirubin metabolism	0.002	0.998	0.000
B95.5 Unspecified streptococcus as the cause of diseases classified to other chapters	0.000	0.998	0.002
Z89.6 Acquired absence of leg above knee	0.002	0.998	0.000
Q25 Congenital malformations of great arteries	0.002	0.998	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.002	0.998	0.000
M77.95 Enthesopathy, unspecified (Pelvic region and thigh)	0.002	0.998	0.000
Q25.3 Stenosis of aorta	0.002	0.998	0.000
M77.94 Enthesopathy, unspecified (Hand)	0.002	0.998	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.002	0.998	0.000
B95.0 Streptococcus, group A, as the cause of diseases classified to other chapters	0.000	0.998	0.002
Q23.0 Congenital stenosis of aortic valve	0.002	0.998	0.000
M77.96 Enthesopathy, unspecified (Lower leg)	0.002	0.998	0.000
C43.9 Malignant melanoma of skin, unspecified	0.000	0.998	0.002
C43.2 Malignant melanoma of ear and external auricular canal	0.000	0.998	0.002
Q23 Congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.002	0.998	0.000
A41.1 Septicaemia due to other specified staphylococcus	0.000	0.998	0.002
C43.8 Overlapping malignant melanoma of skin	0.000	0.998	0.002
C43.1 Malignant melanoma of eyelid, including canthus	0.000	0.998	0.002
C43.0 Malignant melanoma of lip	0.000	0.998	0.002
Q25.0 Patent ductus arteriosus	0.002	0.998	0.000
M77.99 Enthesopathy, unspecified (Site unspecified)	0.002	0.998	0.000
M77.98 Enthesopathy, unspecified (Other)	0.002	0.998	0.000
M77.93 Enthesopathy, unspecified (Forearm)	0.002	0.998	0.000
M77.92 Enthesopathy, unspecified (Upper arm)	0.002	0.998	0.000
M77.90 Enthesopathy, unspecified (Multiple sites)	0.002	0.998	0.000
B95.2 Streptococcus, group D, as the cause of diseases classified to other chapters	0.000	0.998	0.002
Q25.1 Coarctation of aorta	0.002	0.998	0.000
Q60-Q64 Congenital malformations of the urinary system	0.002	0.998	0.000
E16.2 Hypoglycaemia, unspecified	0.000	0.998	0.002
L43 Lichen planus	0.000	0.998	0.002
L40.9 Psoriasis, unspecified	0.000	0.998	0.002
C43.3 Malignant melanoma of other and unspecified parts of face	0.000	0.998	0.002
D22.6 Melanocytic naevi of upper limb, including shoulder	0.000	0.998	0.002
E80.7 Disorder of bilirubin metabolism, unspecified	0.002	0.998	0.000
E80.6 Other disorders of bilirubin metabolism	0.002	0.998	0.000
E80.5 Crigler-Najjar syndrome	0.002	0.998	0.000
E80.3 Defects of catalase and peroxydase	0.002	0.998	0.000
E80.2 Other porphyria	0.002	0.998	0.000
E80.1 Porphyria cutanea tarda	0.002	0.998	0.000
E80.0 Hereditary erythropoietic porphyria	0.002	0.998	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
J86.9 Pyothorax without fistula	0.000	0.998	0.002
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
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.998	0.000
Q25.6 Stenosis of pulmonary artery	0.002	0.998	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.998	0.000
Q25.4 Other congenital malformations of aorta	0.002	0.998	0.000
Q25.2 Atresia of aorta	0.002	0.998	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
M77.97 Enthesopathy, unspecified (Ankle and foot)	0.002	0.998	0.000
Q61.2 Polycystic kidney, adult type	0.002	0.998	0.000
A49 Bacterial infection of unspecified site	0.000	0.998	0.002
Q61 Cystic kidney disease	0.002	0.998	0.000
A49.8 Other bacterial infections of unspecified site	0.000	0.998	0.002
L27.0 Generalised skin eruption due to drugs and medicaments	0.000	0.998	0.002
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
I65.2 Occlusion and stenosis of carotid artery	0.000	0.998	0.002
Q24 Other congenital malformations of heart	0.002	0.998	0.000
L43.8 Other lichen planus	0.000	0.998	0.002
Q51.8 Other congenital malformations of uterus and cervix	0.002	0.998	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.002	0.998	0.000
Q63.2 Ectopic kidney	0.002	0.998	0.000
Z89.9 Acquired absence of limb, unspecified	0.002	0.998	0.000
L40.0 Psoriasis vulgaris	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
Q23.3 Congenital mitral insufficiency	0.002	0.998	0.000
Q23.2 Congenital mitral stenosis	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
Q61.5 Medullary cystic kidney	0.002	0.998	0.000
L40 Psoriasis	0.000	0.998	0.002
I84.6 Residual haemorrhoidal skin tags	0.002	0.998	0.000
Q63.0 Accessory kidney	0.002	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.002	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
L43.3 Subacute (active) lichen planus	0.000	0.998	0.002
L43.2 Lichenoid drug reaction	0.000	0.998	0.002
L43.1 Bullous lichen planus	0.000	0.998	0.002
L43.0 Hypertrophic lichen planus	0.000	0.998	0.002
Q21.1 Atrial septal defect	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q51.2 Other doubling of uterus	0.002	0.998	0.000
Q51 Congenital malformations of uterus and cervix	0.002	0.998	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.998	0.000
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
B95.1 Streptococcus, group B, as the cause of diseases classified to other chapters	0.000	0.998	0.002
K81 Cholecystitis	0.002	0.998	0.000
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q23.1 Congenital insufficiency of aortic valve	0.002	0.998	0.000
Q79.6 Ehlers-Danlos syndrome	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
R82.9 Other and unspecified abnormal finding in urine	0.000	0.998	0.002
Q66 Congenital deformities of feet	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	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
Q64 Other congenital malformations of urinary system	0.002	0.998	0.000
Q96 Turner's syndrome	0.002	0.998	0.000
B95.8 Unspecified staphylococcus as the cause of diseases classified to other chapters	0.000	0.998	0.002
Q21.9 Congenital malformation of cardiac septum, 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
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
Q21.2 Atrioventricular septal defect	0.002	0.998	0.000
R73.9 Hyperglycaemia, unspecified	0.000	0.998	0.002
Q38 Other congenital malformations of tongue, mouth and pharynx	0.002	0.998	0.000
A49.3 Mycoplasma infection, unspecified	0.000	0.998	0.002
Q61.8 Other cystic kidney diseases	0.002	0.998	0.000
Q61.4 Renal dysplasia	0.002	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.002	0.998	0.000
Q24.5 Malformation of coronary vessels	0.002	0.998	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.001	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.998	0.000
S42.20 Fracture of upper end of humerus (closed)	0.000	0.998	0.002
M95.0 Acquired deformity of nose	0.002	0.998	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.001	0.998	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.001	0.998	0.000
Q20.6 Isomerism of atrial appendages	0.001	0.998	0.000
Q20.5 Discordant atrioventricular connexion	0.001	0.998	0.000
Q20.4 Double inlet ventricle	0.001	0.998	0.000
Q20.3 Discordant ventriculoarterial connexion	0.001	0.998	0.000
Q20.2 Double outlet left ventricle	0.001	0.998	0.000
Q20.1 Double outlet right ventricle	0.001	0.998	0.000
Q20.0 Common arterial trunk	0.001	0.998	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.001	0.998	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.001	0.998	0.000
Q22.6 Hypoplastic right heart syndrome	0.001	0.998	0.000
Q22.5 Ebstein's anomaly	0.001	0.998	0.000
Q22.4 Congenital tricuspid stenosis	0.001	0.998	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.001	0.998	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.001	0.998	0.000
Q22.1 Congenital pulmonary valve stenosis	0.001	0.998	0.000
Q22.0 Pulmonary valve atresia	0.001	0.998	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.001	0.998	0.000
Q26.8 Other congenital malformations of great veins	0.001	0.998	0.000
Q26.6 Portal vein-hepatic artery fistula	0.001	0.998	0.000
Q26.5 Anomalous portal venous connexion	0.001	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.001	0.998	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.001	0.998	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.001	0.998	0.000
Q26.1 Persistent left superior vena cava	0.001	0.998	0.000
Q26.0 Congenital stenosis of vena cava	0.001	0.998	0.000
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.001	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.001	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.001	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.001	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.001	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.001	0.998	0.000
Q90 Down's syndrome	0.001	0.998	0.000
C75.1 Pituitary gland	0.002	0.998	0.000
Q61.9 Cystic kidney disease, unspecified	0.002	0.998	0.000
Q74.1 Congenital malformation of knee	0.001	0.998	0.000
Q12 Congenital lens malformations	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.001	0.998	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.001	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.001	0.998	0.000
Q73 Reduction defects of unspecified limb	0.001	0.998	0.000
Q72 Reduction defects of lower limb	0.001	0.998	0.000
Q71 Reduction defects of upper limb	0.001	0.998	0.000
Q70 Syndactyly	0.001	0.998	0.000
Q69 Polydactyly	0.001	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.001	0.998	0.000
O02.1 Missed abortion	0.002	0.998	0.000
Q21.0 Ventricular septal defect	0.002	0.998	0.000
Q24.6 Congenital heart block	0.001	0.998	0.000
Q24.4 Congenital subaortic stenosis	0.001	0.998	0.000
Q24.3 Pulmonary infundibular stenosis	0.001	0.998	0.000
Q24.2 Cor triatriatum	0.001	0.998	0.000
Q24.1 Levocardia	0.001	0.998	0.000
Q24.0 Dextrocardia	0.001	0.998	0.000
Q66.2 Metatarsus varus	0.001	0.998	0.000
R10.3 Pain localised to other parts of lower abdomen	0.000	0.998	0.002
Z01.5 Diagnostic skin and sensitisation tests	0.002	0.998	0.000
Z89.5 Acquired absence of leg at or below knee	0.002	0.998	0.000
Q52 Other congenital malformations of female genitalia	0.001	0.998	0.000
C75 Malignant neoplasm of other endocrine glands and related structures	0.002	0.998	0.000
C73-C75 Malignant neoplasms of thyroid and other endocrine glands	0.002	0.998	0.000
A49.2 Haemophilus influenzae infection, unspecified	0.000	0.998	0.001
Q24.8 Other specified congenital malformations of heart	0.001	0.998	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.001	0.998	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.001	0.998	0.000
Q28.3 Other malformations of cerebral vessels	0.001	0.998	0.000
Q28.1 Other malformations of precerebral vessels	0.001	0.998	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.001	0.998	0.000
Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle	0.001	0.998	0.000
Q05 Spina bifida	0.001	0.998	0.000
A30-A49 Other bacterial diseases	0.000	0.998	0.002
Q96.9 Turner's syndrome, unspecified	0.001	0.998	0.000
Q78 Other osteochondrodysplasias	0.001	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.001	0.998	0.000
Z89 Acquired absence of limb	0.002	0.998	0.000
K81.8 Other cholecystitis	0.001	0.998	0.000
L40.8 Other psoriasis	0.000	0.998	0.001
L40.4 Guttate psoriasis	0.000	0.998	0.001
L40.3 Pustulosis palmaris et plantaris	0.000	0.998	0.001
L40.2 Acrodermatitis continua	0.000	0.998	0.001
L40.1 Generalised pustular psoriasis	0.000	0.998	0.001
Q61.3 Polycystic kidney, unspecified	0.002	0.998	0.000
Q62.8 Other congenital malformations of ureter	0.001	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.001	0.998	0.000
Q62.6 Malposition of ureter	0.001	0.998	0.000
Q62.5 Duplication of ureter	0.001	0.998	0.000
Q62.4 Agenesis of ureter	0.001	0.998	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.001	0.998	0.000
Q62.2 Congenital megaloureter	0.001	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.001	0.998	0.000
Q62.0 Congenital hydronephrosis	0.001	0.998	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.001	0.998	0.000
Q79.8 Other congenital malformations of musculoskeletal system	0.001	0.998	0.000
Q79.5 Other congenital malformations of abdominal wall	0.001	0.998	0.000
Q79.4 Prune belly syndrome	0.001	0.998	0.000
Q79.3 Gastroschisis	0.001	0.998	0.000
Q79.2 Exomphalos	0.001	0.998	0.000
Q79.1 Other congenital malformations of diaphragm	0.001	0.998	0.000
Q79.0 Congenital diaphragmatic hernia	0.001	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.001	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.001	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.001	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.001	0.998	0.000
Q98.5 Karyotype 47,XYY	0.001	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.001	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.001	0.998	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.001	0.998	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.001	0.998	0.000
Z89.7 Acquired absence of both lower limbs [any level, except toes alone]	0.001	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.001	0.998	0.000
Q15 Other congenital malformations of eye	0.001	0.998	0.000
Q14 Congenital malformations of posterior segment of eye	0.001	0.998	0.000
Q13 Congenital malformations of anterior segment of eye	0.001	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.001	0.998	0.000
Q65 Congenital deformities of hip	0.001	0.998	0.000
L72.8 Other follicular cysts of skin and subcutaneous tissue	0.002	0.998	0.000
N13.3 Other and unspecified hydronephrosis	0.002	0.998	0.000
Q17.5 Prominent ear	0.001	0.998	0.000
Q51.9 Congenital malformation of uterus and cervix, unspecified	0.001	0.998	0.000
Q51.7 Congenital fistulae between uterus and digestive and urinary tracts	0.001	0.998	0.000
Q51.6 Embryonic cyst of cervix	0.001	0.998	0.000
Q51.5 Agenesis and aplasia of cervix	0.001	0.998	0.000
Q51.4 Unicornate uterus	0.001	0.998	0.000
Q51.1 Doubling of uterus with doubling of cervix and vagina	0.001	0.998	0.000
Q51.0 Agenesis and aplasia of uterus	0.001	0.998	0.000
Q74.9 Unspecified congenital malformation of limb(s)	0.001	0.998	0.000
Q74.8 Other specified congenital malformations of limb(s)	0.001	0.998	0.000
Q74.3 Arthrogryposis multiplex congenita	0.001	0.998	0.000
Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle	0.001	0.998	0.000
Q45 Other congenital malformations of digestive system	0.001	0.998	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.001	0.998	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.001	0.998	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.001	0.998	0.000
Q55 Other congenital malformations of male genital organs	0.001	0.998	0.000
A49.9 Bacterial infection, unspecified	0.000	0.998	0.001
C43.4 Malignant melanoma of scalp and neck	0.000	0.998	0.001
Q24.9 Congenital malformation of the heart, unspecified	0.001	0.998	0.000
Q27.4 Congenital phlebectasia	0.001	0.998	0.000
Q27.2 Other congenital malformations of renal artery	0.001	0.998	0.000
Q27.1 Congenital renal artery stenosis	0.001	0.998	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.001	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.001	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.001	0.998	0.000
Q40.1 Congenital hiatus hernia	0.001	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.001	0.998	0.000
Q52.5 Fusion of labia	0.001	0.998	0.000
Q53 Undescended testicle	0.001	0.998	0.000
E88.0 Disorders of plasma-protein metabolism, not elsewhere classified	0.000	0.998	0.002
Q10.0 Congenital ptosis	0.001	0.998	0.000
Q12.0 Congenital cataract	0.001	0.998	0.000
Q66.9 Congenital deformity of feet, unspecified	0.001	0.998	0.000
Q66.7 Pes cavus	0.001	0.998	0.000
Q66.6 Other congenital valgus deformities of feet	0.001	0.998	0.000
Q66.5 Congenital pes planus	0.001	0.998	0.000
Q66.4 Talipes calcaneovalgus	0.001	0.998	0.000
Q66.3 Other congenital varus deformities of feet	0.001	0.998	0.000
Q66.1 Talipes calcaneovarus	0.001	0.998	0.000
Q66.0 Talipes equinovarus	0.001	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.001	0.998	0.000
Q04 Other congenital malformations of brain	0.001	0.998	0.000
Q03 Congenital hydrocephalus	0.001	0.998	0.000
Q01 Encephalocele	0.001	0.998	0.000
Q00 Anencephaly and similar malformations	0.001	0.998	0.000
Q02 Microcephaly	0.001	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.001	0.998	0.000
Q33 Congenital malformations of lung	0.001	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.001	0.998	0.000
Q31 Congenital malformations of larynx	0.001	0.998	0.000
Q30 Congenital malformations of nose	0.001	0.998	0.000
Q37 Cleft palate with cleft lip	0.001	0.998	0.000
Q36 Cleft lip	0.001	0.998	0.000
Q35 Cleft palate	0.001	0.998	0.000
Q76 Congenital malformations of spine and bony thorax	0.001	0.998	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.001	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.001	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.001	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.001	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.001	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.001	0.998	0.000
Q64.4 Malformation of urachus	0.001	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.001	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.001	0.998	0.000
Q64.0 Epispadias	0.001	0.998	0.000
Q66.8 Other congenital deformities of feet	0.001	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.001	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.001	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.001	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.001	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.001	0.998	0.000
Q96.0 Karyotype 45,X	0.001	0.998	0.000
T84.6 Infection and inflammatory reaction due to internal fixation device [any site]	0.002	0.998	0.000
Q28.2 Arteriovenous malformation of cerebral vessels	0.001	0.998	0.000
Q38.8 Other congenital malformations of pharynx	0.001	0.998	0.000
Q38.6 Other congenital malformations of mouth	0.001	0.998	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.001	0.998	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.001	0.998	0.000
Q38.3 Other congenital malformations of tongue	0.001	0.998	0.000
Q38.2 Macroglossia	0.001	0.998	0.000
Q38.1 Ankyloglossia	0.001	0.998	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.001	0.998	0.000
Q54.1 Hypospadias, penile	0.001	0.998	0.000
Z97.4 Presence of external hearing-aid	0.001	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.001	0.998	0.000
D59.1 Other autoimmune haemolytic anaemias	0.000	0.999	0.001
K63.9 Disease of intestine, unspecified	0.001	0.999	0.000
O00.1 Tubal pregnancy	0.001	0.999	0.000
Q05.9 Spina bifida, unspecified	0.001	0.999	0.000
Q60.6 Potter's syndrome	0.001	0.999	0.000
Q60.5 Renal hypoplasia, unspecified	0.001	0.999	0.000
Q60.4 Renal hypoplasia, bilateral	0.001	0.999	0.000
Q60.3 Renal hypoplasia, unilateral	0.001	0.999	0.000
Q60.1 Renal agenesis, bilateral	0.001	0.999	0.000
Q54 Hypospadias	0.001	0.999	0.000
L40-L45 Papulosquamous disorders	0.000	0.999	0.001
L89.9 Decubitus ulcer and pressure area, unspecified	0.001	0.999	0.000
Q17.9 Congenital malformation of ear, unspecified	0.001	0.999	0.000
Q17.8 Other specified congenital malformations of ear	0.001	0.999	0.000
Q17.4 Misplaced ear	0.001	0.999	0.000
Q17.3 Other misshapen ear	0.001	0.999	0.000
Q17.2 Microtia	0.001	0.999	0.000
Q17.1 Macrotia	0.001	0.999	0.000
Q17.0 Accessory auricle	0.001	0.999	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.001	0.999	0.000
Q68.5 Congenital bowing of long bones of leg, unspecified	0.001	0.999	0.000
Q68.4 Congenital bowing of tibia and fibula	0.001	0.999	0.000
Q68.3 Congenital bowing of femur	0.001	0.999	0.000
Q68.2 Congenital deformity of knee	0.001	0.999	0.000
Q68.1 Congenital deformity of hand	0.001	0.999	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.001	0.999	0.000
Q69.9 Polydactyly, unspecified	0.001	0.999	0.000
Q69.2 Accessory toe(s)	0.001	0.999	0.000
Q69.1 Accessory thumb(s)	0.001	0.999	0.000
Q69.0 Accessory finger(s)	0.001	0.999	0.000
Q70.9 Syndactyly, unspecified	0.001	0.999	0.000
Q70.4 Polysyndactyly	0.001	0.999	0.000
Q70.3 Webbed toes	0.001	0.999	0.000
Q70.2 Fused toes	0.001	0.999	0.000
Q70.1 Webbed fingers	0.001	0.999	0.000
Q70.0 Fused fingers	0.001	0.999	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.001	0.999	0.000
Q71.8 Other reduction defects of upper limb(s)	0.001	0.999	0.000
Q71.6 Lobster-claw hand	0.001	0.999	0.000
Q71.5 Longitudinal reduction defect of ulna	0.001	0.999	0.000
Q71.4 Longitudinal reduction defect of radius	0.001	0.999	0.000
Q71.3 Congenital absence of hand and finger(s)	0.001	0.999	0.000
Q71.2 Congenital absence of both forearm and hand	0.001	0.999	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.001	0.999	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.001	0.999	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.001	0.999	0.000
Q72.8 Other reduction defects of lower limb(s)	0.001	0.999	0.000
Q72.7 Split foot	0.001	0.999	0.000
Q72.6 Longitudinal reduction defect of fibula	0.001	0.999	0.000
Q72.5 Longitudinal reduction defect of tibia	0.001	0.999	0.000
Q72.4 Longitudinal reduction defect of femur	0.001	0.999	0.000
Q72.3 Congenital absence of foot and toe(s)	0.001	0.999	0.000
Q72.2 Congenital absence of both lower leg and foot	0.001	0.999	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.001	0.999	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.001	0.999	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.001	0.999	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.001	0.999	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.001	0.999	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.001	0.999	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.001	0.999	0.000
Q75.5 Oculomandibular dysostosis	0.001	0.999	0.000
Q75.4 Mandibulofacial dysostosis	0.001	0.999	0.000
Q75.3 Macrocephaly	0.001	0.999	0.000
Q75.2 Hypertelorism	0.001	0.999	0.000
Q75.1 Craniofacial dysostosis	0.001	0.999	0.000
Q75.0 Craniosynostosis	0.001	0.999	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.001	0.999	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.001	0.999	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.001	0.999	0.000
Q77.6 Chondroectodermal dysplasia	0.001	0.999	0.000
Q77.5 Diastrophic dysplasia	0.001	0.999	0.000
Q77.4 Achondroplasia	0.001	0.999	0.000
Q77.3 Chondrodysplasia punctata	0.001	0.999	0.000
Q77.2 Short rib syndrome	0.001	0.999	0.000
Q77.1 Thanatophoric short stature	0.001	0.999	0.000
Q77.0 Achondrogenesis	0.001	0.999	0.000
Q90.9 Down's syndrome, unspecified	0.001	0.999	0.000
Q90.2 Trisomy 21, translocation	0.001	0.999	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.001	0.999	0.000
Q91.7 Patau's syndrome, unspecified	0.001	0.999	0.000
Q91.6 Trisomy 13, translocation	0.001	0.999	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.001	0.999	0.000
Q91.3 Edwards' syndrome, unspecified	0.001	0.999	0.000
Q91.2 Trisomy 18, translocation	0.001	0.999	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.001	0.999	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.001	0.999	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.001	0.999	0.000
Q92.7 Triploidy and polyploidy	0.001	0.999	0.000
Q92.6 Extra marker chromosomes	0.001	0.999	0.000
Q92.5 Duplications with other complex rearrangements	0.001	0.999	0.000
Q92.4 Duplications seen only at prometaphase	0.001	0.999	0.000
Q92.3 Minor partial trisomy	0.001	0.999	0.000
Q92.2 Major partial trisomy	0.001	0.999	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.001	0.999	0.000
Q93.9 Deletion from autosomes, unspecified	0.001	0.999	0.000
Q93.8 Other deletions from the autosomes	0.001	0.999	0.000
Q93.7 Deletions with other complex rearrangements	0.001	0.999	0.000
Q93.6 Deletions seen only at prometaphase	0.001	0.999	0.000
Q93.5 Other deletions of part of a chromosome	0.001	0.999	0.000
Q93.4 Deletion of short arm of chromosome 5	0.001	0.999	0.000
Q93.3 Deletion of short arm of chromosome 4	0.001	0.999	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.001	0.999	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.001	0.999	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.001	0.999	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.001	0.999	0.000
Q95.8 Other balanced rearrangements and structural markers	0.001	0.999	0.000

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

The full results table can be downloaded from this page.

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

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

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

Variant-specific associations