TreeWAS – Variant ID: rs10067427

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
N87 Dysplasia of cervix uteri	0.000	0.072	0.928
N87.0 Mild cervical dysplasia	0.000	0.072	0.928
N87.9 Dysplasia of cervix uteri, unspecified	0.000	0.077	0.923
N87.1 Moderate cervical dysplasia	0.000	0.106	0.894
N87.2 Severe cervical dysplasia, not elsewhere classified	0.000	0.213	0.787
N85.2 Hypertrophy of uterus	0.133	0.867	0.000
I65.2 Occlusion and stenosis of carotid artery	0.047	0.953	0.000
M54.99 Dorsalgia, unspecified (Site unspecified)	0.045	0.955	0.000
M54.9 Dorsalgia, unspecified	0.034	0.966	0.000
M54.94 Dorsalgia, unspecified (Thoracic region)	0.028	0.972	0.000
M54.92 Dorsalgia, unspecified (Cervical region)	0.027	0.972	0.000
M54.96 Dorsalgia, unspecified (Lumbar region)	0.027	0.973	0.000
M54.98 Dorsalgia, unspecified (Sacral and sacrococcygeal region)	0.027	0.973	0.000
I65 Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction	0.026	0.974	0.000
M54.90 Dorsalgia, unspecified (Multiple sites in spine)	0.025	0.975	0.000
M54.95 Dorsalgia, unspecified (Thoracolumbar region)	0.024	0.975	0.000
M54.93 Dorsalgia, unspecified (Cervicothoracic region)	0.024	0.975	0.000
M54.91 Dorsalgia, unspecified (Occipito-atlanto-axial region)	0.024	0.975	0.000
M54.97 Dorsalgia, unspecified (Lumbosacral region)	0.024	0.976	0.000
I65.3 Occlusion and stenosis of multiple and bilateral precerebral arteries	0.021	0.979	0.000
I65.0 Occlusion and stenosis of vertebral artery	0.019	0.980	0.000
I65.9 Occlusion and stenosis of unspecified precerebral artery	0.019	0.981	0.000
I65.8 Occlusion and stenosis of other precerebral artery	0.019	0.981	0.000
I65.1 Occlusion and stenosis of basilar artery	0.018	0.982	0.000
I22.9 Subsequent myocardial infarction of unspecified site	0.000	0.989	0.011
I05.0 Mitral stenosis	0.011	0.989	0.000
I22 Subsequent myocardial infarction	0.000	0.990	0.010
I22.8 Subsequent myocardial infarction of other sites	0.000	0.991	0.009
S83.5 Sprain and strain involving (anterior)(posterior) cruciate ligament of knee	0.009	0.991	0.000
Z95.9 Presence of cardiac and vascular implant and graft, unspecified	0.009	0.991	0.000
I61.1 Intracerebral haemorrhage in hemisphere, cortical	0.009	0.991	0.000
I22.0 Subsequent myocardial infarction of anterior wall	0.000	0.991	0.009
I05.2 Mitral stenosis with insufficiency	0.009	0.991	0.000
I05 Rheumatic mitral valve diseases	0.008	0.991	0.000
J18.0 Bronchopneumonia, unspecified	0.008	0.992	0.000
I22.1 Subsequent myocardial infarction of inferior wall	0.000	0.993	0.007
I61 Intracerebral haemorrhage	0.007	0.993	0.000
I61.0 Intracerebral haemorrhage in hemisphere, subcortical	0.007	0.993	0.000
I05.8 Other mitral valve diseases	0.006	0.994	0.000
K70.3 Alcoholic cirrhosis of liver	0.006	0.994	0.000
Q66 Congenital deformities of feet	0.006	0.994	0.000
I05-I09 Chronic rheumatic heart diseases	0.006	0.994	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.006	0.994	0.000
I05.1 Rheumatic mitral insufficiency	0.006	0.994	0.000
Q66.8 Other congenital deformities of feet	0.006	0.994	0.000
K31.5 Obstruction of duodenum	0.006	0.994	0.000
I61.5 Intracerebral haemorrhage, intraventricular	0.005	0.994	0.000
I61.4 Intracerebral haemorrhage in cerebellum	0.005	0.994	0.000
D34 Benign neoplasm of thyroid gland	0.006	0.994	0.000
I61.2 Intracerebral haemorrhage in hemisphere, unspecified	0.005	0.995	0.000
Q66.7 Pes cavus	0.005	0.995	0.000
I61.3 Intracerebral haemorrhage in brain stem	0.005	0.995	0.000
K70.9 Alcoholic liver disease, unspecified	0.005	0.995	0.000
Q66.9 Congenital deformity of feet, unspecified	0.005	0.995	0.000
K31.9 Disease of stomach and duodenum, unspecified	0.005	0.995	0.000
I08 Multiple valve diseases	0.005	0.995	0.000
I60-I69 Cerebrovascular diseases	0.005	0.995	0.000
K31 Other diseases of stomach and duodenum	0.005	0.995	0.000
G83.4 Cauda equina syndrome	0.005	0.995	0.000
K70 Alcoholic liver disease	0.005	0.995	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.005	0.995	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.005	0.995	0.000
S83 Dislocation, sprain and strain of joints and ligaments of knee	0.005	0.995	0.000
I06 Rheumatic aortic valve diseases	0.005	0.995	0.000
Q76 Congenital malformations of spine and bony thorax	0.005	0.995	0.000
I09 Other rheumatic heart diseases	0.005	0.995	0.000
Q66.6 Other congenital valgus deformities of feet	0.005	0.995	0.000
Q85 Phakomatoses, not elsewhere classified	0.005	0.995	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.005	0.995	0.000
I61.6 Intracerebral haemorrhage, multiple localised	0.004	0.995	0.000
Q80-Q89 Other congenital malformations	0.005	0.995	0.000
K31.1 Adult hypertrophic pyloric stenosis	0.005	0.995	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.005	0.995	0.000
I61.8 Other intracerebral haemorrhage	0.005	0.995	0.000
Q38.1 Ankyloglossia	0.005	0.995	0.000
K31.8 Other specified diseases of stomach and duodenum	0.005	0.995	0.000
M19.07 Primary arthrosis of other joints (Ankle and foot)	0.000	0.995	0.005
Q66.5 Congenital pes planus	0.004	0.995	0.000
Q66.4 Talipes calcaneovalgus	0.004	0.995	0.000
Q66.3 Other congenital varus deformities of feet	0.004	0.995	0.000
Q66.1 Talipes calcaneovarus	0.004	0.995	0.000
Q78 Other osteochondrodysplasias	0.004	0.995	0.000
Q66.2 Metatarsus varus	0.004	0.995	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.005	0.995	0.000
I64 Stroke, not specified as haemorrhage or infarction	0.005	0.995	0.000
I08.2 Disorders of both aortic and tricuspid valves	0.004	0.996	0.000
Q38.7 Pharyngeal pouch	0.004	0.996	0.000
K31.0 Acute dilatation of stomach	0.004	0.996	0.000
K70.4 Alcoholic hepatic failure	0.004	0.996	0.000
S83.4 Sprain and strain involving (fibular)(tibial) collateral ligamnent of knee	0.004	0.996	0.000
Q83 Congenital malformations of breast	0.004	0.996	0.000
I08.9 Multiple valve disease, unspecified	0.004	0.996	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.004	0.996	0.000
K31.2 Hourglass stricture and stenosis of stomach	0.004	0.996	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.004	0.996	0.000
Q75 Other congenital malformations of skull and face bones	0.004	0.996	0.000
Q73 Reduction defects of unspecified limb	0.004	0.996	0.000
Q72 Reduction defects of lower limb	0.004	0.996	0.000
Q71 Reduction defects of upper limb	0.004	0.996	0.000
Q70 Syndactyly	0.004	0.996	0.000
Q69 Polydactyly	0.004	0.996	0.000
Q68 Other congenital musculoskeletal deformities	0.004	0.996	0.000
Q65 Congenital deformities of hip	0.004	0.996	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.004	0.996	0.000
I08.0 Disorders of both mitral and aortic valves	0.004	0.996	0.000
Q83.1 Accessory breast	0.004	0.996	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.004	0.996	0.000
K31.4 Gastric diverticulum	0.004	0.996	0.000
I08.1 Disorders of both mitral and tricuspid valves	0.004	0.996	0.000
Q76.0 Spina bifida occulta	0.004	0.996	0.000
Q79.6 Ehlers-Danlos syndrome	0.004	0.996	0.000
Q66.0 Talipes equinovarus	0.004	0.996	0.000
Q85.0 Neurofibromatosis (nonmalignant)	0.004	0.996	0.000
Q76.5 Cervical rib	0.004	0.996	0.000
I07 Rheumatic tricuspid valve diseases	0.004	0.996	0.000
I06.1 Rheumatic aortic insufficiency	0.004	0.996	0.000
Q38.8 Other congenital malformations of pharynx	0.004	0.996	0.000
I06.9 Rheumatic aortic valve disease, unspecified	0.004	0.996	0.000
I09.9 Rheumatic heart disease, unspecified	0.004	0.996	0.000
I66 Occlusion and stenosis of cerebral arteries, not resulting in cerebral infarction	0.004	0.996	0.000
Q43 Other congenital malformations of intestine	0.004	0.996	0.000
Q85.9 Phakomatosis, unspecified	0.004	0.996	0.000
Q79.8 Other congenital malformations of musculoskeletal system	0.004	0.996	0.000
R87.6 Abnormal cytological findings	0.000	0.996	0.004
Q90 Down's syndrome	0.004	0.996	0.000
Q00-Q07 Congenital malformations of the nervous system	0.004	0.996	0.000
Q78.2 Osteopetrosis	0.004	0.996	0.000
K75.9 Inflammatory liver disease, unspecified	0.004	0.996	0.000
S83.2 Tear of meniscus, current	0.004	0.996	0.000
Q35-Q37 Cleft lip and cleft palate	0.004	0.996	0.000
K31.3 Pylorospasm, not elsewhere classified	0.004	0.996	0.000
I08.8 Other multiple valve diseases	0.004	0.996	0.000
Q76.1 Klippel-Feil syndrome	0.004	0.996	0.000
I05.9 Mitral valve disease, unspecified	0.004	0.996	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.004	0.996	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.004	0.996	0.000
Q38.3 Other congenital malformations of tongue	0.004	0.996	0.000
Q38.2 Macroglossia	0.004	0.996	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.004	0.996	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.004	0.996	0.000
Q79.5 Other congenital malformations of abdominal wall	0.004	0.996	0.000
Q79.4 Prune belly syndrome	0.004	0.996	0.000
Q79.3 Gastroschisis	0.004	0.996	0.000
Q79.2 Exomphalos	0.004	0.996	0.000
Q79.1 Other congenital malformations of diaphragm	0.004	0.996	0.000
Q79.0 Congenital diaphragmatic hernia	0.004	0.996	0.000
Q90.9 Down's syndrome, unspecified	0.004	0.996	0.000
S83.1 Dislocation of knee	0.004	0.996	0.000
S83.0 Dislocation of patella	0.004	0.996	0.000
I06.8 Other rheumatic aortic valve diseases	0.004	0.996	0.000
I06.2 Rheumatic aortic stenosis with insufficiency	0.004	0.996	0.000
K70.0 Alcoholic fatty liver	0.004	0.996	0.000
Q83.3 Accessory nipple	0.004	0.996	0.000
Q38.6 Other congenital malformations of mouth	0.004	0.996	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.004	0.996	0.000
I68 Cerebrovascular disorders in diseases classified elsewhere	0.004	0.996	0.000
I09.8 Other specified rheumatic heart diseases	0.003	0.996	0.000
I09.2 Chronic rheumatic pericarditis	0.003	0.996	0.000
I09.1 Rheumatic diseases of endocardium, valve unspecified	0.003	0.996	0.000
I09.0 Rheumatic myocarditis	0.003	0.996	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.004	0.996	0.000
Q76.8 Other congenital malformations of bony thorax	0.004	0.996	0.000
Q76.7 Congenital malformation of sternum	0.004	0.996	0.000
Q76.6 Other congenital malformations of ribs	0.004	0.996	0.000
Q76.3 Congenital scoliosis due to congenital bony malformation	0.004	0.996	0.000
Q76.2 Congenital spondylolisthesis	0.004	0.996	0.000
Q43.0 Meckel's diverticulum	0.004	0.996	0.000
M86.97 Osteomyelitis, unspecified (Ankle and foot)	0.004	0.996	0.000
I06.0 Rheumatic aortic stenosis	0.003	0.996	0.000
K70.2 Alcoholic fibrosis and sclerosis of liver	0.004	0.996	0.000
Q85.1 Tuberous sclerosis	0.003	0.996	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.004	0.996	0.000
D52.9 Folate deficiency anaemia, unspecified	0.004	0.996	0.000
K92.9 Disease of digestive system, unspecified	0.004	0.996	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.003	0.996	0.000
Q84 Other congenital malformations of integument	0.003	0.996	0.000
Q81 Epidermolysis bullosa	0.003	0.996	0.000
Q80 Congenital ichthyosis	0.003	0.996	0.000
I66.3 Occlusion and stenosis of cerebellar arteries	0.003	0.996	0.000
N02.8 Other	0.004	0.996	0.000
Q67.8 Other congenital deformities of chest	0.003	0.996	0.000
Q67.7 Pectus carinatum	0.003	0.996	0.000
Q67.3 Plagiocephaly	0.003	0.996	0.000
Q67.2 Dolichocephaly	0.003	0.996	0.000
Q67.1 Compression facies	0.003	0.996	0.000
Q67.0 Facial asymmetry	0.003	0.996	0.000
Q96 Turner's syndrome	0.003	0.996	0.000
I61.9 Intracerebral haemorrhage, unspecified	0.004	0.996	0.000
Q74 Other congenital malformations of limb(s)	0.003	0.996	0.000
I63.5 Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries	0.004	0.996	0.000
K31.6 Fistula of stomach and duodenum	0.003	0.996	0.000
S83.7 Injury to multiple structures of knee	0.003	0.996	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.003	0.996	0.000
Q43.8 Other specified congenital malformations of intestine	0.003	0.996	0.000
Q67.6 Pectus excavatum	0.003	0.996	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.003	0.996	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.003	0.996	0.000
Q78.8 Other specified osteochondrodysplasias	0.003	0.996	0.000
Q78.6 Multiple congenital exostoses	0.003	0.996	0.000
Q78.5 Metaphyseal dysplasia	0.003	0.996	0.000
Q78.4 Enchondromatosis	0.003	0.996	0.000
Q78.3 Progressive diaphyseal dysplasia	0.003	0.996	0.000
Q78.1 Polyostotic fibrous dysplasia	0.003	0.996	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.003	0.996	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.003	0.996	0.000
Z80.9 Family history of malignant neoplasm, unspecified	0.000	0.996	0.004
I89.1 Lymphangitis	0.000	0.997	0.003
Q87.4 Marfan's syndrome	0.003	0.997	0.000
Q45 Other congenital malformations of digestive system	0.003	0.997	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.003	0.997	0.000
Q83.9 Congenital malformation of breast, unspecified	0.003	0.997	0.000
Q83.2 Absent nipple	0.003	0.997	0.000
Q83.0 Congenital absence of breast with absent nipple	0.003	0.997	0.000
I63 Cerebral infarction	0.003	0.997	0.000
S83.3 Tear of articular cartilage of knee, current	0.003	0.997	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.003	0.997	0.000
Q68.5 Congenital bowing of long bones of leg, unspecified	0.003	0.997	0.000
Q68.4 Congenital bowing of tibia and fibula	0.003	0.997	0.000
Q68.3 Congenital bowing of femur	0.003	0.997	0.000
Q68.2 Congenital deformity of knee	0.003	0.997	0.000
Q68.1 Congenital deformity of hand	0.003	0.997	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.003	0.997	0.000
Q69.9 Polydactyly, unspecified	0.003	0.997	0.000
Q69.2 Accessory toe(s)	0.003	0.997	0.000
Q69.1 Accessory thumb(s)	0.003	0.997	0.000
Q69.0 Accessory finger(s)	0.003	0.997	0.000
Q70.9 Syndactyly, unspecified	0.003	0.997	0.000
Q70.4 Polysyndactyly	0.003	0.997	0.000
Q70.3 Webbed toes	0.003	0.997	0.000
Q70.2 Fused toes	0.003	0.997	0.000
Q70.1 Webbed fingers	0.003	0.997	0.000
Q70.0 Fused fingers	0.003	0.997	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.003	0.997	0.000
Q71.8 Other reduction defects of upper limb(s)	0.003	0.997	0.000
Q71.6 Lobster-claw hand	0.003	0.997	0.000
Q71.5 Longitudinal reduction defect of ulna	0.003	0.997	0.000
Q71.4 Longitudinal reduction defect of radius	0.003	0.997	0.000
Q71.3 Congenital absence of hand and finger(s)	0.003	0.997	0.000
Q71.2 Congenital absence of both forearm and hand	0.003	0.997	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.003	0.997	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.003	0.997	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.003	0.997	0.000
Q72.8 Other reduction defects of lower limb(s)	0.003	0.997	0.000
Q72.7 Split foot	0.003	0.997	0.000
Q72.6 Longitudinal reduction defect of fibula	0.003	0.997	0.000
Q72.5 Longitudinal reduction defect of tibia	0.003	0.997	0.000
Q72.4 Longitudinal reduction defect of femur	0.003	0.997	0.000
Q72.3 Congenital absence of foot and toe(s)	0.003	0.997	0.000
Q72.2 Congenital absence of both lower leg and foot	0.003	0.997	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.003	0.997	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.003	0.997	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.003	0.997	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.003	0.997	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.003	0.997	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.003	0.997	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.003	0.997	0.000
Q75.5 Oculomandibular dysostosis	0.003	0.997	0.000
Q75.4 Mandibulofacial dysostosis	0.003	0.997	0.000
Q75.3 Macrocephaly	0.003	0.997	0.000
Q75.2 Hypertelorism	0.003	0.997	0.000
Q75.1 Craniofacial dysostosis	0.003	0.997	0.000
Q75.0 Craniosynostosis	0.003	0.997	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.003	0.997	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.003	0.997	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.003	0.997	0.000
Q77.6 Chondroectodermal dysplasia	0.003	0.997	0.000
Q77.5 Diastrophic dysplasia	0.003	0.997	0.000
Q77.4 Achondroplasia	0.003	0.997	0.000
Q77.3 Chondrodysplasia punctata	0.003	0.997	0.000
Q77.2 Short rib syndrome	0.003	0.997	0.000
Q77.1 Thanatophoric short stature	0.003	0.997	0.000
Q77.0 Achondrogenesis	0.003	0.997	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.003	0.997	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.003	0.997	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.003	0.997	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.003	0.997	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.003	0.997	0.000
Q65.9 Congenital deformity of hip, unspecified	0.003	0.997	0.000
Q65.6 Unstable hip	0.003	0.997	0.000
Q65.5 Congenital subluxation of hip, unspecified	0.003	0.997	0.000
Q65.4 Congenital subluxation of hip, bilateral	0.003	0.997	0.000
Q65.3 Congenital subluxation of hip, unilateral	0.003	0.997	0.000
Q65.2 Congenital dislocation of hip, unspecified	0.003	0.997	0.000
Q65.1 Congenital dislocation of hip, bilateral	0.003	0.997	0.000
Q65.0 Congenital dislocation of hip, unilateral	0.003	0.997	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.003	0.997	0.000
S61.8 Open wound of other parts of wrist and hand	0.000	0.997	0.003
Q04 Other congenital malformations of brain	0.003	0.997	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
Q65.8 Other congenital deformities of hip	0.003	0.997	0.000
Q78.0 Osteogenesis imperfecta	0.003	0.997	0.000
Q67.5 Congenital deformity of spine	0.003	0.997	0.000
Q35 Cleft palate	0.003	0.997	0.000
Q25.1 Coarctation of aorta	0.003	0.997	0.000
Q40 Other congenital malformations of upper alimentary tract	0.003	0.997	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.003	0.997	0.000
M19.04 Primary arthrosis of other joints (Hand)	0.000	0.997	0.003
Z13.9 Special screening examination, unspecified	0.000	0.997	0.003
Q37 Cleft palate with cleft lip	0.003	0.997	0.000
I07.9 Tricuspid valve disease, unspecified	0.003	0.997	0.000
I07.8 Other tricuspid valve diseases	0.003	0.997	0.000
I07.2 Tricuspid stenosis with insufficiency	0.003	0.997	0.000
I07.0 Tricuspid stenosis	0.003	0.997	0.000
M80.00 Postmenopausal osteoporosis with pathological fracture (Multiple sites)	0.003	0.997	0.000
I66.8 Occlusion and stenosis of other cerebral artery	0.003	0.997	0.000
I66.2 Occlusion and stenosis of posterior cerebral artery	0.003	0.997	0.000
I66.1 Occlusion and stenosis of anterior cerebral artery	0.003	0.997	0.000
K75.8 Other specified inflammatory liver diseases	0.003	0.997	0.000
Q43.7 Persistent cloaca	0.003	0.997	0.000
Q43.6 Congenital fistula of rectum and anus	0.003	0.997	0.000
Q43.5 Ectopic anus	0.003	0.997	0.000
Q43.4 Duplication of intestine	0.003	0.997	0.000
Q43.2 Other congenital functional disorders of colon	0.003	0.997	0.000
Q63.0 Accessory kidney	0.003	0.997	0.000
S83.6 Sprain and strain of other and unspecified parts of knee	0.003	0.997	0.000
I66.4 Occlusion and stenosis of multiple and bilateral cerebral arteries	0.003	0.997	0.000
Q05 Spina bifida	0.003	0.997	0.000
Q03 Congenital hydrocephalus	0.003	0.997	0.000
I66.9 Occlusion and stenosis of unspecified cerebral artery	0.003	0.997	0.000
Q83.8 Other congenital malformations of breast	0.003	0.997	0.000
Q90.2 Trisomy 21, translocation	0.003	0.997	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.003	0.997	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.003	0.997	0.000
Q07 Other congenital malformations of nervous system	0.003	0.997	0.000
Q06 Other congenital malformations of spinal cord	0.003	0.997	0.000
Q01 Encephalocele	0.003	0.997	0.000
Q00 Anencephaly and similar malformations	0.003	0.997	0.000
Q02 Microcephaly	0.003	0.997	0.000
Q36 Cleft lip	0.003	0.997	0.000
I89.0 Lymphoedema, not elsewhere classified	0.000	0.997	0.003
Q96.9 Turner's syndrome, unspecified	0.003	0.997	0.000
Q89 Other congenital malformations, not elsewhere classified	0.003	0.997	0.000
Q60-Q64 Congenital malformations of the urinary system	0.003	0.997	0.000
K75 Other inflammatory liver diseases	0.003	0.997	0.000
M10.96 Gout, unspecified (Lower leg)	0.003	0.997	0.000
I63.3 Cerebral infarction due to thrombosis of cerebral arteries	0.003	0.997	0.000
X62.9 Unspecified place	0.000	0.997	0.003
Q25 Congenital malformations of great arteries	0.003	0.997	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.003	0.997	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.003	0.997	0.000
Q43.1 Hirschsprung's disease	0.003	0.997	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.003	0.997	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.003	0.997	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.003	0.997	0.000
I68.8 Other cerebrovascular disorders in diseases classified elsewhere	0.003	0.997	0.000
I68.2 Cerebral arteritis in other diseases classified elsewhere	0.003	0.997	0.000
I68.1 Cerebral arteritis in infectious and parasitic diseases classified elsewhere	0.003	0.997	0.000
I89 Other non-infective disorders of lymphatic vessels and lymph nodes	0.000	0.997	0.003
D22.5 Melanocytic naevi of trunk	0.003	0.997	0.000
Q18 Other congenital malformations of face and neck	0.003	0.997	0.000
Q34 Other congenital malformations of respiratory system	0.003	0.997	0.000
Q33 Congenital malformations of lung	0.003	0.997	0.000
Q32 Congenital malformations of trachea and bronchus	0.003	0.997	0.000
Q31 Congenital malformations of larynx	0.003	0.997	0.000
Q30 Congenital malformations of nose	0.003	0.997	0.000
Q82 Other congenital malformations of skin	0.003	0.997	0.000
Q04.6 Congenital cerebral cysts	0.003	0.997	0.000
N04.9 Unspecified	0.003	0.997	0.000
Q80.9 Congenital ichthyosis, unspecified	0.003	0.997	0.000
Q80.8 Other congenital ichthyosis	0.003	0.997	0.000
Q80.4 Harlequin foetus	0.003	0.997	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.003	0.997	0.000
Q80.2 Lamellar ichthyosis	0.003	0.997	0.000
Q80.1 X-linked ichthyosis	0.003	0.997	0.000
Q80.0 Ichthyosis vulgaris	0.003	0.997	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.003	0.997	0.000
Q81.8 Other epidermolysis bullosa	0.003	0.997	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.003	0.997	0.000
Q81.1 Epidermolysis bullosa letalis	0.003	0.997	0.000
Q81.0 Epidermolysis bullosa simplex	0.003	0.997	0.000
Q82.2 Mastocytosis	0.003	0.997	0.000
Q84.9 Congenital malformation of integument, unspecified	0.003	0.997	0.000
Q84.8 Other specified congenital malformations of integument	0.003	0.997	0.000
Q84.6 Other congenital malformations of nails	0.003	0.997	0.000
Q84.5 Enlarged and hypertrophic nails	0.003	0.997	0.000
Q84.4 Congenital leukonychia	0.003	0.997	0.000
Q84.3 Anonychia	0.003	0.997	0.000
Q84.2 Other congenital malformations of hair	0.003	0.997	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.003	0.997	0.000
Q84.0 Congenital alopecia	0.003	0.997	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.003	0.997	0.000
Q86.2 Dysmorphism due to warfarin	0.003	0.997	0.000
Q86.1 Foetal hydantoin syndrome	0.003	0.997	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.003	0.997	0.000
Q96.8 Other variants of Turner's syndrome	0.003	0.997	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.003	0.997	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.003	0.997	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.003	0.997	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.003	0.997	0.000
Q96.0 Karyotype 45,X	0.003	0.997	0.000
Q74.9 Unspecified congenital malformation of limb(s)	0.003	0.997	0.000
Q74.8 Other specified congenital malformations of limb(s)	0.003	0.997	0.000
Q74.3 Arthrogryposis multiplex congenita	0.003	0.997	0.000
I66.0 Occlusion and stenosis of middle cerebral artery	0.003	0.997	0.000
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.003	0.997	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.003	0.997	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.003	0.997	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.003	0.997	0.000
Q98.7 Male with sex chromosome mosaicism	0.003	0.997	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.003	0.997	0.000
Q98.5 Karyotype 47,XYY	0.003	0.997	0.000
Q98.3 Other male with 46,XX karyotype	0.003	0.997	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.003	0.997	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.003	0.997	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.003	0.997	0.000
Q35.9 Cleft palate, unspecified	0.003	0.997	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.003	0.997	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.003	0.997	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.003	0.997	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.003	0.997	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.003	0.997	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.003	0.997	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.003	0.997	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.003	0.997	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.003	0.997	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.003	0.997	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.003	0.997	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.003	0.997	0.000
Q63 Other congenital malformations of kidney	0.003	0.997	0.000
I07.1 Tricuspid insufficiency	0.003	0.997	0.000
I89.9 Non-infective disorder of lymphatic vessels and lymph nodes, unspecified	0.000	0.997	0.003
Q18.0 Sinus, fistula and cyst of branchial cleft	0.003	0.997	0.000
Q15 Other congenital malformations of eye	0.003	0.997	0.000
I63.8 Other cerebral infarction	0.003	0.997	0.000
K75.0 Abscess of liver	0.003	0.997	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.003	0.997	0.000
Q45.2 Congenital pancreatic cyst	0.003	0.997	0.000
Q45.1 Annular pancreas	0.003	0.997	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.003	0.997	0.000
Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle	0.003	0.997	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.003	0.997	0.000
Q13 Congenital malformations of anterior segment of eye	0.003	0.997	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.003	0.997	0.000
Q22.5 Ebstein's anomaly	0.003	0.997	0.000
Q39 Congenital malformations of oesophagus	0.002	0.997	0.000
I63.6 Cerebral infarction due to cerebral venous thrombosis, nonpyogenic	0.003	0.997	0.000
I63.1 Cerebral infarction due to embolism of precerebral arteries	0.003	0.997	0.000
Q05.4 Unspecified spina bifida with hydrocephalus	0.003	0.997	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.003	0.997	0.000
Q74.1 Congenital malformation of knee	0.002	0.997	0.000
Z96.8 Presence of other specified functional implants	0.003	0.997	0.000
Q17 Other congenital malformations of ear	0.003	0.997	0.000
I68.0 Cerebral amyloid angiopathy	0.002	0.997	0.000
Q91.7 Patau's syndrome, unspecified	0.002	0.997	0.000
Q91.6 Trisomy 13, translocation	0.002	0.997	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.002	0.997	0.000
Q91.3 Edwards' syndrome, unspecified	0.002	0.997	0.000
Q91.2 Trisomy 18, translocation	0.002	0.997	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.002	0.997	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.002	0.997	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.002	0.997	0.000
Q92.7 Triploidy and polyploidy	0.002	0.997	0.000
Q92.6 Extra marker chromosomes	0.002	0.997	0.000
Q92.5 Duplications with other complex rearrangements	0.002	0.997	0.000
Q92.4 Duplications seen only at prometaphase	0.002	0.997	0.000
Q92.3 Minor partial trisomy	0.002	0.997	0.000
Q92.2 Major partial trisomy	0.002	0.997	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.002	0.997	0.000
Q93.9 Deletion from autosomes, unspecified	0.002	0.997	0.000
Q93.8 Other deletions from the autosomes	0.002	0.997	0.000
Q93.7 Deletions with other complex rearrangements	0.002	0.997	0.000
Q93.6 Deletions seen only at prometaphase	0.002	0.997	0.000
Q93.5 Other deletions of part of a chromosome	0.002	0.997	0.000
Q93.4 Deletion of short arm of chromosome 5	0.002	0.997	0.000
Q93.3 Deletion of short arm of chromosome 4	0.002	0.997	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.002	0.997	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.002	0.997	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.002	0.997	0.000
Q95.8 Other balanced rearrangements and structural markers	0.002	0.997	0.000
Q95.5 Individuals with autosomal fragile site	0.002	0.997	0.000
Q95.4 Individuals with marker heterochromatin	0.002	0.997	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.002	0.997	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.002	0.997	0.000
Q95.1 Chromosome inversion in normal individual	0.002	0.997	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.002	0.997	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.002	0.997	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.002	0.997	0.000
Q97.3 Female with 46,XY karyotype	0.002	0.997	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.002	0.997	0.000
Q97.1 Female with more than three X chromosomes	0.002	0.997	0.000
Q97.0 Karyotype 47,XXX	0.002	0.997	0.000
Q24 Other congenital malformations of heart	0.003	0.997	0.000
I63.4 Cerebral infarction due to embolism of cerebral arteries	0.003	0.997	0.000
Y84.6 Urinary catheterisation	0.003	0.997	0.000
Q37.9 Unspecified cleft palate with unilateral cleft lip	0.002	0.997	0.000
Q44.7 Other congenital malformations of liver	0.002	0.997	0.000
Q44.4 Choledochal cyst	0.002	0.997	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.002	0.997	0.000
Q44.2 Atresia of bile ducts	0.002	0.997	0.000
Q44.1 Other congenital malformations of gallbladder	0.002	0.997	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.002	0.997	0.000
Q45.8 Other specified congenital malformations of digestive system	0.002	0.997	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.002	0.997	0.000
I25.1 Atherosclerotic heart disease	0.003	0.997	0.000
Q04.9 Congenital malformation of brain, unspecified	0.002	0.997	0.000
Q04.8 Other specified congenital malformations of brain	0.002	0.997	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