TreeWAS – Variant ID: rs572169

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
M06.00 Seronegative rheumatoid arthritis (Multiple sites)	0.035	0.965	0.000
M06.0 Seronegative rheumatoid arthritis	0.031	0.969	0.000
M06.09 Seronegative rheumatoid arthritis (Site unspecified)	0.030	0.970	0.000
M06.06 Seronegative rheumatoid arthritis (Lower leg)	0.027	0.973	0.000
M06.07 Seronegative rheumatoid arthritis (Ankle and foot)	0.024	0.976	0.000
M06.08 Seronegative rheumatoid arthritis (Other)	0.023	0.977	0.000
M06.05 Seronegative rheumatoid arthritis (Pelvic region and thigh)	0.023	0.977	0.000
M06.04 Seronegative rheumatoid arthritis (Hand)	0.023	0.977	0.000
M06.03 Seronegative rheumatoid arthritis (Forearm)	0.023	0.977	0.000
M06.02 Seronegative rheumatoid arthritis (Upper arm)	0.023	0.977	0.000
M06.01 Seronegative rheumatoid arthritis (Shoulder region)	0.023	0.977	0.000
B97.7 Papillomavirus as the cause of diseases classified to other chapters	0.000	0.983	0.017
K26.9 Unspecified as acute or chronic, without haemorrhage or perforation	0.009	0.991	0.000
B07 Viral warts	0.000	0.992	0.008
N28.8 Other specified disorders of kidney and ureter	0.008	0.992	0.000
M20.5 Other deformities of toe(s) (acquired)	0.007	0.993	0.000
I49.9 Cardiac arrhythmia, unspecified	0.006	0.994	0.000
T78.2 Anaphylactic shock, unspecified	0.000	0.994	0.006
C16.9 Stomach, unspecified	0.005	0.995	0.000
C16 Malignant neoplasm of stomach	0.005	0.995	0.000
Z49.1 Extracorporeal dialysis	0.005	0.995	0.000
E10.4 With neurological complications	0.005	0.995	0.000
E10.2 With renal complications	0.005	0.995	0.000
I49.3 Ventricular premature depolarisation	0.005	0.995	0.000
C16.8 Overlapping lesion of stomach	0.005	0.995	0.000
C16.5 Lesser curvature of stomach, unspecified	0.005	0.995	0.000
S06.50 Traumatic subdural haemorrhage (without open intracranial wound)	0.005	0.995	0.000
C16.3 Pyloric antrum	0.005	0.995	0.000
C16.6 Greater curvature of stomach, unspecified	0.005	0.995	0.000
C16.1 Fundus of stomach	0.004	0.996	0.000
B97 Viral agents as the cause of diseases classified to other chapters	0.000	0.996	0.004
C16.4 Pylorus	0.004	0.996	0.000
E10.3 With ophthalmic complications	0.004	0.996	0.000
T78.1 Other adverse food reactions, not elsewhere classified	0.000	0.996	0.004
T78 Adverse effects, not elsewhere classified	0.000	0.996	0.004
I49 Other cardiac arrhythmias	0.004	0.996	0.000
K26 Duodenal ulcer	0.004	0.996	0.000
C16.0 Cardia	0.004	0.996	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.004	0.996	0.000
T78.3 Angioneurotic oedema	0.000	0.996	0.004
S81.9 Open wound of lower leg, part unspecified	0.004	0.996	0.000
M06 Other rheumatoid arthritis	0.004	0.996	0.000
Q38.6 Other congenital malformations of mouth	0.004	0.996	0.000
K26.7 Chronic without haemorrhage or perforation	0.004	0.996	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.004	0.996	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.004	0.996	0.000
K26.4 Chronic or unspecified with haemorrhage	0.004	0.996	0.000
K26.3 Acute without haemorrhage or perforation	0.004	0.996	0.000
E10 Insulin-dependent diabetes mellitus	0.004	0.996	0.000
I49.8 Other specified cardiac arrhythmias	0.003	0.997	0.000
Q39 Congenital malformations of oesophagus	0.003	0.997	0.000
B97.4 Respiratory synctial virus as the cause of diseases classified to other chapters	0.000	0.997	0.003
C16.2 Body of stomach	0.003	0.997	0.000
B97.6 Parvovirus as the cause of diseases classified to other chapters	0.000	0.997	0.003
B97.5 Reovirus as the cause of diseases classified to other chapters	0.000	0.997	0.003
B97.3 Retrovirus as the cause of diseases classified to other chapters	0.000	0.997	0.003
B97.2 Coronavirus as the cause of diseases classified to other chapters	0.000	0.997	0.003
B97.1 Enterovirus as the cause of diseases classified to other chapters	0.000	0.997	0.003
B97.0 Adenovirus as the cause of diseases classified to other chapters	0.000	0.997	0.003
Q43 Other congenital malformations of intestine	0.003	0.997	0.000
T78.4 Allergy, unspecified	0.000	0.997	0.003
M06.8 Other specified rheumatoid arthritis	0.003	0.997	0.000
K41.9 Unilateral or unspecified femoral hernia, without obstruction or gangrene	0.000	0.997	0.003
Q38.8 Other congenital malformations of pharynx	0.003	0.997	0.000
R00.1 Bradycardia, unspecified	0.003	0.997	0.000
T78.9 Adverse effect, unspecified	0.000	0.997	0.003
C18.0 Caecum	0.003	0.997	0.000
I49.2 Junctional premature depolarisation	0.003	0.997	0.000
K26.2 Acute with both haemorrhage and perforation	0.003	0.997	0.000
Q38.5 Congenital malformations of palate, not elsewhere classified	0.003	0.997	0.000
Q39.6 Diverticulum of oesophagus	0.003	0.997	0.000
Q39.4 Oesophageal web	0.003	0.997	0.000
B08.1 Molluscum contagiosum	0.000	0.997	0.003
I49.1 Atrial premature depolarisation	0.003	0.997	0.000
M06.2 Rheumatoid bursitis	0.003	0.997	0.000
M06.1 Adult-onset Still's disease	0.003	0.997	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.003	0.997	0.000
M06.80 Other specified rheumatoid arthritis (Multiple sites)	0.003	0.997	0.000
E10.1 With ketoacidosis	0.003	0.997	0.000
C69.9 Eye, unspecified	0.003	0.997	0.000
K26.1 Acute with perforation	0.003	0.997	0.000
Q45 Other congenital malformations of digestive system	0.003	0.997	0.000
K26.0 Acute with haemorrhage	0.003	0.997	0.000
Q38.4 Congenital malformations of salivary glands and ducts	0.003	0.997	0.000
Q38.3 Other congenital malformations of tongue	0.003	0.997	0.000
Q38.2 Macroglossia	0.003	0.997	0.000
Q38.1 Ankyloglossia	0.003	0.997	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.003	0.997	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.003	0.997	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.003	0.997	0.000
Q40 Other congenital malformations of upper alimentary tract	0.003	0.997	0.000
C69.3 Choroid	0.003	0.997	0.000
T78.0 Anaphylactic shock due to adverse food reaction	0.000	0.997	0.003
B08 Other viral infections characterised by skin and mucous membrane lesions, not elsewhere classified	0.000	0.997	0.003
E10.7 With multiple complications	0.003	0.997	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.003	0.997	0.000
Q39.8 Other congenital malformations of oesophagus	0.003	0.997	0.000
Q39.5 Congenital dilatation of oesophagus	0.003	0.997	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.003	0.997	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.003	0.997	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.003	0.997	0.000
Q39.0 Atresia of oesophagus without fistula	0.003	0.997	0.000
M84.17 Nonunion of fracture [pseudarthrosis] (Ankle and foot)	0.000	0.997	0.003
I49.4 Other and unspecified premature depolarisation	0.003	0.997	0.000
S06.5 Traumatic subdural haemorrhage	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
K26.6 Chronic or unspecified with both haemorrhage and perforation	0.003	0.997	0.000
N28 Other disorders of kidney and ureter, not elsewhere classified	0.003	0.997	0.000
Q43.3 Congenital malformations of intestinal fixation	0.003	0.997	0.000
Q43.1 Hirschsprung's disease	0.003	0.997	0.000
E10.5 With peripheral circulatory complications	0.003	0.997	0.000
M06.89 Other specified rheumatoid arthritis (Site unspecified)	0.002	0.997	0.000
M06.88 Other specified rheumatoid arthritis (Other)	0.002	0.997	0.000
M06.87 Other specified rheumatoid arthritis (Ankle and foot)	0.002	0.997	0.000
M06.86 Other specified rheumatoid arthritis (Lower leg)	0.002	0.997	0.000
M06.85 Other specified rheumatoid arthritis (Pelvic region and thigh)	0.002	0.997	0.000
M06.84 Other specified rheumatoid arthritis (Hand)	0.002	0.997	0.000
M06.83 Other specified rheumatoid arthritis (Forearm)	0.002	0.997	0.000
M06.82 Other specified rheumatoid arthritis (Upper arm)	0.002	0.997	0.000
M06.81 Other specified rheumatoid arthritis (Shoulder region)	0.002	0.997	0.000
B00-B09 Viral infections characterized by skin and mucous membrane lesions	0.000	0.997	0.003
Q43.8 Other specified congenital malformations of intestine	0.002	0.997	0.000
Q44.5 Other congenital malformations of bile ducts	0.002	0.997	0.000
F11.2 Dependence syndrome	0.003	0.997	0.000
Q44.4 Choledochal cyst	0.002	0.997	0.000
T78.8 Other adverse effects, not elsewhere classified	0.000	0.997	0.002
C69 Malignant neoplasm of eye and adnexa	0.003	0.997	0.000
G55.2 Nerve root and plexus compressions in spondylosis	0.000	0.997	0.003
M06.4 Inflammatory polyarthropathy	0.002	0.997	0.000
K41.3 Unilateral or unspecified femoral hernia, with obstruction, without gangrene	0.000	0.998	0.002
I49.5 Sick sinus syndrome	0.002	0.998	0.000
M06.19 Adult-onset Still's disease (Site unspecified)	0.002	0.998	0.000
M06.18 Adult-onset Still's disease (Other)	0.002	0.998	0.000
M06.17 Adult-onset Still's disease (Ankle and foot)	0.002	0.998	0.000
M06.16 Adult-onset Still's disease (Lower leg)	0.002	0.998	0.000
M06.15 Adult-onset Still's disease (Pelvic region and thigh)	0.002	0.998	0.000
M06.14 Adult-onset Still's disease (Hand)	0.002	0.998	0.000
M06.13 Adult-onset Still's disease (Forearm)	0.002	0.998	0.000
M06.12 Adult-onset Still's disease (Upper arm)	0.002	0.998	0.000
M06.11 Adult-onset Still's disease (Shoulder region)	0.002	0.998	0.000
M06.10 Adult-onset Still's disease (Multiple sites)	0.002	0.998	0.000
M06.29 Rheumatoid bursitis (Site unspecified)	0.002	0.998	0.000
M06.28 Rheumatoid bursitis (Other)	0.002	0.998	0.000
M06.27 Rheumatoid bursitis (Ankle and foot)	0.002	0.998	0.000
M06.26 Rheumatoid bursitis (Lower leg)	0.002	0.998	0.000
M06.25 Rheumatoid bursitis (Pelvic region and thigh)	0.002	0.998	0.000
M06.24 Rheumatoid bursitis (Hand)	0.002	0.998	0.000
M06.23 Rheumatoid bursitis (Forearm)	0.002	0.998	0.000
M06.22 Rheumatoid bursitis (Upper arm)	0.002	0.998	0.000
M06.21 Rheumatoid bursitis (Shoulder region)	0.002	0.998	0.000
M06.20 Rheumatoid bursitis (Multiple sites)	0.002	0.998	0.000
Q44.7 Other congenital malformations of liver	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
Q45.8 Other specified congenital malformations of digestive system	0.002	0.998	0.000
N48.6 Balanitis xerotica obliterans	0.000	0.998	0.002
Q45.9 Congenital malformation of digestive system, unspecified	0.002	0.998	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.002	0.998	0.000
Q45.2 Congenital pancreatic cyst	0.002	0.998	0.000
Q45.1 Annular pancreas	0.002	0.998	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	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
C67.3 Anterior wall of bladder	0.002	0.998	0.000
M06.3 Rheumatoid nodule	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
B08.8 Other specified viral infections characterised by skin and mucous membrane lesions	0.000	0.998	0.002
B08.5 Enteroviral vesicular pharyngitis	0.000	0.998	0.002
B08.4 Enteroviral vesicular stomatitis with exanthem	0.000	0.998	0.002
B08.3 Erythema infectiosum [fifth disease]	0.000	0.998	0.002
B08.2 Exanthema subitum [sixth disease]	0.000	0.998	0.002
B08.0 Other orthopoxvirus infections	0.000	0.998	0.002
C22.1 Intrahepatic bile duct carcinoma	0.002	0.998	0.000
S06.51 Traumatic subdural haemorrhage (with open intracranial wound)	0.002	0.998	0.000
U80.1 Methicillin resistant agent	0.000	0.998	0.002
Z57.2 Occupational exposure to dust	0.002	0.998	0.000
C69.2 Retina	0.002	0.998	0.000
N28.9 Disorder of kidney and ureter, unspecified	0.002	0.998	0.000
C69.6 Orbit	0.002	0.998	0.000
Z31.0 Tuboplasty or vasoplasty after previous sterilisation	0.000	0.998	0.002
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
B06 Rubella [German measles]	0.000	0.998	0.002
B05 Measles	0.000	0.998	0.002
B09 Unspecified viral infection characterised by skin and mucous membrane lesions	0.000	0.998	0.002
B04 Monkeypox	0.000	0.998	0.002
B03 Smallpox	0.000	0.998	0.002
Q44.6 Cystic disease of liver	0.002	0.998	0.000
Q55.6 Other congenital malformations of penis	0.002	0.998	0.000
K41 Femoral hernia	0.000	0.998	0.002
E10.6 With other specified complications	0.002	0.998	0.000
J69.0 Pneumonitis due to food and vomit	0.002	0.998	0.000
Q55 Other congenital malformations of male genital organs	0.002	0.998	0.000
C69.8 Overlapping lesion of eye and adnexa	0.002	0.998	0.000
C69.5 Lachrymal gland and duct	0.002	0.998	0.000
C69.4 Ciliary body	0.002	0.998	0.000
C69.1 Cornea	0.002	0.998	0.000
I49.0 Ventricular fibrillation and flutter	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
M06.48 Inflammatory polyarthropathy (Other)	0.002	0.998	0.000
M06.47 Inflammatory polyarthropathy (Ankle and foot)	0.002	0.998	0.000
M06.46 Inflammatory polyarthropathy (Lower leg)	0.002	0.998	0.000
M06.45 Inflammatory polyarthropathy (Pelvic region and thigh)	0.002	0.998	0.000
M06.44 Inflammatory polyarthropathy (Hand)	0.002	0.998	0.000
M06.43 Inflammatory polyarthropathy (Forearm)	0.002	0.998	0.000
M06.42 Inflammatory polyarthropathy (Upper arm)	0.002	0.998	0.000
M06.41 Inflammatory polyarthropathy (Shoulder region)	0.002	0.998	0.000
C69.0 Conjunctiva	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
E10.0 With coma	0.002	0.998	0.000
C67.4 Posterior wall of bladder	0.002	0.998	0.000
E10.8 With unspecified complications	0.002	0.998	0.000
F80.1 Expressive language disorder	0.002	0.998	0.000
M25.87 Other specified joint disorders (Ankle and foot)	0.002	0.998	0.000
M47.27 Other spondylosis with radiculopathy (Lumbosacral region)	0.000	0.998	0.002
D22.1 Melanocytic naevi of eyelid, including canthus	0.002	0.998	0.000
N28.1 Cyst of kidney, acquired	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
Q38.7 Pharyngeal pouch	0.002	0.998	0.000
C61 Malignant neoplasm of prostate	0.002	0.998	0.000
Q90 Down's syndrome	0.002	0.998	0.000
M06.39 Rheumatoid nodule (Site unspecified)	0.002	0.998	0.000
M06.38 Rheumatoid nodule (Other)	0.002	0.998	0.000
M06.36 Rheumatoid nodule (Lower leg)	0.002	0.998	0.000
M06.35 Rheumatoid nodule (Pelvic region and thigh)	0.002	0.998	0.000
M06.33 Rheumatoid nodule (Forearm)	0.002	0.998	0.000
M06.31 Rheumatoid nodule (Shoulder region)	0.002	0.998	0.000
M06.30 Rheumatoid nodule (Multiple sites)	0.002	0.998	0.000
M06.40 Inflammatory polyarthropathy (Multiple sites)	0.002	0.998	0.000
Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate	0.002	0.998	0.000
H53.0 Amblyopia ex anopsia	0.000	0.998	0.002
G82.2 Paraplegia, unspecified	0.002	0.998	0.000
R52.1 Chronic intractable pain	0.002	0.998	0.000
U51.1 Previously admitted to a psychiatric hospital of the provider	0.000	0.998	0.002
Q12 Congenital lens malformations	0.002	0.998	0.000
Q30 Congenital malformations of nose	0.002	0.998	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.002	0.998	0.000
S67.0 Crushing injury of thumb and other finger(s)	0.000	0.998	0.002
F11 Mental and behavioural disorders due to use of opioids	0.002	0.998	0.000
Q12.0 Congenital cataract	0.002	0.998	0.000
K26.5 Chronic or unspecified with perforation	0.002	0.998	0.000
Q82.0 Hereditary lymphoedema	0.002	0.998	0.000
Q90.9 Down's syndrome, unspecified	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.002	0.998	0.000
C24.0 Extrahepatic bile duct	0.002	0.998	0.000
O00.9 Ectopic pregnancy, unspecified	0.002	0.998	0.000
Q30.3 Congenital perforated nasal septum	0.002	0.998	0.000
B01 Varicella [chickenpox]	0.000	0.998	0.002
C67 Malignant neoplasm of bladder	0.002	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
C67.1 Dome of bladder	0.002	0.998	0.000
N18.2 Chronic kidney disease, stage 2	0.002	0.998	0.000
Q82 Other congenital malformations of skin	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
M06.34 Rheumatoid nodule (Hand)	0.002	0.998	0.000
B05.9 Measles without complication	0.000	0.998	0.002
B05.8 Measles with other complications	0.000	0.998	0.002
B05.4 Measles with intestinal complications	0.000	0.998	0.002
B05.3 Measles complicated by otitis media	0.000	0.998	0.002
B05.2 Measles complicated by pneumonia	0.000	0.998	0.002
B05.1 Measles complicated by meningitis	0.000	0.998	0.002
B05.0 Measles complicated by encephalitis	0.000	0.998	0.002
B06.9 Rubella without complication	0.000	0.998	0.002
B06.8 Rubella with other complications	0.000	0.998	0.002
B06.0 Rubella with neurological complications	0.000	0.998	0.002
F11.3 Withdrawal state	0.002	0.998	0.000
K41.4 Unilateral or unspecified femoral hernia, with gangrene	0.000	0.998	0.002
K41.1 Bilateral femoral hernia, with gangrene	0.000	0.998	0.002
K41.0 Bilateral femoral hernia, with obstruction, without gangrene	0.000	0.998	0.002
Q43.0 Meckel's diverticulum	0.002	0.998	0.000
Q50.4 Embryonic cyst of Fallopian tube	0.002	0.998	0.000
Q78.0 Osteogenesis imperfecta	0.002	0.998	0.000
Q10.0 Congenital ptosis	0.002	0.998	0.000
Q55.9 Congenital malformation of male genital organ, unspecified	0.002	0.998	0.000
Q55.8 Other specified congenital malformations of male genital organs	0.002	0.998	0.000
Q55.5 Congenital absence and aplasia of penis	0.002	0.998	0.000
Q55.3 Atresia of vas deferens	0.002	0.998	0.000
Q55.1 Hypoplasia of testis and scrotum	0.002	0.998	0.000
Q55.0 Absence and aplasia of testis	0.002	0.998	0.000
Q31 Congenital malformations of larynx	0.002	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	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
Q11.1 Other anophthalmos	0.002	0.998	0.000
F15.1 Harmful use	0.002	0.998	0.000
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
U80 Agent resistant to penicillin and related antibiotics	0.000	0.998	0.002
F11.1 Harmful use	0.002	0.998	0.000
Q82.8 Other specified congenital malformations of skin	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
Q27 Other congenital malformations of peripheral vascular system	0.002	0.998	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	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
M06.32 Rheumatoid nodule (Upper arm)	0.001	0.998	0.000
B34.9 Viral infection, unspecified	0.002	0.998	0.000
G52.8 Disorders of other specified cranial nerves	0.002	0.998	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.002	0.998	0.000
U80.0 Penicillin resistant agent	0.000	0.998	0.002
Y51.7 Beta-Adrenoreceptor antagonists, not elsewhere classified	0.002	0.998	0.000
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
M25.61 Stiffness of joint, not elsewhere classified (Shoulder region)	0.000	0.998	0.002
C67.6 Ureteric orifice	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
Q14 Congenital malformations of posterior segment of eye	0.002	0.998	0.000
Q13 Congenital malformations of anterior segment of eye	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
Q90.2 Trisomy 21, translocation	0.001	0.998	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.001	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
M06.37 Rheumatoid nodule (Ankle and foot)	0.001	0.998	0.000
M06.49 Inflammatory polyarthropathy (Site unspecified)	0.001	0.998	0.000
M84.14 Nonunion of fracture [pseudarthrosis] (Hand)	0.000	0.998	0.002
Q22.1 Congenital pulmonary valve stenosis	0.002	0.998	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.998	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.002	0.998	0.000
Q15 Other congenital malformations of eye	0.002	0.998	0.000
M47.92 Spondylosis, unspecified (Cervical region)	0.002	0.998	0.000
M79.67 Pain in limb (Ankle and foot)	0.002	0.998	0.000
Q12.9 Congenital lens malformation, unspecified	0.001	0.998	0.000
Q12.8 Other congenital lens malformations	0.001	0.998	0.000
Q12.4 Spherophakia	0.001	0.998	0.000
Q12.3 Congenital aphakia	0.001	0.998	0.000
Q12.2 Coloboma of lens	0.001	0.998	0.000
Q12.1 Congenital displaced lens	0.001	0.998	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.002	0.998	0.000
Q30.9 Congenital malformation of nose, unspecified	0.001	0.998	0.000
Q30.8 Other congenital malformations of nose	0.001	0.998	0.000
Q30.2 Fissured, notched and cleft nose	0.001	0.998	0.000
Q30.1 Agenesis and underdevelopment of nose	0.001	0.998	0.000
Q30.0 Choanal atresia	0.001	0.998	0.000
Q50.5 Embryonic cyst of broad ligament	0.002	0.998	0.000
F11.9 Unspecified mental and behavioural disorder	0.001	0.998	0.000
F11.8 Other mental and behavioural disorders	0.001	0.998	0.000
F11.7 Residual and late-onset psychotic disorder	0.001	0.998	0.000
F11.6 Amnesic syndrome	0.001	0.998	0.000
F11.5 Psychotic disorder	0.001	0.998	0.000
F11.4 Withdrawal state with delirium	0.001	0.998	0.000
F11.0 Acute intoxication	0.001	0.998	0.000
C67.0 Trigone of bladder	0.002	0.998	0.000
K41.2 Bilateral femoral hernia, without obstruction or gangrene	0.000	0.998	0.001
Q27.3 Peripheral arteriovenous malformation	0.002	0.998	0.000
Q51.3 Bicornate uterus	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.001	0.998	0.000
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
Q96 Turner's syndrome	0.001	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
M19.17 Post-traumatic arthrosis of other joints (Ankle and foot)	0.002	0.998	0.000
B01.8 Varicella with other complications	0.000	0.998	0.001
B01.2 Varicella pneumonia	0.000	0.998	0.001
B01.1 Varicella encephalitis	0.000	0.998	0.001
B01.0 Varicella meningitis	0.000	0.998	0.001
B97.8 Other viral agents as the cause of diseases classified to other chapters	0.000	0.998	0.001
C67.7 Urachus	0.001	0.998	0.000
Q10.7 Congenital malformation of orbit	0.001	0.998	0.000
Q10.6 Other congenital malformations of lachrymal apparatus	0.001	0.998	0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct	0.001	0.998	0.000
Q10.4 Absence and agenesis of lachrymal apparatus	0.001	0.998	0.000
Q10.3 Other congenital malformations of eyelid	0.001	0.998	0.000
Q10.2 Congenital entropion	0.001	0.998	0.000
Q10.1 Congenital ectropion	0.001	0.998	0.000
Q11.3 Macrophthalmos	0.001	0.998	0.000
Q11.2 Microphthalmos	0.001	0.998	0.000
Q11.0 Cystic eyeball	0.001	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.001	0.998	0.000
Q31.0 Web of larynx	0.001	0.998	0.000
Q50.6 Other congenital malformatons of Fallopian tube and broad ligament	0.001	0.998	0.000
Q50.3 Other congenital malformations of ovary	0.001	0.998	0.000
Q50.2 Congenital torsion of ovary	0.001	0.998	0.000
Q50.1 Developmental ovarian cyst	0.001	0.998	0.000
Q50.0 Congenital absence of ovary	0.001	0.998	0.000
Q66.8 Other congenital deformities of feet	0.002	0.998	0.000
Q82.5 Congenital nonneoplastic naevus	0.002	0.998	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.001	0.998	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.001	0.998	0.000
Q84 Other congenital malformations of integument	0.001	0.998	0.000
Q81 Epidermolysis bullosa	0.001	0.998	0.000
Q80 Congenital ichthyosis	0.001	0.998	0.000
U51 Admission status on psychiatric patients	0.000	0.998	0.002
D22.0 Melanocytic naevi of lip	0.002	0.998	0.000
K81.0 Acute cholecystitis	0.002	0.998	0.000
Q82.9 Congenital malformation of skin, unspecified	0.001	0.998	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.001	0.998	0.000
Q82.3 Incontinentia pigmenti	0.001	0.998	0.000
Q82.1 Xeroderma pigmentosum	0.001	0.998	0.000
S83.5 Sprain and strain involving (anterior)(posterior) cruciate ligament of knee	0.002	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
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
I72.4 Aneurysm of artery of lower extremity	0.002	0.998	0.000
Q17 Other congenital malformations of ear	0.001	0.998	0.000
Q25 Congenital malformations of great arteries	0.001	0.998	0.000
Q35 Cleft palate	0.001	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.001	0.998	0.000
C67.8 Overlapping lesion of bladder	0.001	0.998	0.000
Q31.9 Congenital malformation of larynx, unspecified	0.001	0.998	0.000
Q31.8 Other congenital malformations of larynx	0.001	0.998	0.000
Q31.5 Congenital laryngomalacia	0.001	0.998	0.000
Q31.4 Congenital laryngeal stridor	0.001	0.998	0.000
Q31.3 Laryngocele	0.001	0.998	0.000
Q31.2 Laryngeal hypoplasia	0.001	0.998	0.000
Q31.1 Congenital subglottic stenosis	0.001	0.998	0.000
Q78.2 Osteopetrosis	0.001	0.998	0.000
Q91.7 Patau's syndrome, unspecified	0.001	0.998	0.000
Q91.6 Trisomy 13, translocation	0.001	0.998	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.001	0.998	0.000
Q91.3 Edwards' syndrome, unspecified	0.001	0.998	0.000
Q91.2 Trisomy 18, translocation	0.001	0.998	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.001	0.998	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.001	0.998	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.001	0.998	0.000
Q92.7 Triploidy and polyploidy	0.001	0.998	0.000
Q92.6 Extra marker chromosomes	0.001	0.998	0.000
Q92.5 Duplications with other complex rearrangements	0.001	0.998	0.000
Q92.4 Duplications seen only at prometaphase	0.001	0.998	0.000
Q92.3 Minor partial trisomy	0.001	0.998	0.000
Q92.2 Major partial trisomy	0.001	0.998	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.001	0.998	0.000
Q93.9 Deletion from autosomes, unspecified	0.001	0.998	0.000
Q93.8 Other deletions from the autosomes	0.001	0.998	0.000
Q93.7 Deletions with other complex rearrangements	0.001	0.998	0.000
Q93.6 Deletions seen only at prometaphase	0.001	0.998	0.000
Q93.5 Other deletions of part of a chromosome	0.001	0.998	0.000
Q93.4 Deletion of short arm of chromosome 5	0.001	0.998	0.000
Q93.3 Deletion of short arm of chromosome 4	0.001	0.998	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.001	0.998	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.001	0.998	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.001	0.998	0.000
Q95.8 Other balanced rearrangements and structural markers	0.001	0.998	0.000
Q95.5 Individuals with autosomal fragile site	0.001	0.998	0.000
Q95.4 Individuals with marker heterochromatin	0.001	0.998	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.001	0.998	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.001	0.998	0.000
Q95.1 Chromosome inversion in normal individual	0.001	0.998	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.001	0.998	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.001	0.998	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.001	0.998	0.000
Q97.3 Female with 46,XY karyotype	0.001	0.998	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.001	0.998	0.000
Q97.1 Female with more than three X chromosomes	0.001	0.998	0.000
Q97.0 Karyotype 47,XXX	0.001	0.998	0.000
Q99.9 Chromosomal abnormality, unspecified	0.001	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.001	0.998	0.000
Q99.2 Fragile X chromosome	0.001	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.001	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.001	0.998	0.000
S05.1 Contusion of eyeball and orbital tissues	0.000	0.998	0.002
Z11.2 Special screening examination for other bacterial diseases	0.002	0.998	0.000
C22 Malignant neoplasm of liver and intrahepatic bile ducts	0.002	0.998	0.000
Q23 Congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.001	0.998	0.000
Q78.8 Other specified osteochondrodysplasias	0.001	0.998	0.000
Q78.6 Multiple congenital exostoses	0.001	0.998	0.000
Q78.5 Metaphyseal dysplasia	0.001	0.998	0.000
Q78.4 Enchondromatosis	0.001	0.998	0.000
Q78.3 Progressive diaphyseal dysplasia	0.001	0.998	0.000
Q78.1 Polyostotic fibrous dysplasia	0.001	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