TreeWAS – Variant ID: rs9865818

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
E03.9 Hypothyroidism, unspecified	0.000	0.000	1.000
K90.0 Coeliac disease	0.000	0.001	0.999
C44 Other malignant neoplasms of skin	0.999	0.001	0.000
C44.3 Skin of other and unspecified parts of face	0.994	0.006	0.000
C44.4 Skin of scalp and neck	0.978	0.022	0.000
C44.1 Skin of eyelid, including canthus	0.977	0.023	0.000
C44.9 Malignant neoplasm of skin, unspecified	0.969	0.031	0.000
C44.7 Skin of lower limb, including hip	0.968	0.032	0.000
C44.0 Skin of lip	0.912	0.088	0.000
C44.6 Skin of upper limb, including shoulder	0.792	0.208	0.000
C44.8 Overlapping lesion of skin	0.716	0.284	0.000
C44.5 Skin of trunk	0.710	0.290	0.000
C44.2 Skin of ear and external auricular canal	0.682	0.318	0.000
K90 Intestinal malabsorption	0.000	0.554	0.446
E03 Other hypothyroidism	0.000	0.583	0.417
K90.8 Other intestinal malabsorption	0.000	0.641	0.359
C43-C44 Melanoma and other malignant neoplasms of skin	0.344	0.656	0.000
K90.3 Pancreatic steatorrhoea	0.000	0.680	0.320
K90.2 Blind loop syndrome, not elsewhere classified	0.000	0.680	0.320
K90.1 Tropical sprue	0.000	0.680	0.320
E03.1 Congenital hypothyroidism without goitre	0.000	0.693	0.307
K90.4 Malabsorption due to intolerance, not elsewhere classified	0.000	0.697	0.303
E03.0 Congenital hypothyroidism with diffuse goitre	0.000	0.699	0.301
E03.5 Myxoedema coma	0.000	0.701	0.299
E03.4 Atrophy of thyroid (acquired)	0.000	0.701	0.299
E03.3 Postinfectious hypothyroidism	0.000	0.701	0.299
K90.9 Intestinal malabsorption, unspecified	0.000	0.721	0.279
E03.8 Other specified hypothyroidism	0.000	0.724	0.276
E03.2 Hypothyroidism due to medicaments and other exogenous substances	0.000	0.732	0.268
C43 Malignant melanoma of skin	0.211	0.789	0.000
C43.3 Malignant melanoma of other and unspecified parts of face	0.179	0.821	0.000
C43.9 Malignant melanoma of skin, unspecified	0.169	0.831	0.000
C43.1 Malignant melanoma of eyelid, including canthus	0.167	0.833	0.000
C43.4 Malignant melanoma of scalp and neck	0.163	0.837	0.000
C43.8 Overlapping malignant melanoma of skin	0.151	0.849	0.000
C43.0 Malignant melanoma of lip	0.151	0.849	0.000
C43.2 Malignant melanoma of ear and external auricular canal	0.143	0.856	0.000
C43.6 Malignant melanoma of upper limb, including shoulder	0.140	0.860	0.000
E00-E07 Disorders of thyroid gland	0.000	0.883	0.117
Z43.3 Attention to colostomy	0.000	0.883	0.117
E07 Other disorders of thyroid	0.000	0.889	0.111
C43.7 Malignant melanoma of lower limb, including hip	0.110	0.890	0.000
E07.8 Other specified disorders of thyroid	0.000	0.901	0.099
E07.9 Disorder of thyroid, unspecified	0.000	0.903	0.097
E01 Iodine-deficiency-related thyroid disorders and allied conditions	0.000	0.916	0.084
E00 Congenital iodine-deficiency syndrome	0.000	0.916	0.084
E06 Thyroiditis	0.000	0.916	0.084
E02 Subclinical iodine-deficiency hypothyroidism	0.000	0.918	0.082
E07.1 Dyshormogenetic goitre	0.000	0.920	0.079
E07.0 Hypersecretion of calcitonin	0.000	0.920	0.079
E06.5 Other chronic thyroiditis	0.000	0.937	0.063
E06.3 Autoimmune thyroiditis	0.000	0.939	0.061
E00.9 Congenital iodine-deficiency syndrome, unspecified	0.000	0.939	0.060
E00.2 Congenital iodine-deficiency syndrome, mixed type	0.000	0.939	0.060
E00.1 Congenital iodine-deficiency syndrome, myxoedematous type	0.000	0.939	0.060
E00.0 Congenital iodine-deficiency syndrome, neurological type	0.000	0.939	0.060
E01.8 Other iodine-deficiency-related thyroid disorders and allied conditions	0.000	0.939	0.060
E01.2 Iodine-deficiency-related (endemic) goitre, unspecified	0.000	0.939	0.060
E01.1 Iodine-deficiency-related multinodular (endemic) goitre	0.000	0.939	0.060
E01.0 Iodine-deficiency-related diffuse (endemic) goitre	0.000	0.939	0.060
E06.4 Drug-induced thyroiditis	0.000	0.939	0.060
E06.2 Chronic thyroiditis with transient thyrotoxicosis	0.000	0.939	0.060
E06.0 Acute thyroiditis	0.000	0.939	0.060
E06.1 Subacute thyroiditis	0.000	0.941	0.059
E06.9 Thyroiditis, unspecified	0.000	0.941	0.059
K90-K93 Other diseases of the digestive system	0.000	0.942	0.058
K93 Disorders of other digestive organs in diseases classified elsewhere	0.000	0.958	0.042
C80.9 Malignant neoplasm, unspecified	0.037	0.963	0.000
K91 Postprocedural disorders of digestive system, not elsewhere classified	0.000	0.965	0.035
K91.8 Other postprocedural disorders of digestive system, not elsewhere classified	0.000	0.969	0.031
K93.8 Disorders of other specified digestive organs in diseases classified elsewhere	0.000	0.970	0.030
K93.1 Megacolon in Chagas' disease	0.000	0.970	0.030
K93.0 Tuberculous disorders of intestines, peritoneum and mesenteric glands	0.000	0.970	0.030
K91.4 Colostomy and enterostomy malfunction	0.000	0.973	0.027
E04 Other non-toxic goitre	0.000	0.973	0.027
K91.2 Postsurgical malabsorption, not elsewhere classified	0.000	0.973	0.027
K91.0 Vomiting following gastro-intestinal surgery	0.000	0.974	0.026
K91.1 Postgastric surgery syndromes	0.000	0.975	0.025
C80 Malignant neoplasm without specification of site	0.025	0.975	0.000
C80.0 Malignant neoplasm, primary site unknown, so stated	0.023	0.977	0.000
E04.2 Non-toxic multinodular goitre	0.000	0.978	0.022
C43.5 Malignant melanoma of trunk	0.022	0.978	0.000
K91.5 Postcholecystectomy syndrome	0.000	0.980	0.020
E04.8 Other specified non-toxic goitre	0.000	0.980	0.020
K91.9 Postprocedural disorder of digestive system, unspecified	0.000	0.982	0.018
E04.0 Non-toxic diffuse goitre	0.000	0.983	0.017
E05 Thyrotoxicosis [hyperthyroidism]	0.000	0.983	0.016
Q61.3 Polycystic kidney, unspecified	0.012	0.988	0.000
E05.5 Thyroid crisis or storm	0.000	0.988	0.012
E05.4 Thyrotoxicosis factitia	0.000	0.988	0.012
E05.3 Thyrotoxicosis from ectopic thyroid tissue	0.000	0.988	0.012
Q28.2 Arteriovenous malformation of cerebral vessels	0.012	0.988	0.000
E05.1 Thyrotoxicosis with toxic single thyroid nodule	0.000	0.989	0.011
E05.0 Thyrotoxicosis with diffuse goitre	0.000	0.989	0.011
Q24 Other congenital malformations of heart	0.011	0.989	0.000
Q28 Other congenital malformations of circulatory system	0.011	0.989	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.011	0.989	0.000
E05.2 Thyrotoxicosis with toxic multinodular goitre	0.000	0.990	0.010
Q24.6 Congenital heart block	0.010	0.990	0.000
Q24.5 Malformation of coronary vessels	0.010	0.990	0.000
N81.8 Other female genital prolapse	0.010	0.990	0.000
Z43 Attention to artificial openings	0.000	0.991	0.009
Q61 Cystic kidney disease	0.009	0.991	0.000
Q24.4 Congenital subaortic stenosis	0.009	0.991	0.000
Q26 Congenital malformations of great veins	0.009	0.991	0.000
Q27 Other congenital malformations of peripheral vascular system	0.009	0.991	0.000
Q24.8 Other specified congenital malformations of heart	0.009	0.991	0.000
Q27.3 Peripheral arteriovenous malformation	0.008	0.992	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.008	0.992	0.000
Q60-Q64 Congenital malformations of the urinary system	0.008	0.992	0.000
Q24.0 Dextrocardia	0.008	0.992	0.000
Q24.3 Pulmonary infundibular stenosis	0.008	0.992	0.000
Q24.2 Cor triatriatum	0.008	0.992	0.000
Q24.1 Levocardia	0.008	0.992	0.000
Q00-Q07 Congenital malformations of the nervous system	0.008	0.992	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.008	0.992	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.008	0.992	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.008	0.992	0.000
Q28.1 Other malformations of precerebral vessels	0.008	0.992	0.000
Q28.3 Other malformations of cerebral vessels	0.008	0.992	0.000
E27.4 Other and unspecified adrenocortical insufficiency	0.000	0.992	0.008
I77.1 Stricture of artery	0.000	0.992	0.008
Q28.0 Arteriovenous malformation of precerebral vessels	0.008	0.992	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.008	0.992	0.000
E27 Other disorders of adrenal gland	0.000	0.992	0.008
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.008	0.992	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.008	0.992	0.000
Z43.5 Attention to cyctostomy	0.000	0.992	0.008
Z43.0 Attention to tracheostomy	0.000	0.992	0.008
Q05 Spina bifida	0.007	0.993	0.000
E27.1 Primary adrenocortical insufficiency	0.000	0.993	0.007
Q61.2 Polycystic kidney, adult type	0.007	0.993	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.007	0.993	0.000
Chapter IV Endocrine, nutritional and metabolic diseases	0.000	0.993	0.007
E28 Ovarian dysfunction	0.000	0.993	0.007
E55.9 Vitamin D deficiency, unspecified	0.000	0.993	0.007
Q23 Congenital malformations of aortic and mitral valves	0.007	0.993	0.000
Q61.9 Cystic kidney disease, unspecified	0.007	0.993	0.000
E28.2 Polycystic ovarian syndrome	0.000	0.993	0.007
Q05.9 Spina bifida, unspecified	0.007	0.993	0.000
Z43.9 Attention to unspecified artificial opening	0.000	0.993	0.007
Z43.7 Attention to artificial vagina	0.000	0.993	0.007
Z43.1 Attention to gastrostomy	0.000	0.993	0.007
E28.3 Primary ovarian failure	0.000	0.993	0.007
Q04 Other congenital malformations of brain	0.007	0.993	0.000
Q64 Other congenital malformations of urinary system	0.007	0.993	0.000
Q61.8 Other cystic kidney diseases	0.007	0.993	0.000
Q61.1 Polycystic kidney, infantile type	0.007	0.993	0.000
E27.3 Drug-induced adrenocortical insufficiency	0.000	0.993	0.007
Q96 Turner's syndrome	0.007	0.993	0.000
E55 Vitamin D deficiency	0.000	0.993	0.007
Q26.9 Congenital malformation of great vein, unspecified	0.006	0.993	0.000
Q26.8 Other congenital malformations of great veins	0.006	0.993	0.000
Q26.6 Portal vein-hepatic artery fistula	0.006	0.993	0.000
Q26.5 Anomalous portal venous connexion	0.006	0.993	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.006	0.993	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.006	0.993	0.000
Q26.1 Persistent left superior vena cava	0.006	0.993	0.000
Q26.0 Congenital stenosis of vena cava	0.006	0.993	0.000
E20-E35 Disorders of other endocrine glands	0.000	0.993	0.007
Q27.4 Congenital phlebectasia	0.006	0.993	0.000
Q27.2 Other congenital malformations of renal artery	0.006	0.993	0.000
Q27.1 Congenital renal artery stenosis	0.006	0.993	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.006	0.993	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.006	0.993	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.006	0.993	0.000
Q25 Congenital malformations of great arteries	0.006	0.994	0.000
E50-E64 Other nutritional deficiencies	0.000	0.994	0.006
Q27.8 Other specified congenital malformations of peripheral vascular system	0.006	0.994	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.006	0.994	0.000
L98.0 Pyogenic granuloma	0.006	0.994	0.000
S46.0 Injury of tendon of the rotator cuff of shoulder	0.006	0.994	0.000
Q03 Congenital hydrocephalus	0.006	0.994	0.000
Q61.4 Renal dysplasia	0.006	0.994	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.006	0.994	0.000
Q07 Other congenital malformations of nervous system	0.006	0.994	0.000
E05.8 Other thyrotoxicosis	0.001	0.994	0.005
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.006	0.994	0.000
Q96.9 Turner's syndrome, unspecified	0.006	0.994	0.000
Q06 Other congenital malformations of spinal cord	0.006	0.994	0.000
Q01 Encephalocele	0.006	0.994	0.000
Q00 Anencephaly and similar malformations	0.006	0.994	0.000
Q02 Microcephaly	0.006	0.994	0.000
Q04.6 Congenital cerebral cysts	0.006	0.994	0.000
Z43.8 Attention to other artificial openings	0.000	0.994	0.006
Q50-Q56 Congenital malformations of genital organs	0.006	0.994	0.000
Q99.8 Other specified chromosome abnormalities	0.006	0.994	0.000
E27.2 Addisonian crisis	0.000	0.994	0.006
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.006	0.994	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.006	0.994	0.000
Q20.6 Isomerism of atrial appendages	0.006	0.994	0.000
Q20.5 Discordant atrioventricular connexion	0.006	0.994	0.000
Q20.4 Double inlet ventricle	0.006	0.994	0.000
Q20.3 Discordant ventriculoarterial connexion	0.006	0.994	0.000
Q20.2 Double outlet left ventricle	0.006	0.994	0.000
Q20.1 Double outlet right ventricle	0.006	0.994	0.000
Q20.0 Common arterial trunk	0.006	0.994	0.000
E04.1 Non-toxic single thyroid nodule	0.000	0.994	0.006
E27.5 Adrenomedullary hyperfunction	0.000	0.994	0.006
E27.0 Other adrenocortical overactivity	0.000	0.994	0.006
Q05.4 Unspecified spina bifida with hydrocephalus	0.006	0.994	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.006	0.994	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.006	0.994	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.006	0.994	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.006	0.994	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.006	0.994	0.000
Q80-Q89 Other congenital malformations	0.006	0.994	0.000
Q35-Q37 Cleft lip and cleft palate	0.006	0.994	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.006	0.994	0.000
Q23.3 Congenital mitral insufficiency	0.005	0.994	0.000
Q05.8 Sacral spina bifida without hydrocephalus	0.005	0.994	0.000
Q05.6 Thoracic spina bifida without hydrocephalus	0.005	0.994	0.000
Q05.5 Cervical spina bifida without hydrocephalus	0.005	0.994	0.000
Q05.3 Sacral spina bifida with hydrocephalus	0.005	0.994	0.000
Q05.2 Lumbar spina bifida with hydrocephalus	0.005	0.994	0.000
Q05.1 Thoracic spina bifida with hydrocephalus	0.005	0.994	0.000
Q05.0 Cervical spina bifida with hydrocephalus	0.005	0.994	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.005	0.994	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.005	0.994	0.000
Q22.6 Hypoplastic right heart syndrome	0.005	0.994	0.000
Q22.5 Ebstein's anomaly	0.005	0.994	0.000
Q22.4 Congenital tricuspid stenosis	0.005	0.994	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.005	0.994	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.005	0.994	0.000
Q22.0 Pulmonary valve atresia	0.005	0.994	0.000
Q23.0 Congenital stenosis of aortic valve	0.005	0.994	0.000
Q90 Down's syndrome	0.005	0.994	0.000
E23 Hypofunction and other disorders of pituitary gland	0.000	0.994	0.006
Q05.7 Lumbar spina bifida without hydrocephalus	0.005	0.994	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.005	0.994	0.000
Q61.5 Medullary cystic kidney	0.005	0.994	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.005	0.994	0.000
E28.9 Ovarian dysfunction, unspecified	0.000	0.994	0.005
E28.8 Other ovarian dysfunction	0.000	0.994	0.005
E28.1 Androgen excess	0.000	0.994	0.005
E28.0 Oestrogen excess	0.000	0.994	0.005
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.005	0.995	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.005	0.995	0.000
Q23.4 Hypoplastic left heart syndrome	0.005	0.995	0.000
Q23.2 Congenital mitral stenosis	0.005	0.995	0.000
Q14 Congenital malformations of posterior segment of eye	0.005	0.995	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.005	0.995	0.000
Q21 Congenital malformations of cardiac septa	0.005	0.995	0.000
Q60.0 Renal agenesis, unilateral	0.005	0.995	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.005	0.995	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.005	0.995	0.000
E27.8 Other specified disorders of adrenal gland	0.000	0.995	0.005
Q15 Other congenital malformations of eye	0.005	0.995	0.000
Q52 Other congenital malformations of female genitalia	0.005	0.995	0.000
Q25.3 Stenosis of aorta	0.005	0.995	0.000
M05.90 Seropositive rheumatoid arthritis, unspecified (Multiple sites)	0.005	0.995	0.000
Q04.9 Congenital malformation of brain, unspecified	0.005	0.995	0.000
Q04.8 Other specified congenital malformations of brain	0.005	0.995	0.000
Q04.5 Megalencephaly	0.005	0.995	0.000
Q04.4 Septo-optic dysplasia	0.005	0.995	0.000
Q04.3 Other reduction deformities of brain	0.005	0.995	0.000
Q04.2 Holoprosencephaly	0.005	0.995	0.000
Q04.1 Arhinencephaly	0.005	0.995	0.000
Q04.0 Congenital malformations of corpus callosum	0.005	0.995	0.000
Q22.1 Congenital pulmonary valve stenosis	0.005	0.995	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.005	0.995	0.000
Q64.8 Other specified congenital malformations of urinary system	0.005	0.995	0.000
Q64.6 Congenital diverticulum of bladder	0.005	0.995	0.000
Q64.5 Congenital absence of bladder and urethra	0.005	0.995	0.000
Q64.4 Malformation of urachus	0.005	0.995	0.000
Q64.2 Congenital posterior urethral valves	0.005	0.995	0.000
Q64.1 Exstrophy of urinary bladder	0.005	0.995	0.000
Q64.0 Epispadias	0.005	0.995	0.000
E58 Dietary calcium deficiency	0.000	0.995	0.005
E40-E46 Malnutrition	0.000	0.995	0.005
Q96.8 Other variants of Turner's syndrome	0.005	0.995	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.005	0.995	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.005	0.995	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.005	0.995	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.005	0.995	0.000
Q96.0 Karyotype 45,X	0.005	0.995	0.000
E56 Other vitamin deficiencies	0.000	0.995	0.005
E55.0 Rickets, active	0.000	0.995	0.005
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.005	0.995	0.000
E35 Disorders of endocrine glands in diseases classified elsewhere	0.000	0.995	0.005
E31 Polyglandular dysfunction	0.000	0.995	0.005
E30 Disorders of puberty, not elsewhere classified	0.000	0.995	0.005
Q25.7 Other congenital malformations of pulmonary artery	0.005	0.995	0.000
E51 Thiamine deficiency	0.000	0.995	0.005
Q17 Other congenital malformations of ear	0.005	0.995	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.005	0.995	0.000
Q99.9 Chromosomal abnormality, unspecified	0.005	0.995	0.000
Q99.2 Fragile X chromosome	0.005	0.995	0.000
Q99.1 46,XX true hermaphrodite	0.005	0.995	0.000
Q99.0 Chimera 46,XX/46,XY	0.005	0.995	0.000
Q60.6 Potter's syndrome	0.005	0.995	0.000
Q60.5 Renal hypoplasia, unspecified	0.005	0.995	0.000
Q60.4 Renal hypoplasia, bilateral	0.005	0.995	0.000
Q60.3 Renal hypoplasia, unilateral	0.005	0.995	0.000
Q60.1 Renal agenesis, bilateral	0.005	0.995	0.000
E25 Adrenogenital disorders	0.000	0.995	0.005
Q03.0 Malformations of aqueduct of Sylvius	0.005	0.995	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.005	0.995	0.000
Q25.8 Other congenital malformations of great arteries	0.005	0.995	0.000
Q25.5 Atresia of pulmonary artery	0.005	0.995	0.000
Q25.2 Atresia of aorta	0.005	0.995	0.000
E22 Hyperfunction of pituitary gland	0.000	0.995	0.005
E64 Sequelae of malnutrition and other nutritional deficiencies	0.000	0.995	0.005
E63 Other nutritional deficiencies	0.000	0.995	0.005
E50 Vitamin A deficiency	0.000	0.995	0.005
E60 Dietary zinc deficiency	0.000	0.995	0.005
E59 Dietary selenium deficiency	0.000	0.995	0.005
E54 Ascorbic acid deficiency	0.000	0.995	0.005
E52 Niacin deficiency [pellagra]	0.000	0.995	0.005
Q54 Hypospadias	0.005	0.995	0.000
Q60.2 Renal agenesis, unspecified	0.005	0.995	0.000
Q62.2 Congenital megaloureter	0.005	0.995	0.000
Q07.0 Arnold-Chiari syndrome	0.005	0.995	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.005	0.995	0.000
Q13 Congenital malformations of anterior segment of eye	0.005	0.995	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.005	0.995	0.000
E23.7 Disorder of pituitary gland, unspecified	0.000	0.995	0.005
Q52.1 Doubling of vagina	0.005	0.995	0.000
E32 Diseases of thymus	0.000	0.995	0.005
E29 Testicular dysfunction	0.000	0.995	0.005
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.005	0.995	0.000
Q03.9 Congenital hydrocephalus, unspecified	0.005	0.995	0.000
Q03.8 Other congenital hydrocephalus	0.005	0.995	0.000
Q03.1 Atresia of foramina of Magendie and Luschka	0.005	0.995	0.000
Q14.1 Congenital malformation of retina	0.005	0.995	0.000
Q25.0 Patent ductus arteriosus	0.005	0.995	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.005	0.995	0.000
Q61.0 Congenital single renal cyst	0.005	0.995	0.000
Q34 Other congenital malformations of respiratory system	0.005	0.995	0.000
Q33 Congenital malformations of lung	0.005	0.995	0.000
Q32 Congenital malformations of trachea and bronchus	0.005	0.995	0.000
Q07.9 Congenital malformation of nervous system, unspecified	0.005	0.995	0.000
Q07.8 Other specified congenital malformations of nervous system	0.005	0.995	0.000
Q30 Congenital malformations of nose	0.005	0.995	0.000
E23.0 Hypopituitarism	0.000	0.995	0.005
Q62.8 Other congenital malformations of ureter	0.004	0.995	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.004	0.995	0.000
Q62.6 Malposition of ureter	0.004	0.995	0.000
Q62.4 Agenesis of ureter	0.004	0.995	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.004	0.995	0.000
Q62.1 Atresia and stenosis of ureter	0.004	0.995	0.000
Q62.0 Congenital hydronephrosis	0.004	0.995	0.000
Q31 Congenital malformations of larynx	0.005	0.995	0.000
E27.9 Disorder of adrenal gland, unspecified	0.000	0.995	0.005
Q00.2 Iniencephaly	0.004	0.995	0.000
Q00.1 Craniorachischisis	0.004	0.995	0.000
Q00.0 Anencephaly	0.004	0.995	0.000
Q01.9 Encephalocele, unspecified	0.004	0.995	0.000
Q01.8 Encephalocele of other sites	0.004	0.995	0.000
Q01.2 Occipital encephalocele	0.004	0.995	0.000
Q01.1 Nasofrontal encephalocele	0.004	0.995	0.000
Q01.0 Frontal encephalocele	0.004	0.995	0.000
Q06.9 Congenital malformation of spinal cord, unspecified	0.004	0.995	0.000
Q06.8 Other specified congenital malformations of spinal cord	0.004	0.995	0.000
Q06.4 Hydromyelia	0.004	0.995	0.000
Q06.3 Other congenital cauda equina malformations	0.004	0.995	0.000
Q06.2 Diastematomyelia	0.004	0.995	0.000
Q06.1 Hypoplasia and dysplasia of spinal cord	0.004	0.995	0.000
Q06.0 Amyelia	0.004	0.995	0.000
Q44.6 Cystic disease of liver	0.005	0.995	0.000
Q62.5 Duplication of ureter	0.004	0.995	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.004	0.995	0.000
Q15.0 Congenital glaucoma	0.004	0.995	0.000
Q89 Other congenital malformations, not elsewhere classified	0.004	0.995	0.000
M05.9 Seropositive rheumatoid arthritis, unspecified	0.004	0.996	0.000
Q54.9 Hypospadias, unspecified	0.004	0.996	0.000
Q40 Other congenital malformations of upper alimentary tract	0.004	0.996	0.000
Q53 Undescended testicle	0.004	0.996	0.000
Q25.1 Coarctation of aorta	0.004	0.996	0.000
Q91.7 Patau's syndrome, unspecified	0.004	0.996	0.000
Q91.6 Trisomy 13, translocation	0.004	0.996	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.004	0.996	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.004	0.996	0.000
Q91.3 Edwards' syndrome, unspecified	0.004	0.996	0.000
Q91.2 Trisomy 18, translocation	0.004	0.996	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.004	0.996	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.004	0.996	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.004	0.996	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.004	0.996	0.000
Q92.7 Triploidy and polyploidy	0.004	0.996	0.000
Q92.6 Extra marker chromosomes	0.004	0.996	0.000
Q92.5 Duplications with other complex rearrangements	0.004	0.996	0.000
Q92.4 Duplications seen only at prometaphase	0.004	0.996	0.000
Q92.3 Minor partial trisomy	0.004	0.996	0.000
Q92.2 Major partial trisomy	0.004	0.996	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.004	0.996	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.004	0.996	0.000
Q93.9 Deletion from autosomes, unspecified	0.004	0.996	0.000
Q93.8 Other deletions from the autosomes	0.004	0.996	0.000
Q93.7 Deletions with other complex rearrangements	0.004	0.996	0.000
Q93.6 Deletions seen only at prometaphase	0.004	0.996	0.000
Q93.5 Other deletions of part of a chromosome	0.004	0.996	0.000
Q93.4 Deletion of short arm of chromosome 5	0.004	0.996	0.000
Q93.3 Deletion of short arm of chromosome 4	0.004	0.996	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.004	0.996	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.004	0.996	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.004	0.996	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.004	0.996	0.000
Q95.8 Other balanced rearrangements and structural markers	0.004	0.996	0.000
Q95.5 Individuals with autosomal fragile site	0.004	0.996	0.000
Q95.4 Individuals with marker heterochromatin	0.004	0.996	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.004	0.996	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.004	0.996	0.000
Q95.1 Chromosome inversion in normal individual	0.004	0.996	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.004	0.996	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.004	0.996	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.004	0.996	0.000
Q97.3 Female with 46,XY karyotype	0.004	0.996	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.004	0.996	0.000
Q97.1 Female with more than three X chromosomes	0.004	0.996	0.000
Q97.0 Karyotype 47,XXX	0.004	0.996	0.000
Q25.6 Stenosis of pulmonary artery	0.004	0.996	0.000
Z43.4 Attention to other artificial openings of digestive tract	0.000	0.996	0.004
Q55 Other congenital malformations of male genital organs	0.004	0.996	0.000
Q36 Cleft lip	0.004	0.996	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.004	0.996	0.000
Q84 Other congenital malformations of integument	0.004	0.996	0.000
Q81 Epidermolysis bullosa	0.004	0.996	0.000
Q80 Congenital ichthyosis	0.004	0.996	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.004	0.996	0.000
Q90.2 Trisomy 21, translocation	0.004	0.996	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.004	0.996	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.004	0.996	0.000
E23.3 Hypothalamic dysfunction, not elsewhere classified	0.000	0.996	0.004
E23.1 Drug-induced hypopituitarism	0.000	0.996	0.004
Q25.4 Other congenital malformations of aorta	0.004	0.996	0.000
Q23.1 Congenital insufficiency of aortic valve	0.004	0.996	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.004	0.996	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.004	0.996	0.000
Q98.7 Male with sex chromosome mosaicism	0.004	0.996	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.004	0.996	0.000
Q98.5 Karyotype 47,XYY	0.004	0.996	0.000
Q98.3 Other male with 46,XX karyotype	0.004	0.996	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.004	0.996	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.004	0.996	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.004	0.996	0.000
E65-E68 Obesity and other hyperalimentation	0.000	0.996	0.004
Q21.0 Ventricular septal defect	0.004	0.996	0.000
Q87.4 Marfan's syndrome	0.004	0.996	0.000
Q12 Congenital lens malformations	0.004	0.996	0.000
E15-E16 Other disorders of glucose regulation and pancreatic internal secretion	0.000	0.996	0.004
E56.1 Deficiency of vitamin K	0.000	0.996	0.004
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.004	0.996	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.004	0.996	0.000
Q14.3 Congenital malformation of choroid	0.004	0.996	0.000
Q14.2 Congenital malformation of optic disk	0.004	0.996	0.000
Q14.0 Congenital malformation of vitreous humour	0.004	0.996	0.000
Q90.9 Down's syndrome, unspecified	0.004	0.996	0.000
Q37 Cleft palate with cleft lip	0.004	0.996	0.000
Q11.1 Other anophthalmos	0.004	0.996	0.000
Q54.1 Hypospadias, penile	0.004	0.996	0.000
Q21.3 Tetralogy of Fallot	0.004	0.996	0.000
Q52.5 Fusion of labia	0.004	0.996	0.000
Q21.4 Aortopulmonary septal defect	0.004	0.996	0.000
Q21.2 Atrioventricular septal defect	0.004	0.996	0.000
Q83 Congenital malformations of breast	0.004	0.996	0.000
E23.6 Other disorders of pituitary gland	0.000	0.996	0.004
Q44.4 Choledochal cyst	0.004	0.996	0.000
Q17.5 Prominent ear	0.004	0.996	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.004	0.996	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.004	0.996	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.004	0.996	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.004	0.996	0.000
E51.2 Wernicke's encephalopathy	0.000	0.996	0.004
Q15.9 Congenital malformation of eye, unspecified	0.004	0.996	0.000
Q15.8 Other specified congenital malformations of eye	0.004	0.996	0.000
Q52.9 Congenital malformation of female genitalia, unspecified	0.004	0.996	0.000
Q52.8 Other specified congenital malformations of female genitalia	0.004	0.996	0.000
Q52.7 Other congenital malformations of vulva	0.004	0.996	0.000
Q52.6 Congenital malformation of clitoris	0.004	0.996	0.000
Q52.4 Other congenital malformations of vagina	0.004	0.996	0.000
Q52.3 Imperforate hymen	0.004	0.996	0.000
Q52.2 Congenital rectovaginal fistula	0.004	0.996	0.000
Q52.0 Congenital absence of vagina	0.004	0.996	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.004	0.996	0.000
E61 Deficiency of other nutrient elements	0.000	0.996	0.004
Q35 Cleft palate	0.004	0.996	0.000
K91.3 Postoperative intestinal obstruction	0.001	0.996	0.003
Q44.5 Other congenital malformations of bile ducts	0.004	0.996	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.004	0.996	0.000
E20 Hypoparathyroidism	0.000	0.996	0.004
M05.97 Seropositive rheumatoid arthritis, unspecified (Ankle and foot)	0.004	0.996	0.000
E26 Hyperaldosteronism	0.000	0.996	0.004
E44 Protein-energy malnutrition of moderate and mild degree	0.000	0.996	0.004
E45 Retarded development following protein-energy malnutrition	0.000	0.996	0.004
E43 Unspecified severe protein-energy malnutrition	0.000	0.996	0.004
E42 Marasmic kwashiorkor	0.000	0.996	0.004
E41 Nutritional marasmus	0.000	0.996	0.004
E40 Kwashiorkor	0.000	0.996	0.004
E56.9 Vitamin deficiency, unspecified	0.000	0.996	0.004
E56.8 Deficiency of other vitamins	0.000	0.996	0.004
E56.0 Deficiency of vitamin E	0.000	0.996	0.004
Z43.6 Attention to other artificial openings of urinary tract	0.000	0.996	0.004
E30.9 Disorder of puberty, unspecified	0.000	0.996	0.004
E30.8 Other disorders of puberty	0.000	0.996	0.004
E30.1 Precocious puberty	0.000	0.996	0.004
E30.0 Delayed puberty	0.000	0.996	0.004
E31.9 Polyglandular dysfunction, unspecified	0.000	0.996	0.004
E31.8 Other polyglandular dysfunction	0.000	0.996	0.004
E31.1 Polyglandular hyperfunction	0.000	0.996	0.004

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