TreeWAS – Variant ID: rs5756506

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
D64.9 Anaemia, unspecified	0.000	0.314	0.686
D64 Other anaemias	0.000	0.492	0.508
D60-D64 Aplastic and other anaemias	0.000	0.571	0.429
D62 Acute posthaemorrhagic anaemia	0.000	0.573	0.427
D64.4 Congenital dyserythropoietic anaemia	0.000	0.635	0.364
D64.2 Secondary sideroblastic anaemia due to drugs and toxins	0.000	0.635	0.364
D64.1 Secondary sideroblastic anaemia due to disease	0.000	0.635	0.364
D64.0 Hereditary sideroblastic anaemia	0.000	0.635	0.364
D64.8 Other specified anaemias	0.000	0.649	0.351
D60 Acquired pure red cell aplasia [erythroblastopenia]	0.000	0.700	0.300
D64.3 Other sideroblastic anaemias	0.000	0.703	0.296
D61 Other aplastic anaemias	0.000	0.749	0.251
D60.8 Other acquired pure red cell aplasias	0.000	0.785	0.215
D60.1 Transient acquired pure red cell aplasia	0.000	0.785	0.215
D60.0 Chronic acquired pure red cell aplasia	0.000	0.785	0.215
D60.9 Acquired pure red cell aplasia, unspecified	0.000	0.793	0.207
D61.1 Drug-induced aplastic anaemia	0.000	0.803	0.197
D61.8 Other specified aplastic anaemias	0.000	0.820	0.180
D61.3 Idiopathic aplastic anaemia	0.000	0.820	0.180
D61.2 Aplastic anaemia due to other external agents	0.000	0.820	0.180
D61.0 Constitutional aplastic anaemia	0.000	0.822	0.177
D63 Anaemia in chronic diseases classified elsewhere	0.000	0.850	0.150
D63.1 Anaemia in other chronic diseases classified elsewhere	0.000	0.892	0.108
D61.9 Aplastic anaemia, unspecified	0.000	0.911	0.089
D63.0 Anaemia in neoplastic disease	0.000	0.941	0.059
D63.8 Anaemia in other chronic diseases classified elsewhere	0.000	0.943	0.057
E83.1 Disorders of iron metabolism	0.049	0.951	0.000
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.000	0.968	0.032
D50-D53 Nutritional anaemias	0.000	0.971	0.029
D50 Iron deficiency anaemia	0.000	0.974	0.026
D50.8 Other iron deficiency anaemias	0.000	0.976	0.024
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)	0.000	0.976	0.024
D51 Vitamin B12 deficiency anaemia	0.000	0.976	0.024
D53 Other nutritional anaemias	0.000	0.977	0.023
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency	0.000	0.977	0.023
D55-D59 Haemolytic anaemias	0.000	0.980	0.020
D52 Folate deficiency anaemia	0.000	0.981	0.019
D53.9 Nutritional anaemia, unspecified	0.000	0.981	0.019
D50.1 Sideropenic dysphagia	0.000	0.982	0.018
D51.8 Other vitamin B12 deficiency anaemias	0.000	0.982	0.017
D51.2 Transcobalamin II deficiency	0.000	0.982	0.017
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria	0.000	0.982	0.017
D51.3 Other dietary vitamin B12 deficiency anaemia	0.000	0.983	0.017
Q21.0 Ventricular septal defect	0.017	0.983	0.000
D53.8 Other specified nutritional anaemias	0.000	0.983	0.017
D53.2 Scorbutic anaemia	0.000	0.983	0.017
D53.1 Other megaloblastic anaemias, not elsewhere classified	0.000	0.983	0.017
D53.0 Protein deficiency anaemia	0.000	0.983	0.017
Q21 Congenital malformations of cardiac septa	0.016	0.984	0.000
Q24 Other congenital malformations of heart	0.016	0.984	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.016	0.984	0.000
Q60.0 Renal agenesis, unilateral	0.015	0.985	0.000
D57 Sickle-cell disorders	0.000	0.985	0.015
D55 Anaemia due to enzyme disorders	0.000	0.985	0.015
G55.2 Nerve root and plexus compressions in spondylosis	0.000	0.985	0.015
D58 Other hereditary haemolytic anaemias	0.000	0.985	0.014
Q24.8 Other specified congenital malformations of heart	0.014	0.986	0.000
D59 Acquired haemolytic anaemia	0.000	0.986	0.014
Q60 Renal agenesis and other reduction defects of kidney	0.014	0.986	0.000
Q21.8 Other congenital malformations of cardiac septa	0.014	0.986	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.014	0.986	0.000
D52.8 Other folate deficiency anaemias	0.000	0.986	0.014
D52.1 Drug-induced folate deficiency anaemia	0.000	0.986	0.014
D52.0 Dietary folate deficiency anaemia	0.000	0.986	0.014
F33.9 Recurrent depressive disorder, unspecified	0.000	0.987	0.013
D56 Thalassaemia	0.000	0.987	0.013
Q24.5 Malformation of coronary vessels	0.013	0.987	0.000
Q21.3 Tetralogy of Fallot	0.013	0.987	0.000
Q27 Other congenital malformations of peripheral vascular system	0.013	0.987	0.000
Q24.0 Dextrocardia	0.012	0.987	0.000
E83 Disorders of mineral metabolism	0.012	0.988	0.000
Q60-Q64 Congenital malformations of the urinary system	0.012	0.988	0.000
D59.1 Other autoimmune haemolytic anaemias	0.000	0.988	0.012
Q60.2 Renal agenesis, unspecified	0.012	0.988	0.000
Q21.4 Aortopulmonary septal defect	0.012	0.988	0.000
Q21.2 Atrioventricular septal defect	0.012	0.988	0.000
D51.9 Vitamin B12 deficiency anaemia, unspecified	0.000	0.988	0.012
Q25 Congenital malformations of great arteries	0.012	0.988	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.012	0.988	0.000
Q24.6 Congenital heart block	0.012	0.988	0.000
Q24.4 Congenital subaortic stenosis	0.012	0.988	0.000
Q24.3 Pulmonary infundibular stenosis	0.012	0.988	0.000
Q24.2 Cor triatriatum	0.012	0.988	0.000
Q24.1 Levocardia	0.012	0.988	0.000
F33.1 Recurrent depressive disorder, current episode moderate	0.000	0.988	0.012
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.012	0.988	0.000
Q26 Congenital malformations of great veins	0.011	0.989	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.011	0.989	0.000
F33 Recurrent depressive disorder	0.000	0.989	0.011
D52.9 Folate deficiency anaemia, unspecified	0.000	0.989	0.011
D58.0 Hereditary spherocytosis	0.000	0.989	0.011
D55.9 Anaemia due to enzyme disorder, unspecified	0.000	0.989	0.011
D55.8 Other anaemias due to enzyme disorders	0.000	0.989	0.011
D55.3 Anaemia due to disorders of nucleotide metabolism	0.000	0.989	0.011
D55.2 Anaemia due to disorders of glycolytic enzymes	0.000	0.989	0.011
D55.1 Anaemia due to other disorders of glutathione metabolism	0.000	0.989	0.011
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency	0.000	0.989	0.011
D57.8 Other sickle-cell disorders	0.000	0.989	0.011
D57.3 Sickle-cell trait	0.000	0.989	0.011
D57.2 Double heterozygous sickling disorders	0.000	0.989	0.011
D57.1 Sickle-cell anaemia without crisis	0.000	0.989	0.011
D57.0 Sickle-cell anaemia with crisis	0.000	0.989	0.011
D58.8 Other specified hereditary haemolytic anaemias	0.000	0.989	0.010
D58.1 Hereditary elliptocytosis	0.000	0.989	0.010
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.011	0.989	0.000
Q80-Q89 Other congenital malformations	0.011	0.989	0.000
D59.8 Other acquired haemolytic anaemias	0.000	0.989	0.010
D59.6 Haemoglobinuria due to haemolysis from other external causes	0.000	0.989	0.010
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]	0.000	0.989	0.010
D59.4 Other nonautoimmune haemolytic anaemias	0.000	0.989	0.010
D59.3 Haemolytic-uraemic syndrome	0.000	0.989	0.010
D59.2 Drug-induced nonautoimmune haemolytic anaemia	0.000	0.989	0.010
Q21.9 Congenital malformation of cardiac septum, unspecified	0.010	0.990	0.000
Q60.6 Potter's syndrome	0.010	0.990	0.000
Q60.5 Renal hypoplasia, unspecified	0.010	0.990	0.000
Q60.4 Renal hypoplasia, bilateral	0.010	0.990	0.000
Q60.3 Renal hypoplasia, unilateral	0.010	0.990	0.000
Q60.1 Renal agenesis, bilateral	0.010	0.990	0.000
Q21.1 Atrial septal defect	0.010	0.990	0.000
D58.2 Other haemoglobinopathies	0.000	0.990	0.010
Q82 Other congenital malformations of skin	0.010	0.990	0.000
D58.9 Hereditary haemolytic anaemia, unspecified	0.000	0.990	0.010
Q27.8 Other specified congenital malformations of peripheral vascular system	0.010	0.990	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.010	0.990	0.000
D56.9 Thalassaemia, unspecified	0.000	0.990	0.010
D56.8 Other thalassaemias	0.000	0.990	0.010
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]	0.000	0.990	0.010
D56.2 Delta-beta thalassaemia	0.000	0.990	0.010
D56.0 Alpha thalassaemia	0.000	0.990	0.010
D59.0 Drug-induced autoimmune haemolytic anaemia	0.000	0.990	0.010
E83.9 Disorder of mineral metabolism, unspecified	0.010	0.990	0.000
D70-D77 Other diseases of blood and blood-forming organs	0.000	0.990	0.010
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.010	0.990	0.000
D56.1 Beta thalassaemia	0.000	0.990	0.009
Q27.4 Congenital phlebectasia	0.009	0.990	0.000
Q27.2 Other congenital malformations of renal artery	0.009	0.990	0.000
Q27.1 Congenital renal artery stenosis	0.009	0.990	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.009	0.990	0.000
Q28 Other congenital malformations of circulatory system	0.009	0.990	0.000
Q27.3 Peripheral arteriovenous malformation	0.009	0.991	0.000
Q82.0 Hereditary lymphoedema	0.009	0.991	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.009	0.991	0.000
F33.2 Recurrent depressive disorder, current episode severe without psychotic symptoms	0.000	0.991	0.009
E83.8 Other disorders of mineral metabolism	0.009	0.991	0.000
E83.2 Disorders of zinc metabolism	0.009	0.991	0.000
E83.0 Disorders of copper metabolism	0.009	0.991	0.000
Q22.5 Ebstein's anomaly	0.009	0.991	0.000
Q82.8 Other specified congenital malformations of skin	0.009	0.991	0.000
F33.3 Recurrent depressive disorder, current episode severe with psychotic symptoms	0.000	0.991	0.009
O68.0 Labour and delivery complicated by foetal heart rate anomaly	0.000	0.991	0.009
Q25.0 Patent ductus arteriosus	0.009	0.991	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.009	0.991	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.009	0.991	0.000
Q25.8 Other congenital malformations of great arteries	0.009	0.991	0.000
Q25.6 Stenosis of pulmonary artery	0.009	0.991	0.000
Q25.5 Atresia of pulmonary artery	0.009	0.991	0.000
Q25.2 Atresia of aorta	0.009	0.991	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.008	0.991	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.008	0.991	0.000
Q22.6 Hypoplastic right heart syndrome	0.008	0.991	0.000
Q22.4 Congenital tricuspid stenosis	0.008	0.991	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.008	0.991	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.008	0.991	0.000
Q22.0 Pulmonary valve atresia	0.008	0.991	0.000
Q63 Other congenital malformations of kidney	0.009	0.991	0.000
K50.0 Crohn's disease of small intestine	0.009	0.991	0.000
Q64 Other congenital malformations of urinary system	0.009	0.991	0.000
Q22.1 Congenital pulmonary valve stenosis	0.008	0.991	0.000
D56.3 Thalassaemia trait	0.000	0.991	0.008
Q63.2 Ectopic kidney	0.008	0.991	0.000
Q25.3 Stenosis of aorta	0.008	0.991	0.000
D75 Other diseases of blood and blood-forming organs	0.000	0.991	0.008
Q35-Q37 Cleft lip and cleft palate	0.008	0.992	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.008	0.992	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.008	0.992	0.000
Q20.6 Isomerism of atrial appendages	0.008	0.992	0.000
Q20.5 Discordant atrioventricular connexion	0.008	0.992	0.000
Q20.4 Double inlet ventricle	0.008	0.992	0.000
Q20.3 Discordant ventriculoarterial connexion	0.008	0.992	0.000
Q20.2 Double outlet left ventricle	0.008	0.992	0.000
Q20.1 Double outlet right ventricle	0.008	0.992	0.000
Q20.0 Common arterial trunk	0.008	0.992	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.008	0.992	0.000
Q26.8 Other congenital malformations of great veins	0.008	0.992	0.000
Q26.6 Portal vein-hepatic artery fistula	0.008	0.992	0.000
Q26.5 Anomalous portal venous connexion	0.008	0.992	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.008	0.992	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.008	0.992	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.008	0.992	0.000
Q26.1 Persistent left superior vena cava	0.008	0.992	0.000
Q26.0 Congenital stenosis of vena cava	0.008	0.992	0.000
E83.3 Disorders of phosphorus metabolism	0.008	0.992	0.000
F33.8 Other recurrent depressive disorders	0.000	0.992	0.008
Q25.4 Other congenital malformations of aorta	0.008	0.992	0.000
Q85 Phakomatoses, not elsewhere classified	0.008	0.992	0.000
D59.9 Acquired haemolytic anaemia, unspecified	0.000	0.992	0.008
M47.26 Other spondylosis with radiculopathy (Lumbar region)	0.000	0.992	0.008
Q38-Q45 Other congenital malformations of the digestive system	0.008	0.992	0.000
Q25.1 Coarctation of aorta	0.008	0.992	0.000
Q00-Q07 Congenital malformations of the nervous system	0.008	0.992	0.000
Q89 Other congenital malformations, not elsewhere classified	0.008	0.992	0.000
F33.4 Recurrent depressive disorder, currently in remission	0.000	0.992	0.008
Q62.5 Duplication of ureter	0.008	0.992	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.008	0.992	0.000
Q84 Other congenital malformations of integument	0.008	0.992	0.000
Q81 Epidermolysis bullosa	0.008	0.992	0.000
Q80 Congenital ichthyosis	0.008	0.992	0.000
Q30 Congenital malformations of nose	0.008	0.992	0.000
Z73.3 Stress, not elsewhere classified	0.000	0.992	0.008
D75.9 Disease of blood and blood-forming organs, unspecified	0.000	0.992	0.008
Q82.2 Mastocytosis	0.008	0.992	0.000
Q40 Other congenital malformations of upper alimentary tract	0.008	0.992	0.000
Q82.9 Congenital malformation of skin, unspecified	0.007	0.992	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.007	0.992	0.000
Q82.3 Incontinentia pigmenti	0.007	0.992	0.000
Q82.1 Xeroderma pigmentosum	0.007	0.992	0.000
Q96 Turner's syndrome	0.007	0.992	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.007	0.992	0.000
Q61 Cystic kidney disease	0.007	0.993	0.000
Q50-Q56 Congenital malformations of genital organs	0.007	0.993	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.007	0.993	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.007	0.993	0.000
D74 Methaemoglobinaemia	0.000	0.993	0.007
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere	0.000	0.993	0.007
D71 Functional disorders of polymorphonuclear neutrophils	0.000	0.993	0.007
Q62.8 Other congenital malformations of ureter	0.007	0.993	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.007	0.993	0.000
Q62.6 Malposition of ureter	0.007	0.993	0.000
Q62.4 Agenesis of ureter	0.007	0.993	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.007	0.993	0.000
Q62.2 Congenital megaloureter	0.007	0.993	0.000
Q62.1 Atresia and stenosis of ureter	0.007	0.993	0.000
Q62.0 Congenital hydronephrosis	0.007	0.993	0.000
D75.1 Secondary polycythaemia	0.000	0.993	0.007
Q23 Congenital malformations of aortic and mitral valves	0.007	0.993	0.000
Q40.2 Other specified congenital malformations of stomach	0.007	0.993	0.000
E83.4 Disorders of magnesium metabolism	0.007	0.993	0.000
Q83 Congenital malformations of breast	0.007	0.993	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.007	0.993	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.007	0.993	0.000
Q28.1 Other malformations of precerebral vessels	0.007	0.993	0.000
Q85.9 Phakomatosis, unspecified	0.007	0.993	0.000
Q31 Congenital malformations of larynx	0.007	0.993	0.000
T81.3 Disruption of operation wound, not elsewhere classified	0.007	0.993	0.000
Q34 Other congenital malformations of respiratory system	0.007	0.993	0.000
Q33 Congenital malformations of lung	0.007	0.993	0.000
Q32 Congenital malformations of trachea and bronchus	0.007	0.993	0.000
Q28.3 Other malformations of cerebral vessels	0.007	0.993	0.000
Q82.5 Congenital nonneoplastic naevus	0.007	0.993	0.000
Z35.0 Supervision of pregnancy with history of infertility	0.000	0.993	0.007
Z36.4 Antenatal screening for foetal growth retardation using ultrasound and other physical methods	0.000	0.993	0.007
M70.22 Olecranon bursitis-Upper arm	0.007	0.993	0.000
Q96.9 Turner's syndrome, unspecified	0.007	0.993	0.000
Q30.3 Congenital perforated nasal septum	0.007	0.993	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.006	0.993	0.000
Z36.3 Antenatal screening for malformations using ultrasound and other physical methods	0.000	0.993	0.007
Q07 Other congenital malformations of nervous system	0.006	0.993	0.000
Q12 Congenital lens malformations	0.006	0.993	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.006	0.993	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.006	0.993	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.006	0.993	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.006	0.993	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.006	0.993	0.000
E83.5 Disorders of calcium metabolism	0.007	0.993	0.000
F33.0 Recurrent depressive disorder, current episode mild	0.000	0.993	0.006
Q63.9 Congenital malformation of kidney, unspecified	0.006	0.993	0.000
Q63.8 Other specified congenital malformations of kidney	0.006	0.993	0.000
Q63.3 Hyperplastic and giant kidney	0.006	0.993	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.006	0.994	0.000
Q64.8 Other specified congenital malformations of urinary system	0.006	0.994	0.000
Q64.6 Congenital diverticulum of bladder	0.006	0.994	0.000
Q64.5 Congenital absence of bladder and urethra	0.006	0.994	0.000
Q64.4 Malformation of urachus	0.006	0.994	0.000
Q64.2 Congenital posterior urethral valves	0.006	0.994	0.000
Q64.1 Exstrophy of urinary bladder	0.006	0.994	0.000
Q64.0 Epispadias	0.006	0.994	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.006	0.994	0.000
D75.0 Familial erythrocytosis	0.000	0.994	0.006
Q35 Cleft palate	0.006	0.994	0.000
Q36 Cleft lip	0.006	0.994	0.000
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system	0.000	0.994	0.006
K50 Crohn's disease [regional enteritis]	0.006	0.994	0.000
Q06 Other congenital malformations of spinal cord	0.006	0.994	0.000
Q39 Congenital malformations of oesophagus	0.006	0.994	0.000
K50.1 Crohn's disease of large intestine	0.006	0.994	0.000
Q85.1 Tuberous sclerosis	0.006	0.994	0.000
Q90 Down's syndrome	0.006	0.994	0.000
Z35 Supervision of high-risk pregnancy	0.000	0.994	0.006
D73 Diseases of spleen	0.000	0.994	0.006
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.006	0.994	0.000
Q03 Congenital hydrocephalus	0.006	0.994	0.000
E80.4 Gilbert's syndrome	0.006	0.994	0.000
Q89.2 Congenital malformations of other endocrine glands	0.006	0.994	0.000
Q37 Cleft palate with cleft lip	0.006	0.994	0.000
Q61.3 Polycystic kidney, unspecified	0.006	0.994	0.000
Z36 Antenatal screening	0.000	0.994	0.006
Q12.0 Congenital cataract	0.006	0.994	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.006	0.994	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.006	0.994	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.006	0.994	0.000
D75.8 Other specified diseases of blood and blood-forming organs	0.000	0.994	0.006
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
Q40.3 Congenital malformation of stomach, unspecified	0.006	0.994	0.000
Q89.9 Congenital malformation, unspecified	0.006	0.994	0.000
Q89.8 Other specified congenital malformations	0.006	0.994	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.006	0.994	0.000
Q89.4 Conjoined twins	0.006	0.994	0.000
Q89.3 Situs inversus	0.006	0.994	0.000
Q89.1 Congenital malformations of adrenal gland	0.006	0.994	0.000
Q89.0 Congenital malformations of spleen	0.006	0.994	0.000
Q61.4 Renal dysplasia	0.006	0.994	0.000
Z36.0 Antenatal screening for chromosomal anomalies	0.000	0.994	0.006
Q85.0 Neurofibromatosis (nonmalignant)	0.006	0.994	0.000
Q80.9 Congenital ichthyosis, unspecified	0.006	0.994	0.000
Q80.8 Other congenital ichthyosis	0.006	0.994	0.000
Q80.4 Harlequin foetus	0.006	0.994	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.006	0.994	0.000
Q80.2 Lamellar ichthyosis	0.006	0.994	0.000
Q80.1 X-linked ichthyosis	0.006	0.994	0.000
Q80.0 Ichthyosis vulgaris	0.006	0.994	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.006	0.994	0.000
Q81.8 Other epidermolysis bullosa	0.006	0.994	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.006	0.994	0.000
Q81.1 Epidermolysis bullosa letalis	0.006	0.994	0.000
Q81.0 Epidermolysis bullosa simplex	0.006	0.994	0.000
Q84.9 Congenital malformation of integument, unspecified	0.006	0.994	0.000
Q84.8 Other specified congenital malformations of integument	0.006	0.994	0.000
Q84.6 Other congenital malformations of nails	0.006	0.994	0.000
Q84.5 Enlarged and hypertrophic nails	0.006	0.994	0.000
Q84.4 Congenital leukonychia	0.006	0.994	0.000
Q84.3 Anonychia	0.006	0.994	0.000
Q84.2 Other congenital malformations of hair	0.006	0.994	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.006	0.994	0.000
Q84.0 Congenital alopecia	0.006	0.994	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.006	0.994	0.000
Q86.2 Dysmorphism due to warfarin	0.006	0.994	0.000
Q86.1 Foetal hydantoin syndrome	0.006	0.994	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.006	0.994	0.000
Q04 Other congenital malformations of brain	0.006	0.994	0.000
Z35.8 Supervision of other high-risk pregnancies	0.000	0.994	0.006
Q52 Other congenital malformations of female genitalia	0.006	0.994	0.000
Q61.5 Medullary cystic kidney	0.006	0.994	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.006	0.994	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.006	0.994	0.000
Q30.9 Congenital malformation of nose, unspecified	0.006	0.994	0.000
Q30.8 Other congenital malformations of nose	0.006	0.994	0.000
Q30.2 Fissured, notched and cleft nose	0.006	0.994	0.000
Q30.1 Agenesis and underdevelopment of nose	0.006	0.994	0.000
Q30.0 Choanal atresia	0.006	0.994	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.006	0.994	0.000
D80-D89 Certain disorders involving the immune mechanism	0.000	0.994	0.006
Q54 Hypospadias	0.006	0.994	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.006	0.994	0.000
Q45 Other congenital malformations of digestive system	0.006	0.994	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.006	0.994	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.006	0.994	0.000
Q40.1 Congenital hiatus hernia	0.006	0.994	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.006	0.994	0.000
Q53 Undescended testicle	0.006	0.994	0.000
Q96.8 Other variants of Turner's syndrome	0.005	0.994	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.005	0.994	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.005	0.994	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.005	0.994	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.005	0.994	0.000
Q96.0 Karyotype 45,X	0.005	0.994	0.000
Q61.8 Other cystic kidney diseases	0.006	0.994	0.000
Q61.1 Polycystic kidney, infantile type	0.006	0.994	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.005	0.994	0.000
Q55 Other congenital malformations of male genital organs	0.005	0.994	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.005	0.994	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.005	0.994	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.005	0.994	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.005	0.994	0.000
Q13 Congenital malformations of anterior segment of eye	0.005	0.994	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.005	0.994	0.000
D74.9 Methaemoglobinaemia, unspecified	0.000	0.994	0.005
D74.8 Other methaemoglobinaemias	0.000	0.994	0.005
D74.0 Congenital methaemoglobinaemia	0.000	0.994	0.005
Q61.9 Cystic kidney disease, unspecified	0.005	0.994	0.000
Q14 Congenital malformations of posterior segment of eye	0.005	0.994	0.000
Q23.3 Congenital mitral insufficiency	0.005	0.995	0.000
Q83.8 Other congenital malformations of breast	0.005	0.995	0.000
Z35.2 Supervision of pregnancy with other poor reproductive or obstetric history	0.000	0.995	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
Q07.0 Arnold-Chiari syndrome	0.005	0.995	0.000
Q83.9 Congenital malformation of breast, unspecified	0.005	0.995	0.000
Q83.3 Accessory nipple	0.005	0.995	0.000
Q83.2 Absent nipple	0.005	0.995	0.000
Q83.0 Congenital absence of breast with absent nipple	0.005	0.995	0.000
D72 Other disorders of white blood cells	0.000	0.995	0.005
Q31.0 Web of larynx	0.005	0.995	0.000
Z35.4 Supervision of pregnancy with grand multiparity	0.000	0.995	0.005
D73.3 Abscess of spleen	0.000	0.995	0.005
Q31.9 Congenital malformation of larynx, unspecified	0.005	0.995	0.000
Q31.8 Other congenital malformations of larynx	0.005	0.995	0.000
Q31.5 Congenital laryngomalacia	0.005	0.995	0.000
Q31.4 Congenital laryngeal stridor	0.005	0.995	0.000
Q31.3 Laryngocele	0.005	0.995	0.000
Q31.2 Laryngeal hypoplasia	0.005	0.995	0.000
Q31.1 Congenital subglottic stenosis	0.005	0.995	0.000
Q32.4 Other congenital malformations of bronchus	0.005	0.995	0.000
Q32.3 Congenital stenosis of bronchus	0.005	0.995	0.000
Q32.2 Congenital bronchomalacia	0.005	0.995	0.000
Q32.1 Other congenital malformations of trachea	0.005	0.995	0.000
Q32.0 Congenital tracheomalacia	0.005	0.995	0.000
Q33.9 Congenital malformation of lung, unspecified	0.005	0.995	0.000
Q33.8 Other congenital malformations of lung	0.005	0.995	0.000
Q33.6 Hypoplasia and dysplasia of lung	0.005	0.995	0.000
Q33.5 Ectopic tissue in lung	0.005	0.995	0.000
Q33.4 Congenital bronchiectasis	0.005	0.995	0.000
Q33.3 Agenesis of lung	0.005	0.995	0.000
Q33.2 Sequestration of lung	0.005	0.995	0.000
Q33.1 Accessory lobe of lung	0.005	0.995	0.000
Q33.0 Congenital cystic lung	0.005	0.995	0.000
Q34.9 Congenital malformation of respiratory system, unspecified	0.005	0.995	0.000
Q34.8 Other specified congenital malformations of respiratory system	0.005	0.995	0.000
Q34.1 Congenital cyst of mediastinum	0.005	0.995	0.000
Q34.0 Anomaly of pleura	0.005	0.995	0.000
M79.00 Rheumatism, unspecified (Multiple sites)	0.000	0.995	0.005
Q39.6 Diverticulum of oesophagus	0.005	0.995	0.000
Q54.1 Hypospadias, penile	0.005	0.995	0.000
Q07.8 Other specified congenital malformations of nervous system	0.005	0.995	0.000
Q51 Congenital malformations of uterus and cervix	0.005	0.995	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.005	0.995	0.000
Q15 Other congenital malformations of eye	0.005	0.995	0.000
Q38.0 Congenital malformations of lips, not elsewhere classified	0.005	0.995	0.000
D73.0 Hyposplenism	0.000	0.995	0.005
Q06.8 Other specified congenital malformations of spinal cord	0.005	0.995	0.000
D75.2 Essential thrombocytosis	0.000	0.995	0.005
Q35.9 Cleft palate, unspecified	0.005	0.995	0.000
Q07.9 Congenital malformation of nervous system, unspecified	0.005	0.995	0.000
Q12.9 Congenital lens malformation, unspecified	0.005	0.995	0.000
Q12.8 Other congenital lens malformations	0.005	0.995	0.000
Q12.4 Spherophakia	0.005	0.995	0.000
Q12.3 Congenital aphakia	0.005	0.995	0.000
Q12.2 Coloboma of lens	0.005	0.995	0.000
Q12.1 Congenital displaced lens	0.005	0.995	0.000
Q91.7 Patau's syndrome, unspecified	0.005	0.995	0.000
Q91.6 Trisomy 13, translocation	0.005	0.995	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.005	0.995	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.005	0.995	0.000
Q91.3 Edwards' syndrome, unspecified	0.005	0.995	0.000
Q91.2 Trisomy 18, translocation	0.005	0.995	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.005	0.995	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.005	0.995	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.005	0.995	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.005	0.995	0.000
Q92.7 Triploidy and polyploidy	0.005	0.995	0.000
Q92.6 Extra marker chromosomes	0.005	0.995	0.000
Q92.5 Duplications with other complex rearrangements	0.005	0.995	0.000
Q92.4 Duplications seen only at prometaphase	0.005	0.995	0.000
Q92.3 Minor partial trisomy	0.005	0.995	0.000
Q92.2 Major partial trisomy	0.005	0.995	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.005	0.995	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.005	0.995	0.000
Q93.9 Deletion from autosomes, unspecified	0.005	0.995	0.000
Q93.8 Other deletions from the autosomes	0.005	0.995	0.000
Q93.7 Deletions with other complex rearrangements	0.005	0.995	0.000
Q93.6 Deletions seen only at prometaphase	0.005	0.995	0.000
Q93.5 Other deletions of part of a chromosome	0.005	0.995	0.000
Q93.4 Deletion of short arm of chromosome 5	0.005	0.995	0.000
Q93.3 Deletion of short arm of chromosome 4	0.005	0.995	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.005	0.995	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.005	0.995	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.005	0.995	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.005	0.995	0.000
Q95.8 Other balanced rearrangements and structural markers	0.005	0.995	0.000
Q95.5 Individuals with autosomal fragile site	0.005	0.995	0.000
Q95.4 Individuals with marker heterochromatin	0.005	0.995	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.005	0.995	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.005	0.995	0.000
Q95.1 Chromosome inversion in normal individual	0.005	0.995	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.005	0.995	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.005	0.995	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.005	0.995	0.000
Q97.3 Female with 46,XY karyotype	0.005	0.995	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.005	0.995	0.000
Q97.1 Female with more than three X chromosomes	0.005	0.995	0.000
Q97.0 Karyotype 47,XXX	0.005	0.995	0.000
Z35.1 Supervision of pregnancy with history of abortive outcome	0.000	0.995	0.005
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.005	0.995	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.005	0.995	0.000
Q17 Other congenital malformations of ear	0.005	0.995	0.000
Q04.8 Other specified congenital malformations of brain	0.005	0.995	0.000
Q35.8 (Cleft palate, unspecified, bilateral)	0.005	0.995	0.000
Q35.7 Cleft uvula	0.005	0.995	0.000
Q35.6 Cleft palate, medial	0.005	0.995	0.000
Q35.5 Cleft hard palate with cleft soft palate	0.005	0.995	0.000
Q35.4 (Cleft hard palate with cleft soft palate, bilateral)	0.005	0.995	0.000
Q35.3 Cleft soft palate	0.005	0.995	0.000
Q35.2 (Cleft soft palate, bilateral)	0.005	0.995	0.000
Q35.1 Cleft hard palate	0.005	0.995	0.000
Q35.0 (Cleft hard palate, bilateral)	0.005	0.995	0.000
Q52.1 Doubling of vagina	0.005	0.995	0.000
Q99.9 Chromosomal abnormality, unspecified	0.005	0.995	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