TreeWAS – Variant ID: rs1412337

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
N95.2 Postmenopausal atrophic vaginitis	0.000	0.953	0.047
E28.2 Polycystic ovarian syndrome	0.026	0.974	0.000
E28 Ovarian dysfunction	0.026	0.974	0.000
E20-E35 Disorders of other endocrine glands	0.026	0.974	0.000
R19.5 Other fecal abnormalities	0.025	0.975	0.000
E27 Other disorders of adrenal gland	0.024	0.976	0.000
E23 Hypofunction and other disorders of pituitary gland	0.024	0.976	0.000
E24 Cushing's syndrome	0.024	0.976	0.000
E27.9 Disorder of adrenal gland, unspecified	0.023	0.977	0.000
E27.8 Other specified disorders of adrenal gland	0.022	0.978	0.000
E23.0 Hypopituitarism	0.022	0.978	0.000
E28.3 Primary ovarian failure	0.022	0.978	0.000
N95 Menopausal and other perimenopausal disorders	0.000	0.979	0.021
E27.2 Addisonian crisis	0.021	0.979	0.000
E20 Hypoparathyroidism	0.021	0.979	0.000
N95.3 States associated with artificial menopause	0.000	0.979	0.021
E34 Other endocrine disorders	0.021	0.979	0.000
E24.0 Pituitary-dependent Cushing's disease	0.020	0.980	0.000
E29 Testicular dysfunction	0.020	0.980	0.000
N95.9 Menopausal and perimenopausal disorder, unspecified	0.000	0.981	0.019
E24.2 Drug-induced Cushing's syndrome	0.019	0.981	0.000
E28.9 Ovarian dysfunction, unspecified	0.019	0.981	0.000
E28.8 Other ovarian dysfunction	0.019	0.981	0.000
E28.1 Androgen excess	0.019	0.981	0.000
E28.0 Oestrogen excess	0.019	0.981	0.000
E24.9 Cushing's syndrome, unspecified	0.019	0.981	0.000
E23.7 Disorder of pituitary gland, unspecified	0.019	0.981	0.000
E35 Disorders of endocrine glands in diseases classified elsewhere	0.019	0.981	0.000
E32 Diseases of thymus	0.019	0.981	0.000
E31 Polyglandular dysfunction	0.019	0.981	0.000
E30 Disorders of puberty, not elsewhere classified	0.019	0.981	0.000
E25 Adrenogenital disorders	0.019	0.981	0.000
R63.0 Anorexia	0.000	0.982	0.018
E20.9 Hypoparathyroidism, unspecified	0.018	0.982	0.000
E26 Hyperaldosteronism	0.018	0.982	0.000
E27.5 Adrenomedullary hyperfunction	0.018	0.982	0.000
E27.0 Other adrenocortical overactivity	0.018	0.982	0.000
E23.2 Diabetes insipidus	0.018	0.982	0.000
E23.3 Hypothalamic dysfunction, not elsewhere classified	0.017	0.983	0.000
E23.1 Drug-induced hypopituitarism	0.017	0.983	0.000
E23.6 Other disorders of pituitary gland	0.017	0.983	0.000
E24.8 Other Cushing's syndrome	0.017	0.983	0.000
E24.4 Alcohol-induced pseudo-Cushing's syndrome	0.017	0.983	0.000
E24.3 Ectopic ACTH syndrome	0.017	0.983	0.000
E24.1 Nelson's syndrome	0.017	0.983	0.000
E34.9 Endocrine disorder, unspecified	0.017	0.983	0.000
E27.3 Drug-induced adrenocortical insufficiency	0.017	0.983	0.000
E22 Hyperfunction of pituitary gland	0.016	0.984	0.000
E29.1 Testicular hypofunction	0.016	0.984	0.000
E20.8 Other hypoparathyroidism	0.015	0.984	0.000
E20.1 Pseudohypoparathyroidism	0.015	0.984	0.000
E20.0 Idiopathic hypoparathyroidism	0.015	0.984	0.000
E34.0 Carcinoid syndrome	0.015	0.984	0.000
E34.5 Androgen resistance syndrome	0.015	0.985	0.000
E34.4 Constitutional tall stature	0.015	0.985	0.000
E34.3 Short stature, not elsewhere classified	0.015	0.985	0.000
E34.2 Ectopic hormone secretion, not elsewhere classified	0.015	0.985	0.000
E34.1 Other hypersecretion of intestinal hormones	0.015	0.985	0.000
E29.9 Testicular dysfunction, unspecified	0.014	0.985	0.000
E29.8 Other testicular dysfunction	0.014	0.985	0.000
E29.0 Testicular hyperfunction	0.014	0.985	0.000
Z90.7 Acquired absence of genital organ(s)	0.014	0.986	0.000
E27.4 Other and unspecified adrenocortical insufficiency	0.014	0.986	0.000
E34.8 Other specified endocrine disorders	0.014	0.986	0.000
E25.9 Adrenogenital disorder, unspecified	0.014	0.986	0.000
E25.8 Other adrenogenital disorders	0.014	0.986	0.000
E25.0 Congenital adrenogenital disorders associated with enzyme deficiency	0.014	0.986	0.000
E30.9 Disorder of puberty, unspecified	0.014	0.986	0.000
E30.8 Other disorders of puberty	0.014	0.986	0.000
E30.1 Precocious puberty	0.014	0.986	0.000
E30.0 Delayed puberty	0.014	0.986	0.000
E31.9 Polyglandular dysfunction, unspecified	0.014	0.986	0.000
E31.8 Other polyglandular dysfunction	0.014	0.986	0.000
E31.1 Polyglandular hyperfunction	0.014	0.986	0.000
E31.0 Autoimmune polyglandular failure	0.014	0.986	0.000
E32.9 Disease of thymus, unspecified	0.014	0.986	0.000
E32.8 Other diseases of thymus	0.014	0.986	0.000
E32.1 Abscess of thymus	0.014	0.986	0.000
E32.0 Persistent hyperplasia of thymus	0.014	0.986	0.000
E35.8 Disorders of other endocrine glands in diseases classified elsewhere	0.014	0.986	0.000
E35.1 Disorders of adrenal glands in diseases classified elsewhere	0.014	0.986	0.000
E35.0 Disorders of thyroid gland in diseases classified elsewhere	0.014	0.986	0.000
E26.9 Hyperaldosteronism, unspecified	0.013	0.987	0.000
E26.8 Other hyperaldosteronism	0.013	0.987	0.000
E26.1 Secondary hyperaldosteronism	0.013	0.987	0.000
N95.8 Other specified menopausal and perimenopausal disorders	0.000	0.987	0.013
K86.1 Other chronic pancreatitis	0.012	0.988	0.000
E22.0 Acromegaly and pituitary gigantism	0.012	0.988	0.000
E26.0 Primary hyperaldosteronism	0.012	0.988	0.000
E21 Hyperparathyroidism and other disorders of parathyroid gland	0.012	0.988	0.000
E22.1 Hyperprolactinaemia	0.012	0.988	0.000
E22.9 Hyperfunction of pituitary gland, unspecified	0.012	0.988	0.000
E22.8 Other hyperfunction of pituitary gland	0.012	0.988	0.000
E27.1 Primary adrenocortical insufficiency	0.011	0.989	0.000
C62.9 Testis, unspecified	0.011	0.989	0.000
Z90.3 Acquired absence of part of stomach	0.011	0.989	0.000
E21.5 Disorder of parathyroid gland, unspecified	0.010	0.990	0.000
N13.5 Kinking and stricture of ureter without hydronephrosis	0.010	0.990	0.000
K86.0 Alcohol-induced chronic pancreatitis	0.010	0.990	0.000
K86 Other diseases of pancreas	0.010	0.990	0.000
E21.4 Other specified disorders of parathyroid gland	0.009	0.991	0.000
E21.2 Other hyperparathyroidism	0.009	0.991	0.000
N95.1 Menopausal and female climacteric states	0.000	0.991	0.009
E21.1 Secondary hyperparathyroidism, not elsewhere classified	0.009	0.991	0.000
C15.5 Lower third of oesophagus	0.009	0.991	0.000
E22.2 Syndrome of inappropriate secretion of antidiuretic hormone	0.008	0.992	0.000
K86.8 Other specified diseases of pancreas	0.008	0.992	0.000
K86.3 Pseudocyst of pancreas	0.008	0.992	0.000
Z90 Acquired absence of organs, not elsewhere classified	0.007	0.993	0.000
C15.9 Oesophagus, unspecified	0.007	0.993	0.000
Z90.0 Acquired absence of part of head and neck	0.007	0.993	0.000
Q61.2 Polycystic kidney, adult type	0.007	0.993	0.000
N50.8 Other specified disorders of male genital organs	0.007	0.993	0.000
K86.9 Disease of pancreas, unspecified	0.006	0.994	0.000
E21.3 Hyperparathyroidism, unspecified	0.006	0.994	0.000
Z90.5 Acquired absence of kidney	0.006	0.994	0.000
C15 Malignant neoplasm of oesophagus	0.006	0.994	0.000
C62 Malignant neoplasm of testis	0.006	0.994	0.000
K82.4 Cholesterolosis of gallbladder	0.006	0.994	0.000
Y44.2 Anticoagulants	0.000	0.995	0.005
K13.0 Diseases of lips	0.000	0.995	0.005
E21.0 Primary hyperparathyroidism	0.005	0.995	0.000
C62.1 Descended testis	0.005	0.995	0.000
K70.3 Alcoholic cirrhosis of liver	0.005	0.995	0.000
C15.8 Overlapping lesion of oesophagus	0.004	0.995	0.000
C15.2 Abdominal part of oesophagus	0.004	0.995	0.000
C15.1 Thoracic part of oesophagus	0.004	0.995	0.000
C15.0 Cervical part of oesophagus	0.004	0.995	0.000
C62.0 Undescended testis	0.004	0.995	0.000
K86.2 Cyst of pancreas	0.004	0.995	0.000
K82 Other diseases of gallbladder	0.005	0.995	0.000
R63 Symptoms and signs concerning food and fluid intake	0.000	0.996	0.004
K82.2 Perforation of gallbladder	0.004	0.996	0.000
Z90.8 Acquired absence of other organs	0.004	0.996	0.000
Q61 Cystic kidney disease	0.004	0.996	0.000
K82.3 Fistula of gallbladder	0.004	0.996	0.000
Q89.2 Congenital malformations of other endocrine glands	0.004	0.996	0.000
C15.4 Middle third of oesophagus	0.004	0.996	0.000
R63.8 Other symptoms and signs concerning food and fluid intake	0.000	0.996	0.004
H74.9 Disorder of middle ear and mastoid, unspecified	0.004	0.996	0.000
K70 Alcoholic liver disease	0.004	0.996	0.000
Q76.0 Spina bifida occulta	0.004	0.996	0.000
R63.3 Feeding difficulties and mismanagement	0.000	0.996	0.004
N86 Erosion and ectropion of cervix uteri	0.004	0.996	0.000
R63.1 Polydipsia	0.000	0.996	0.004
C15.3 Upper third of oesophagus	0.003	0.996	0.000
K70.4 Alcoholic hepatic failure	0.003	0.996	0.000
Q61.4 Renal dysplasia	0.003	0.997	0.000
R63.6 Insufficient intake of food and water due to self neglect	0.000	0.997	0.003
R63.2 Polyphagia	0.000	0.997	0.003
H74.0 Tympanosclerosis	0.003	0.997	0.000
H74.2 Discontinuity and dislocation of ear ossicles	0.003	0.997	0.000
K82.9 Disease of gallbladder, unspecified	0.003	0.997	0.000
K70.9 Alcoholic liver disease, unspecified	0.003	0.997	0.000
K82.1 Hydrops of gallbladder	0.003	0.997	0.000
K82.0 Obstruction of gallbladder	0.003	0.997	0.000
H74 Other disorders of middle ear and mastoid	0.003	0.997	0.000
Z90.6 Acquired absence of other parts of urinary tract	0.003	0.997	0.000
K80-K87 Disorders of gallbladder, biliary tract and pancreas	0.003	0.997	0.000
R73.9 Hyperglycaemia, unspecified	0.000	0.997	0.003
Q76 Congenital malformations of spine and bony thorax	0.003	0.997	0.000
Q89 Other congenital malformations, not elsewhere classified	0.003	0.997	0.000
Q61.8 Other cystic kidney diseases	0.003	0.997	0.000
Q61.1 Polycystic kidney, infantile type	0.003	0.997	0.000
K85 Acute pancreatitis	0.003	0.997	0.000
Q60-Q64 Congenital malformations of the urinary system	0.003	0.997	0.000
K70.2 Alcoholic fibrosis and sclerosis of liver	0.003	0.997	0.000
Q61.3 Polycystic kidney, unspecified	0.003	0.997	0.000
M41.99 Scoliosis, unspecified (Site unspecified)	0.000	0.997	0.003
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.003	0.997	0.000
Q61.9 Cystic kidney disease, unspecified	0.003	0.997	0.000
Z83.3 Family history of diabetes mellitus	0.000	0.997	0.003
K85.2 Alcohol-induced acute pancreatitis	0.003	0.997	0.000
Q61.5 Medullary cystic kidney	0.003	0.997	0.000
R63.5 Abnormal weight gain	0.000	0.997	0.003
K70.1 Alcoholic hepatitis	0.003	0.997	0.000
Q89.3 Situs inversus	0.003	0.997	0.000
K85.9 Acute pancreatitis, unspecified	0.003	0.997	0.000
H74.4 Polyp of middle ear	0.003	0.997	0.000
H91.9 Hearing loss, unspecified	0.000	0.997	0.003
K70.0 Alcoholic fatty liver	0.003	0.997	0.000
H74.1 Adhesive middle ear disease	0.003	0.997	0.000
K85.0 Idiopathic acute pancreatitis	0.003	0.997	0.000
B15.9 Hepatitis A without hepatic coma	0.003	0.997	0.000
K87 Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere	0.003	0.997	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.003	0.997	0.000
L57.0 Actinic keratosis	0.003	0.997	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.002	0.997	0.000
Q76.8 Other congenital malformations of bony thorax	0.002	0.997	0.000
Q76.7 Congenital malformation of sternum	0.002	0.997	0.000
Q76.6 Other congenital malformations of ribs	0.002	0.997	0.000
Q76.5 Cervical rib	0.002	0.997	0.000
Q76.3 Congenital scoliosis due to congenital bony malformation	0.002	0.997	0.000
Q76.2 Congenital spondylolisthesis	0.002	0.997	0.000
Q76.1 Klippel-Feil syndrome	0.002	0.997	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.003	0.997	0.000
M35.0 Sicca syndrome [Sjogren]	0.000	0.997	0.003
Q89.9 Congenital malformation, unspecified	0.002	0.997	0.000
Q89.8 Other specified congenital malformations	0.002	0.997	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.002	0.997	0.000
Q89.4 Conjoined twins	0.002	0.997	0.000
Q89.1 Congenital malformations of adrenal gland	0.002	0.997	0.000
Q89.0 Congenital malformations of spleen	0.002	0.997	0.000
Q74.1 Congenital malformation of knee	0.002	0.997	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.997	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.997	0.000
K85.3 Drug-induced acute pancreatitis	0.002	0.997	0.000
Q64 Other congenital malformations of urinary system	0.002	0.997	0.000
D68.3 Haemorrhagic disorder due to circulating anticoagulants	0.000	0.997	0.002
N21.0 Calculus in bladder	0.003	0.997	0.000
N50 Other disorders of male genital organs	0.003	0.997	0.000
Q80-Q89 Other congenital malformations	0.002	0.997	0.000
H74.8 Other specified disorders of middle ear and mastoid	0.002	0.998	0.000
K85.1 Biliary acute pancreatitis	0.002	0.998	0.000
N48.0 Leukoplakia of penis	0.002	0.998	0.000
L40.0 Psoriasis vulgaris	0.000	0.998	0.002
Z39.1 Care and examination of lactating mother	0.000	0.998	0.002
Q62.3 Other obstructive defects of renal pelvis and ureter	0.002	0.998	0.000
Z93.1 Gastrostomy status	0.000	0.998	0.002
B18.1 Chronic viral hepatitis B without delta-agent	0.002	0.998	0.000
H74.3 Other acquired abnormalities of ear ossicles	0.002	0.998	0.000
Q61.0 Congenital single renal cyst	0.002	0.998	0.000
M90.75 Fracture of bone in neoplastic disease (Pelvic region and thigh)	0.002	0.998	0.000
K13.4 Granuloma and granuloma-like lesions of oral mucosa	0.000	0.998	0.002
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
K82.8 Other specified diseases of gallbladder	0.002	0.998	0.000
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
K85.8 Other acute pancreatitis	0.002	0.998	0.000
H90.1 Conductive hearing loss, unilateral with unrestricted hearing on the contralateral side	0.002	0.998	0.000
N50.9 Disorder of male genital organs, unspecified	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
Q60.2 Renal agenesis, unspecified	0.002	0.998	0.000
Q18.0 Sinus, fistula and cyst of branchial cleft	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.002	0.998	0.000
R93.5 Abnormal findings on diagnostic imaging of other abdominal regions, including retroperitoneum	0.002	0.998	0.000
K87.1 Disorders of pancreas in diseases classified elsewhere	0.002	0.998	0.000
K87.0 Disorders of gallbladder and biliary tract in diseases classified elsewhere	0.002	0.998	0.000
Q62.8 Other congenital malformations of ureter	0.002	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.002	0.998	0.000
Q62.6 Malposition of ureter	0.002	0.998	0.000
Q62.4 Agenesis of ureter	0.002	0.998	0.000
Q62.2 Congenital megaloureter	0.002	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.002	0.998	0.000
Q62.0 Congenital hydronephrosis	0.002	0.998	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.002	0.998	0.000
Q73 Reduction defects of unspecified limb	0.002	0.998	0.000
Q72 Reduction defects of lower limb	0.002	0.998	0.000
Q71 Reduction defects of upper limb	0.002	0.998	0.000
Q70 Syndactyly	0.002	0.998	0.000
Q69 Polydactyly	0.002	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
M06.00 Seronegative rheumatoid arthritis (Multiple sites)	0.002	0.998	0.000
Y88.3 Sequelae of surgical and medical procedures as the cause of abnormal reaction of the patient or of later complication, without mention of misadventure at the time of the procedure	0.000	0.998	0.002
Z86.5 Personal history of other mental and behavioural disorders	0.000	0.998	0.002
M48.09 Spinal stenosis (Site unspecified)	0.000	0.998	0.002
Q74.9 Unspecified congenital malformation of limb(s)	0.002	0.998	0.000
Q74.8 Other specified congenital malformations of limb(s)	0.002	0.998	0.000
Q74.3 Arthrogryposis multiplex congenita	0.002	0.998	0.000
Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle	0.002	0.998	0.000
Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle	0.002	0.998	0.000
Q60.6 Potter's syndrome	0.002	0.998	0.000
Q60.5 Renal hypoplasia, unspecified	0.002	0.998	0.000
Q60.4 Renal hypoplasia, bilateral	0.002	0.998	0.000
Q60.3 Renal hypoplasia, unilateral	0.002	0.998	0.000
Q60.1 Renal agenesis, bilateral	0.002	0.998	0.000
M25.61 Stiffness of joint, not elsewhere classified (Shoulder region)	0.002	0.998	0.000
D68.8 Other specified coagulation defects	0.000	0.998	0.002
E16.2 Hypoglycaemia, unspecified	0.000	0.998	0.002
Q18.1 Preauricular sinus and cyst	0.002	0.998	0.000
Q62.5 Duplication of ureter	0.002	0.998	0.000
R25.2 Cramp and spasm	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
L27.1 Localised skin eruption due to drugs and medicaments	0.002	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.002	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.002	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.002	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.002	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.002	0.998	0.000
Q64.4 Malformation of urachus	0.002	0.998	0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.002	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.002	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.002	0.998	0.000
Q64.0 Epispadias	0.002	0.998	0.000
Q66 Congenital deformities of feet	0.002	0.998	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.002	0.998	0.000
Q84 Other congenital malformations of integument	0.002	0.998	0.000
Q81 Epidermolysis bullosa	0.002	0.998	0.000
Q80 Congenital ichthyosis	0.002	0.998	0.000
E53.8 Deficiency of other specified B group vitamins	0.002	0.998	0.000
T82.7 Infection and inflammatory reaction due to other cardiac and vascular devices, implants and grafts	0.000	0.998	0.002
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
I84.7 Unspecified thrombosed haemorrhoids	0.000	0.998	0.002
Q60.0 Renal agenesis, unilateral	0.002	0.998	0.000
C49.2 Connective and soft tissue of lower limb, including hip	0.000	0.998	0.002
Y44 Agents primarily affecting blood constituents	0.000	0.998	0.002
M54.59 Low back pain (Site unspecified)	0.002	0.998	0.000
Q83 Congenital malformations of breast	0.002	0.998	0.000
N50.0 Atrophy of testis	0.002	0.998	0.000
Q63.0 Accessory kidney	0.002	0.998	0.000
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
Q65 Congenital deformities of hip	0.002	0.998	0.000
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
G58.9 Mononeuropathy, unspecified	0.002	0.998	0.000
Q18.9 Congenital malformation of face and neck, unspecified	0.002	0.998	0.000
Q18.8 Other specified congenital malformations of face and neck	0.002	0.998	0.000
Q18.7 Microcheilia	0.002	0.998	0.000
Q18.6 Macrocheilia	0.002	0.998	0.000
Q18.5 Microstomia	0.002	0.998	0.000
Q18.4 Macrostomia	0.002	0.998	0.000
Q18.3 Webbing of neck	0.002	0.998	0.000
Q18.2 Other branchial cleft malformations	0.002	0.998	0.000
Z39.0 Care and examination immediately after delivery	0.000	0.998	0.002
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
F41.0 Panic disorder [episodic paroxysmal anxiety]	0.000	0.998	0.002
R01.1 Cardiac murmur, unspecified	0.000	0.998	0.002
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.002	0.998	0.000
Q15 Other congenital malformations of eye	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
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
K81.0 Acute cholecystitis	0.002	0.998	0.000
Q63.9 Congenital malformation of kidney, unspecified	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.002	0.998	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.002	0.998	0.000
Q82 Other congenital malformations of skin	0.002	0.998	0.000
M43.02 Spondylolysis (Cervical region)	0.002	0.998	0.000
D68.5 Primary Thrombophilia	0.000	0.998	0.002
Q66.3 Other congenital varus deformities of feet	0.002	0.998	0.000
O04.9 Complete or unspecified, without complication	0.000	0.998	0.002
Q68.8 Other specified congenital musculoskeletal deformities	0.002	0.998	0.000
Q68.5 Congenital bowing of long bones of leg, unspecified	0.002	0.998	0.000
Q68.4 Congenital bowing of tibia and fibula	0.002	0.998	0.000
Q68.3 Congenital bowing of femur	0.002	0.998	0.000
Q68.2 Congenital deformity of knee	0.002	0.998	0.000
Q68.1 Congenital deformity of hand	0.002	0.998	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.002	0.998	0.000
Q69.9 Polydactyly, unspecified	0.002	0.998	0.000
Q69.2 Accessory toe(s)	0.002	0.998	0.000
Q69.1 Accessory thumb(s)	0.002	0.998	0.000
Q69.0 Accessory finger(s)	0.002	0.998	0.000
Q70.9 Syndactyly, unspecified	0.002	0.998	0.000
Q70.4 Polysyndactyly	0.002	0.998	0.000
Q70.3 Webbed toes	0.002	0.998	0.000
Q70.2 Fused toes	0.002	0.998	0.000
Q70.1 Webbed fingers	0.002	0.998	0.000
Q70.0 Fused fingers	0.002	0.998	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.002	0.998	0.000
Q71.8 Other reduction defects of upper limb(s)	0.002	0.998	0.000
Q71.6 Lobster-claw hand	0.002	0.998	0.000
Q71.5 Longitudinal reduction defect of ulna	0.002	0.998	0.000
Q71.4 Longitudinal reduction defect of radius	0.002	0.998	0.000
Q71.3 Congenital absence of hand and finger(s)	0.002	0.998	0.000
Q71.2 Congenital absence of both forearm and hand	0.002	0.998	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.002	0.998	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.002	0.998	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.002	0.998	0.000
Q72.8 Other reduction defects of lower limb(s)	0.002	0.998	0.000
Q72.7 Split foot	0.002	0.998	0.000
Q72.6 Longitudinal reduction defect of fibula	0.002	0.998	0.000
Q72.5 Longitudinal reduction defect of tibia	0.002	0.998	0.000
Q72.4 Longitudinal reduction defect of femur	0.002	0.998	0.000
Q72.3 Congenital absence of foot and toe(s)	0.002	0.998	0.000
Q72.2 Congenital absence of both lower leg and foot	0.002	0.998	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.002	0.998	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.002	0.998	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.002	0.998	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.002	0.998	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.002	0.998	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.002	0.998	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.002	0.998	0.000
Q75.5 Oculomandibular dysostosis	0.002	0.998	0.000
Q75.4 Mandibulofacial dysostosis	0.002	0.998	0.000
Q75.3 Macrocephaly	0.002	0.998	0.000
Q75.2 Hypertelorism	0.002	0.998	0.000
Q75.1 Craniofacial dysostosis	0.002	0.998	0.000
Q75.0 Craniosynostosis	0.002	0.998	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.002	0.998	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.002	0.998	0.000
Q77.6 Chondroectodermal dysplasia	0.002	0.998	0.000
Q77.5 Diastrophic dysplasia	0.002	0.998	0.000
Q77.4 Achondroplasia	0.002	0.998	0.000
Q77.3 Chondrodysplasia punctata	0.002	0.998	0.000
Q77.2 Short rib syndrome	0.002	0.998	0.000
Q77.1 Thanatophoric short stature	0.002	0.998	0.000
Q77.0 Achondrogenesis	0.002	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.002	0.998	0.000
M06.01 Seronegative rheumatoid arthritis (Shoulder region)	0.002	0.998	0.000
H53.2 Diplopia	0.000	0.998	0.002
Q66.0 Talipes equinovarus	0.002	0.998	0.000
Z90.2 Acquired absence of lung [part of]	0.002	0.998	0.000
Q12 Congenital lens malformations	0.002	0.998	0.000
Q37 Cleft palate with cleft lip	0.002	0.998	0.000
B15 Acute hepatitis A	0.002	0.998	0.000
U88 Agent resistant to multiple antibiotics	0.000	0.998	0.002
Q67.8 Other congenital deformities of chest	0.002	0.998	0.000
Q67.7 Pectus carinatum	0.002	0.998	0.000
Q67.6 Pectus excavatum	0.002	0.998	0.000
Q67.3 Plagiocephaly	0.002	0.998	0.000
Q67.2 Dolichocephaly	0.002	0.998	0.000
Q67.1 Compression facies	0.002	0.998	0.000
Q67.0 Facial asymmetry	0.002	0.998	0.000
T98.3 Sequelae of complications of surgical and medical care, not elsewhere classified	0.000	0.998	0.002
Q63.2 Ectopic kidney	0.002	0.998	0.000
Q66.9 Congenital deformity of feet, unspecified	0.002	0.998	0.000
Q66.7 Pes cavus	0.002	0.998	0.000
Q66.6 Other congenital valgus deformities of feet	0.002	0.998	0.000
Q66.5 Congenital pes planus	0.002	0.998	0.000
Q66.4 Talipes calcaneovalgus	0.002	0.998	0.000
Q66.2 Metatarsus varus	0.002	0.998	0.000
Q66.1 Talipes calcaneovarus	0.002	0.998	0.000
Q80.9 Congenital ichthyosis, unspecified	0.002	0.998	0.000
Q80.8 Other congenital ichthyosis	0.002	0.998	0.000
Q80.4 Harlequin foetus	0.002	0.998	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.002	0.998	0.000
Q80.2 Lamellar ichthyosis	0.002	0.998	0.000
Q80.1 X-linked ichthyosis	0.002	0.998	0.000
Q80.0 Ichthyosis vulgaris	0.002	0.998	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.002	0.998	0.000
Q81.8 Other epidermolysis bullosa	0.002	0.998	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.002	0.998	0.000
Q81.1 Epidermolysis bullosa letalis	0.002	0.998	0.000
Q81.0 Epidermolysis bullosa simplex	0.002	0.998	0.000
Q84.9 Congenital malformation of integument, unspecified	0.002	0.998	0.000
Q84.8 Other specified congenital malformations of integument	0.002	0.998	0.000
Q84.6 Other congenital malformations of nails	0.002	0.998	0.000
Q84.5 Enlarged and hypertrophic nails	0.002	0.998	0.000
Q84.4 Congenital leukonychia	0.002	0.998	0.000
Q84.3 Anonychia	0.002	0.998	0.000
Q84.2 Other congenital malformations of hair	0.002	0.998	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.002	0.998	0.000
Q84.0 Congenital alopecia	0.002	0.998	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.002	0.998	0.000
Q86.2 Dysmorphism due to warfarin	0.002	0.998	0.000
Q86.1 Foetal hydantoin syndrome	0.002	0.998	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.002	0.998	0.000
R27.0 Ataxia, unspecified	0.000	0.998	0.002
R47.8 Other and unspecified speech disturbances	0.000	0.998	0.002
Q85.8 Other phakomatoses, not elsewhere classified	0.002	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.002	0.998	0.000
R25.8 Other and unspecified abnormal involuntary movements	0.000	0.998	0.002
M79.54 Residual foreign body in soft tissue (Hand)	0.002	0.998	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.002	0.998	0.000
Q79.5 Other congenital malformations of abdominal wall	0.002	0.998	0.000
Q79.4 Prune belly syndrome	0.002	0.998	0.000
Q79.3 Gastroschisis	0.002	0.998	0.000
Q79.2 Exomphalos	0.002	0.998	0.000
Q79.1 Other congenital malformations of diaphragm	0.002	0.998	0.000
Q79.0 Congenital diaphragmatic hernia	0.002	0.998	0.000
I08.3 Combined disorders of mitral, aortic and tricuspid valves	0.000	0.998	0.002
D68 Other coagulation defects	0.000	0.998	0.002
K13 Other diseases of lip and oral mucosa	0.000	0.998	0.002
Q36 Cleft lip	0.002	0.998	0.000
Q35 Cleft palate	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
I79.2 Peripheral angiopathy in diseases classified elsewhere	0.000	0.998	0.002
M06.0 Seronegative rheumatoid arthritis	0.002	0.998	0.000
Q79.8 Other congenital malformations of musculoskeletal system	0.002	0.998	0.000
K81 Cholecystitis	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
M13.94 Arthritis, unspecified (Hand)	0.000	0.998	0.002
Q83.9 Congenital malformation of breast, unspecified	0.001	0.998	0.000
Q83.8 Other congenital malformations of breast	0.001	0.998	0.000
Q83.3 Accessory nipple	0.001	0.998	0.000
Q83.2 Absent nipple	0.001	0.998	0.000
Q83.0 Congenital absence of breast with absent nipple	0.001	0.998	0.000
Y44.9 Other and unspecified agents affecting blood constituents	0.000	0.998	0.002
Y44.7 Plasma substitutes	0.000	0.998	0.002
Y44.6 Natural blood and blood products	0.000	0.998	0.002
Y44.4 Antithrombotic drugs [platelet-aggregation inhibitors]	0.000	0.998	0.002
Y44.3 Anticoagulant antagonists, vitamin K and other coagulants	0.000	0.998	0.002
Y44.1 Vitamin B12, folic acid and other anti-megaloblastic-anaemia preparations	0.000	0.998	0.002
Y44.0 Iron preparations and other anti-hypochromic-anaemia preparations	0.000	0.998	0.002
L27 Dermatitis due to substances taken internally	0.002	0.998	0.000
Q90 Down's syndrome	0.001	0.998	0.000
C49.3 Connective and soft tissue of thorax	0.000	0.998	0.002
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
Q78.2 Osteopetrosis	0.001	0.998	0.000
Q78.1 Polyostotic fibrous dysplasia	0.001	0.998	0.000
Q82.2 Mastocytosis	0.002	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.001	0.998	0.000
Q33 Congenital malformations of lung	0.001	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.001	0.998	0.000
Q31 Congenital malformations of larynx	0.001	0.998	0.000
Q30 Congenital malformations of nose	0.001	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.001	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.001	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.001	0.998	0.000

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