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Variant clusters
Hospitalization Episode Statistics (HES)
Genetic variants: 36,212
Diagnostic terms: × 19,155
Association results: = 693,640,860
Self-Reported Statistics (SRS)
Genetic variants: 28,458
Diagnostic terms: × 474
Association results: = 13,489,092
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Variant-specific associations

rs929641
log Bayes Factor = 0.615574
Chromosome 2   position 58,792,377  (GRCh37) Explore rs929641 on Ensembl!
Variant rs929641 is listed in the   GWAS Catalog   ⇪

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
  
E66.9 Obesity, unspecified
0.000 0.208 0.792
E66 Obesity
0.000 0.261 0.739
E66.8 Other obesity
0.000 0.282 0.718
E66.0 Obesity due to excess calories
0.000 0.407 0.593
E66.1 Drug-induced obesity
0.000 0.470 0.530
E65-E68 Obesity and other hyperalimentation
0.000 0.580 0.420
E66.2 Extreme obesity with alveolar hypoventilation
0.000 0.606 0.394
E65 Localised adiposity
0.000 0.647 0.353
E67 Other hyperalimentation
0.000 0.698 0.301
E68 Sequelae of hyperalimentation
0.000 0.698 0.301
E67.8 Other specified hyperalimentation
0.000 0.784 0.216
E67.3 Hypervitaminosis D
0.000 0.784 0.216
E67.2 Megavitamin-B6 syndrome
0.000 0.784 0.216
E67.1 Hypercarotenaemia
0.000 0.784 0.216
E67.0 Hypervitaminosis A
0.000 0.784 0.216
D21.2 Connective and other soft tissue of lower limb, including hip
0.044 0.956 0.000
E53.8 Deficiency of other specified B group vitamins
0.000 0.957 0.043
E53 Deficiency of other B group vitamins
0.000 0.969 0.031
D21 Other benign neoplasms of connective and other soft tissue
0.029 0.971 0.000
D21.0 Connective and other soft tissue of head, face and neck
0.029 0.971 0.000
E53.9 Vitamin B deficiency, unspecified
0.000 0.977 0.023
D21.3 Connective and other soft tissue of thorax
0.023 0.977 0.000
E53.1 Pyridoxine deficiency
0.000 0.978 0.022
E53.0 Riboflavin deficiency
0.000 0.978 0.022
D21.5 Connective and other soft tissue of pelvis
0.022 0.978 0.000
D21.6 Connective and other soft tissue of trunk, unspecified
0.021 0.979 0.000
D21.4 Connective and other soft tissue of abdomen
0.021 0.979 0.000
E50-E64 Other nutritional deficiencies
0.000 0.979 0.021
Chapter IV Endocrine, nutritional and metabolic diseases
0.000 0.981 0.019
C49 Malignant neoplasm of other connective and soft tissue
0.019 0.981 0.000
C49.2 Connective and soft tissue of lower limb, including hip
0.017 0.982 0.000
C49.9 Connective and soft tissue, unspecified
0.017 0.983 0.000
D21.1 Connective and other soft tissue of upper limb, including shoulder
0.017 0.983 0.000
C49.0 Connective and soft tissue of head, face and neck
0.017 0.983 0.000
D21.9 Connective and other soft tissue, unspecified
0.017 0.983 0.000
C45.0 Mesothelioma of pleura
0.017 0.983 0.000
C45 Mesothelioma
0.016 0.984 0.000
E64 Sequelae of malnutrition and other nutritional deficiencies
0.000 0.984 0.015
E63 Other nutritional deficiencies
0.000 0.984 0.015
E50 Vitamin A deficiency
0.000 0.984 0.015
E60 Dietary zinc deficiency
0.000 0.984 0.015
E59 Dietary selenium deficiency
0.000 0.984 0.015
E54 Ascorbic acid deficiency
0.000 0.984 0.015
E52 Niacin deficiency [pellagra]
0.000 0.984 0.015
E58 Dietary calcium deficiency
0.000 0.985 0.015
E51 Thiamine deficiency
0.000 0.985 0.015
C45-C49 Malignant neoplasms of mesothelial and soft tissue
0.015 0.985 0.000
C45.9 Mesothelioma, unspecified
0.015 0.985 0.000
E56 Other vitamin deficiencies
0.000 0.985 0.015
C49.6 Connective and soft tissue of trunk, unspecified
0.014 0.986 0.000
C49.5 Connective and soft tissue of pelvis
0.014 0.986 0.000
E61 Deficiency of other nutrient elements
0.000 0.986 0.014
C49.3 Connective and soft tissue of thorax
0.014 0.986 0.000
C49.4 Connective and soft tissue of abdomen
0.014 0.986 0.000
C49.8 Overlapping lesion of connective and soft tissue
0.013 0.986 0.000
K76.0 Fatty (change of) liver, not elsewhere classified
0.000 0.987 0.013
E40-E46 Malnutrition
0.000 0.988 0.012
C45.2 Mesothelioma of pericardium
0.012 0.988 0.000
C45.1 Mesothelioma of peritoneum
0.012 0.988 0.000
C49.1 Connective and soft tissue of upper limb, including shoulder
0.011 0.988 0.000
E15-E16 Other disorders of glucose regulation and pancreatic internal secretion
0.000 0.989 0.011
E50.9 Vitamin A deficiency, unspecified
0.000 0.989 0.011
E50.8 Other manifestations of vitamin A deficiency
0.000 0.989 0.011
E50.7 Other ocular manifestations of vitamin A deficiency
0.000 0.989 0.011
E50.6 Vitamin A deficiency with xerophthalmic scars of cornea
0.000 0.989 0.011
E50.5 Vitamin A deficiency with night blindness
0.000 0.989 0.011
E50.4 Vitamin A deficiency with keratomalacia
0.000 0.989 0.011
E50.3 Vitamin A deficiency with corneal ulceration and xerosis
0.000 0.989 0.011
E50.2 Vitamin A deficiency with corneal xerosis
0.000 0.989 0.011
E50.1 Vitamin A deficiency with Bitot's spot and conjunctival xerosis
0.000 0.989 0.011
E50.0 Vitamin A deficiency with conjunctival xerosis
0.000 0.989 0.011
E63.9 Nutritional deficiency, unspecified
0.000 0.989 0.011
E63.8 Other specified nutritional deficiencies
0.000 0.989 0.011
E63.1 Imbalance of constituents of food intake
0.000 0.989 0.011
E63.0 Essential fatty acid [EFA] deficiency
0.000 0.989 0.011
E64.9 Sequelae of unspecified nutritional deficiency
0.000 0.989 0.011
E64.8 Sequelae of other nutritional deficiencies
0.000 0.989 0.011
E64.3 Sequelae of rickets
0.000 0.989 0.011
E64.2 Sequelae of vitamin C deficiency
0.000 0.989 0.011
E64.1 Sequelae of vitamin A deficiency
0.000 0.989 0.011
E64.0 Sequelae of protein-energy malnutrition
0.000 0.989 0.011
E55 Vitamin D deficiency
0.000 0.989 0.011
E51.9 Thiamine deficiency, unspecified
0.000 0.989 0.011
E51.8 Other manifestations of thiamine deficiency
0.000 0.989 0.011
E51.1 Beriberi
0.000 0.989 0.011
C47 Malignant neoplasm of peripheral nerves and autonomic nervous system
0.011 0.989 0.000
C46 Kaposi's sarcoma
0.011 0.989 0.000
E51.2 Wernicke's encephalopathy
0.000 0.989 0.011
E61.2 Magnesium deficiency
0.000 0.989 0.011
E56.9 Vitamin deficiency, unspecified
0.000 0.989 0.011
E56.8 Deficiency of other vitamins
0.000 0.989 0.011
E56.0 Deficiency of vitamin E
0.000 0.989 0.011
E56.1 Deficiency of vitamin K
0.000 0.990 0.010
E61.9 Deficiency of nutrient element, unspecified
0.000 0.990 0.010
E61.8 Deficiency of other specified nutrient elements
0.000 0.990 0.010
E61.7 Deficiency of multiple nutrient elements
0.000 0.990 0.010
E61.6 Vanadium deficiency
0.000 0.990 0.010
E61.5 Molybdenum deficiency
0.000 0.990 0.010
E61.4 Chromium deficiency
0.000 0.990 0.010
E61.3 Manganese deficiency
0.000 0.990 0.010
E61.0 Copper deficiency
0.000 0.990 0.010
C48 Malignant neoplasm of retroperitoneum and peritoneum
0.010 0.990 0.000
C45.7 Mesothelioma of other sites
0.009 0.991 0.000
Q21.1 Atrial septal defect
0.009 0.991 0.000
I67.8 Other specified cerebrovascular diseases
0.009 0.991 0.000
M88.99 Paget's disease of bone, unspecified (Site unspecified)
0.009 0.991 0.000
E44 Protein-energy malnutrition of moderate and mild degree
0.000 0.991 0.009
E45 Retarded development following protein-energy malnutrition
0.000 0.991 0.009
E43 Unspecified severe protein-energy malnutrition
0.000 0.991 0.009
E42 Marasmic kwashiorkor
0.000 0.991 0.009
E41 Nutritional marasmus
0.000 0.991 0.009
E40 Kwashiorkor
0.000 0.991 0.009
M88.9 Paget's disease of bone, unspecified
0.009 0.991 0.000
O34.2 Maternal care due to uterine scar from previous surgery
0.009 0.991 0.000
E15 Nondiabetic hypoglycaemic coma
0.000 0.992 0.008
E55.0 Rickets, active
0.000 0.992 0.008
Q21 Congenital malformations of cardiac septa
0.008 0.992 0.000
C46.9 Kaposi's sarcoma, unspecified
0.008 0.992 0.000
C46.8 Kaposi's sarcoma of multiple organs
0.008 0.992 0.000
C46.7 Kaposi's sarcoma of other sites
0.008 0.992 0.000
C46.3 Kaposi's sarcoma of lymph nodes
0.008 0.992 0.000
C46.2 Kaposi's sarcoma of palate
0.008 0.992 0.000
C46.1 Kaposi's sarcoma of soft tissue
0.008 0.992 0.000
C46.0 Kaposi's sarcoma of skin
0.008 0.992 0.000
C47.9 Peripheral nerves and autonomic nervous system, unspecified
0.008 0.992 0.000
C47.8 Overlapping lesion of peripheral nerves and autonomic nervous system
0.008 0.992 0.000
C47.6 Peripheral nerves of trunk, unspecified
0.008 0.992 0.000
C47.5 Peripheral nerves of pelvis
0.008 0.992 0.000
C47.4 Peripheral nerves of abdomen
0.008 0.992 0.000
C47.3 Peripheral nerves of thorax
0.008 0.992 0.000
C47.2 Peripheral nerves of lower limb, including hip
0.008 0.992 0.000
C47.1 Peripheral nerves of upper limb, including shoulder
0.008 0.992 0.000
C47.0 Peripheral nerves of head, face and neck
0.008 0.992 0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities
0.008 0.992 0.000
Q20-Q28 Congenital malformations of the circulatory system
0.008 0.992 0.000
Q80-Q89 Other congenital malformations
0.008 0.992 0.000
E28.2 Polycystic ovarian syndrome
0.008 0.992 0.000
M88.90 Paget's disease of bone, unspecified (Multiple sites)
0.008 0.992 0.000
Z34.8 Supervision of other normal pregnancy
0.008 0.992 0.000
C48.2 Peritoneum, unspecified
0.008 0.992 0.000
I71.9 Aortic aneurysm of unspecified site, without mention of rupture
0.008 0.992 0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
0.008 0.992 0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck
0.008 0.992 0.000
Q83 Congenital malformations of breast
0.008 0.992 0.000
M88 Paget's disease of bone [osteitis deformans]
0.008 0.992 0.000
C48.8 Overlapping lesion of retroperitoneum and peritoneum
0.007 0.993 0.000
Q00-Q07 Congenital malformations of the nervous system
0.007 0.993 0.000
Q25 Congenital malformations of great arteries
0.007 0.993 0.000
E46 Unspecified protein-energy malnutrition
0.000 0.993 0.007
Q83.3 Accessory nipple
0.007 0.993 0.000
Q27 Other congenital malformations of peripheral vascular system
0.007 0.993 0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems
0.007 0.993 0.000
E61.1 Iron deficiency
0.000 0.993 0.007
Q96 Turner's syndrome
0.007 0.993 0.000
E27.4 Other and unspecified adrenocortical insufficiency
0.007 0.993 0.000
E27.1 Primary adrenocortical insufficiency
0.007 0.993 0.000
H44.2 Degenerative myopia
0.007 0.993 0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
0.007 0.993 0.000
Q22 Congenital malformations of pulmonary and tricuspid valves
0.007 0.993 0.000
C48.1 Specified parts of peritoneum
0.006 0.993 0.000
E44.1 Mild protein-energy malnutrition
0.000 0.993 0.006
E44.0 Moderate protein-energy malnutrition
0.000 0.993 0.006
Q05 Spina bifida
0.006 0.993 0.000
Q27.3 Peripheral arteriovenous malformation
0.006 0.993 0.000
Q14 Congenital malformations of posterior segment of eye
0.006 0.993 0.000
E27 Other disorders of adrenal gland
0.006 0.993 0.000
M88.98 Paget's disease of bone, unspecified (Other)
0.006 0.994 0.000
M88.97 Paget's disease of bone, unspecified (Ankle and foot)
0.006 0.994 0.000
M88.96 Paget's disease of bone, unspecified (Lower leg)
0.006 0.994 0.000
M88.94 Paget's disease of bone, unspecified (Hand)
0.006 0.994 0.000
M88.93 Paget's disease of bone, unspecified (Forearm)
0.006 0.994 0.000
M88.92 Paget's disease of bone, unspecified (Upper arm)
0.006 0.994 0.000
M88.91 Paget's disease of bone, unspecified (Shoulder region)
0.006 0.994 0.000
Q30-Q34 Congenital malformations of the respiratory system
0.006 0.994 0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
0.006 0.994 0.000
Q12 Congenital lens malformations
0.006 0.994 0.000
Q80 Congenital ichthyosis
0.006 0.994 0.000
M88.95 Paget's disease of bone, unspecified (Pelvic region and thigh)
0.006 0.994 0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit
0.006 0.994 0.000
Q35-Q37 Cleft lip and cleft palate
0.006 0.994 0.000
Q21.9 Congenital malformation of cardiac septum, unspecified
0.006 0.994 0.000
Q82 Other congenital malformations of skin
0.006 0.994 0.000
Q21.8 Other congenital malformations of cardiac septa
0.006 0.994 0.000
Q21.4 Aortopulmonary septal defect
0.006 0.994 0.000
Q21.2 Atrioventricular septal defect
0.006 0.994 0.000
Q90 Down's syndrome
0.006 0.994 0.000
Q96.9 Turner's syndrome, unspecified
0.006 0.994 0.000
Q26 Congenital malformations of great veins
0.006 0.994 0.000
Q85 Phakomatoses, not elsewhere classified
0.006 0.994 0.000
Q21.3 Tetralogy of Fallot
0.006 0.994 0.000
M86-M90 Other osteopathies
0.006 0.994 0.000
C48.0 Retroperitoneum
0.006 0.994 0.000
Q05.9 Spina bifida, unspecified
0.006 0.994 0.000
Q25.7 Other congenital malformations of pulmonary artery
0.006 0.994 0.000
M88.0 Paget's disease of skull
0.006 0.994 0.000
M88.8 Paget's disease of other bones
0.006 0.994 0.000
Q20 Congenital malformations of cardiac chambers and connexions
0.006 0.994 0.000
E16 Other disorders of pancreatic internal secretion
0.000 0.994 0.006
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
0.006 0.994 0.000
Q84 Other congenital malformations of integument
0.006 0.994 0.000
Q81 Epidermolysis bullosa
0.006 0.994 0.000
Q83.1 Accessory breast
0.006 0.994 0.000
Q18 Other congenital malformations of face and neck
0.006 0.994 0.000
M89.9 Disorder of bone, unspecified
0.006 0.994 0.000
Q25.1 Coarctation of aorta
0.006 0.994 0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest
0.006 0.994 0.000
Q83.8 Other congenital malformations of breast
0.006 0.994 0.000
Q25.4 Other congenital malformations of aorta
0.006 0.994 0.000
Q07 Other congenital malformations of nervous system
0.006 0.994 0.000
E28 Ovarian dysfunction
0.006 0.994 0.000
Q50-Q56 Congenital malformations of genital organs
0.006 0.994 0.000
E27.2 Addisonian crisis
0.006 0.994 0.000
Q21.0 Ventricular septal defect
0.006 0.994 0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
0.006 0.994 0.000
Q28 Other congenital malformations of circulatory system
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
O99.8 Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
0.006 0.994 0.000
Q14.1 Congenital malformation of retina
0.006 0.994 0.000
Q83.9 Congenital malformation of breast, unspecified
0.006 0.994 0.000
Q83.2 Absent nipple
0.006 0.994 0.000
Q83.0 Congenital absence of breast with absent nipple
0.006 0.994 0.000
C73 Malignant neoplasm of thyroid gland
0.000 0.994 0.006
Q16 Congenital malformations of ear causing impairment of hearing
0.006 0.994 0.000
Q13 Congenital malformations of anterior segment of eye
0.006 0.994 0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos
0.006 0.994 0.000
M90 Osteopathies in diseases classified elsewhere
0.006 0.994 0.000
Q22.5 Ebstein's anomaly
0.006 0.994 0.000
Q99 Other chromosome abnormalities, not elsewhere classified
0.006 0.994 0.000
M86 Osteomyelitis
0.006 0.994 0.000
Q51.3 Bicornate uterus
0.006 0.994 0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified
0.006 0.994 0.000
I71.3 Abdominal aortic aneurysm, ruptured
0.006 0.994 0.000
Q60-Q64 Congenital malformations of the urinary system
0.006 0.994 0.000
Q15 Other congenital malformations of eye
0.005 0.994 0.000
Q12.0 Congenital cataract
0.005 0.994 0.000
Q98.4 Klinefelter's syndrome, unspecified
0.005 0.994 0.000
Q76 Congenital malformations of spine and bony thorax
0.005 0.994 0.000
Q89 Other congenital malformations, not elsewhere classified
0.005 0.994 0.000
Q06 Other congenital malformations of spinal cord
0.005 0.995 0.000
Q04 Other congenital malformations of brain
0.005 0.995 0.000
Q01 Encephalocele
0.005 0.995 0.000
Q00 Anencephaly and similar malformations
0.005 0.995 0.000
Q02 Microcephaly
0.005 0.995 0.000
Q25.3 Stenosis of aorta
0.005 0.995 0.000
Q82.5 Congenital nonneoplastic naevus
0.005 0.995 0.000
M89 Other disorders of bone
0.005 0.995 0.000
M89.95 Disorder of bone, unspecified (Pelvic region and thigh)
0.005 0.995 0.000
Q10.0 Congenital ptosis
0.005 0.995 0.000
Q17 Other congenital malformations of ear
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
M89.90 Disorder of bone, unspecified (Multiple sites)
0.005 0.995 0.000
Q51 Congenital malformations of uterus and cervix
0.005 0.995 0.000
Q60 Renal agenesis and other reduction defects of kidney
0.005 0.995 0.000
S22.40 Multiple fractures of ribs (closed)
0.005 0.995 0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
0.005 0.995 0.000
Q78 Other osteochondrodysplasias
0.005 0.995 0.000
M90.1 Periostitis in other infectious diseases classified elsewhere
0.005 0.995 0.000
Q74 Other congenital malformations of limb(s)
0.005 0.995 0.000
O73.0 Retained placenta, without haemorrhage
0.005 0.995 0.000
Q27.4 Congenital phlebectasia
0.005 0.995 0.000
Q27.2 Other congenital malformations of renal artery
0.005 0.995 0.000
Q27.1 Congenital renal artery stenosis
0.005 0.995 0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery
0.005 0.995 0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature
0.005 0.995 0.000
Q90.9 Down's syndrome, unspecified
0.005 0.995 0.000
M89.98 Disorder of bone, unspecified (Other)
0.005 0.995 0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes
0.005 0.995 0.000
Q87.3 Congenital malformation syndromes involving early overgrowth
0.005 0.995 0.000
M89.92 Disorder of bone, unspecified (Upper arm)
0.005 0.995 0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs
0.005 0.995 0.000
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
Q80.9 Congenital ichthyosis, unspecified
0.005 0.995 0.000
Q35 Cleft palate
0.005 0.995 0.000
E20-E35 Disorders of other endocrine glands
0.005 0.995 0.001
M88.00 Paget's disease of skull-Mult sites
0.005 0.995 0.000
M86.6 Other chronic osteomyelitis
0.005 0.995 0.000
Q23 Congenital malformations of aortic and mitral valves
0.005 0.995 0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
0.005 0.995 0.000
Q75 Other congenital malformations of skull and face bones
0.005 0.995 0.000
Q73 Reduction defects of unspecified limb
0.005 0.995 0.000
Q72 Reduction defects of lower limb
0.005 0.995 0.000
Q71 Reduction defects of upper limb
0.005 0.995 0.000
Q70 Syndactyly
0.005 0.995 0.000
Q69 Polydactyly
0.005 0.995 0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified
0.005 0.995 0.000
Q22.8 Other congenital malformations of tricuspid valve
0.005 0.995 0.000
Q22.6 Hypoplastic right heart syndrome
0.005 0.995 0.000
Q22.4 Congenital tricuspid stenosis
0.005 0.995 0.000
Q22.3 Other congenital malformations of pulmonary valve
0.005 0.995 0.000
Q22.2 Congenital pulmonary valve insufficiency
0.005 0.995 0.000
Q22.1 Congenital pulmonary valve stenosis
0.005 0.995 0.000
Q22.0 Pulmonary valve atresia
0.005 0.995 0.000
Q85.8 Other phakomatoses, not elsewhere classified
0.005 0.995 0.000
M88.85 Paget's disease of other bones (Pelvic region and thigh)
0.005 0.995 0.000
Q87.4 Marfan's syndrome
0.005 0.995 0.000
E27.3 Drug-induced adrenocortical insufficiency
0.005 0.995 0.000
Q05.4 Unspecified spina bifida with hydrocephalus
0.005 0.995 0.000
Q67.6 Pectus excavatum
0.005 0.995 0.000
Q31 Congenital malformations of larynx
0.005 0.995 0.000
Q18.0 Sinus, fistula and cyst of branchial cleft
0.005 0.995 0.000
M90.10 Periostitis in other infectious diseases classified elsewhere (Multiple sites)
0.005 0.995 0.000
Q67.5 Congenital deformity of spine
0.005 0.995 0.000
Q03 Congenital hydrocephalus
0.005 0.995 0.000
Q85.9 Phakomatosis, unspecified
0.005 0.995 0.000
I71 Aortic aneurysm and dissection
0.005 0.995 0.000
Q30 Congenital malformations of nose
0.005 0.995 0.000
Q68 Other congenital musculoskeletal deformities
0.005 0.995 0.000
M89.94 Disorder of bone, unspecified (Hand)
0.005 0.995 0.000
Q05.8 Sacral spina bifida without hydrocephalus
0.005 0.995 0.000
Q05.6 Thoracic spina bifida without hydrocephalus
0.005 0.995 0.000
Q05.5 Cervical spina bifida without hydrocephalus
0.005 0.995 0.000
Q05.3 Sacral spina bifida with hydrocephalus
0.005 0.995 0.000
Q05.2 Lumbar spina bifida with hydrocephalus
0.005 0.995 0.000
Q05.1 Thoracic spina bifida with hydrocephalus
0.005 0.995 0.000
Q05.0 Cervical spina bifida with hydrocephalus
0.005 0.995 0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified
0.005 0.995 0.000
Q14.8 Other congenital malformations of posterior segment of eye
0.005 0.995 0.000
Q14.3 Congenital malformation of choroid
0.005 0.995 0.000
Q14.2 Congenital malformation of optic disk
0.005 0.995 0.000
Q14.0 Congenital malformation of vitreous humour
0.005 0.995 0.000
E27.5 Adrenomedullary hyperfunction
0.005 0.995 0.000
E27.0 Other adrenocortical overactivity
0.005 0.995 0.000
E16.0 Drug-induced hypoglycaemia without coma
0.000 0.995 0.005
Q26.4 Anomalous pulmonary venous connexion, unspecified
0.005 0.995 0.000
E34 Other endocrine disorders
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
Q27.9 Congenital malformation of peripheral vascular system, unspecified
0.005 0.995 0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified
0.005 0.995 0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype
0.005 0.995 0.000
Q98.7 Male with sex chromosome mosaicism
0.005 0.995 0.000
Q98.6 Male with structurally abnormal sex chromosome
0.005 0.995 0.000
Q98.5 Karyotype 47,XYY
0.005 0.995 0.000
Q98.3 Other male with 46,XX karyotype
0.005 0.995 0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype
0.005 0.995 0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes
0.005 0.995 0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY
0.005 0.995 0.000
Q07.0 Arnold-Chiari syndrome
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
Q67.4 Other congenital deformities of skull, face and jaw
0.005 0.995 0.000
Q80.8 Other congenital ichthyosis
0.005 0.995 0.000
Q80.4 Harlequin foetus
0.005 0.995 0.000
Q80.3 Congenital bullous ichthyosiform erythroderma
0.005 0.995 0.000
Q80.2 Lamellar ichthyosis
0.005 0.995 0.000
Q80.1 X-linked ichthyosis
0.005 0.995 0.000
Q80.0 Ichthyosis vulgaris
0.005 0.995 0.000
Q28.3 Other malformations of cerebral vessels
0.005 0.995 0.000
E34.8 Other specified endocrine disorders
0.005 0.995 0.000
Q27.8 Other specified congenital malformations of peripheral vascular system
0.005 0.995 0.000
Q82.2 Mastocytosis
0.005 0.995 0.000
Q10.7 Congenital malformation of orbit
0.005 0.995 0.000
Q10.6 Other congenital malformations of lachrymal apparatus
0.005 0.995 0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct
0.005 0.995 0.000
Q10.4 Absence and agenesis of lachrymal apparatus
0.005 0.995 0.000
Q10.3 Other congenital malformations of eyelid
0.005 0.995 0.000
Q10.2 Congenital entropion
0.005 0.995 0.000
Q10.1 Congenital ectropion
0.005 0.995 0.000
Q36 Cleft lip
0.005 0.995 0.000
Q05.7 Lumbar spina bifida without hydrocephalus
0.005 0.995 0.000
E16.1 Other hypoglycaemia
0.000 0.995 0.005
Q82.9 Congenital malformation of skin, unspecified
0.005 0.995 0.000
Q82.4 Ectodermal dysplasia (anhidrotic)
0.005 0.995 0.000
Q82.3 Incontinentia pigmenti
0.005 0.995 0.000
Q82.1 Xeroderma pigmentosum
0.005 0.995 0.000
M90.6 Osteitis deformans in neoplastic disease
0.005 0.995 0.000
Q26.9 Congenital malformation of great vein, unspecified
0.005 0.995 0.000
Q26.8 Other congenital malformations of great veins
0.005 0.995 0.000
Q26.6 Portal vein-hepatic artery fistula
0.005 0.995 0.000
Q26.5 Anomalous portal venous connexion
0.005 0.995 0.000
Q26.3 Partial anomalous pulmonary venous connexion
0.005 0.995 0.000
Q26.2 Total anomalous pulmonary venous connexion
0.005 0.995 0.000
Q26.1 Persistent left superior vena cava
0.005 0.995 0.000
Q26.0 Congenital stenosis of vena cava
0.005 0.995 0.000
Q85.1 Tuberous sclerosis
0.005 0.995 0.000
Q90.2 Trisomy 21, translocation
0.005 0.995 0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
0.005 0.995 0.000
Q90.0 Trisomy 21, meiotic nondisjunction
0.005 0.995 0.000
Q76.5 Cervical rib
0.005 0.995 0.000
E27.9 Disorder of adrenal gland, unspecified
0.005 0.995 0.000
Q76.4 Other congenital malformations of spine, not associated with scoliosis
0.005 0.995 0.000
Q07.8 Other specified congenital malformations of nervous system
0.005 0.995 0.000
Q25.6 Stenosis of pulmonary artery
0.004 0.995 0.000
Q25.0 Patent ductus arteriosus
0.004 0.995 0.000
Q55 Other congenital malformations of male genital organs
0.005 0.995 0.000
M88.09 Paget's disease of skull-Site unspec
0.004 0.995 0.000
M88.08 Paget's disease of skull-Other
0.004 0.995 0.000
M88.07 Paget's disease of skull-Ankle/Foot
0.004 0.995 0.000
M88.06 Paget's disease of skull-Lower Leg
0.004 0.995 0.000
M88.05 Paget's disease of skull-Pelvic/Thigh
0.004 0.995 0.000
M88.04 Paget's disease of skull-Hand
0.004 0.995 0.000
M88.03 Paget's disease of skull-Forearm
0.004 0.995 0.000
M88.02 Paget's disease of skull-Upper arm
0.004 0.995 0.000
M88.01 Paget's disease of skull-Shldr region
0.004 0.995 0.000
M88.89 Paget's disease of other bones (Site unspecified)
0.004 0.995 0.000
M88.88 Paget's disease of other bones (Other)
0.004 0.995 0.000
M88.87 Paget's disease of other bones (Ankle and foot)
0.004 0.995 0.000
M88.86 Paget's disease of other bones (Lower leg)
0.004 0.995 0.000
M88.84 Paget's disease of other bones (Hand)
0.004 0.995 0.000
M88.83 Paget's disease of other bones (Forearm)
0.004 0.995 0.000
M88.82 Paget's disease of other bones (Upper arm)
0.004 0.995 0.000
M88.81 Paget's disease of other bones (Shoulder region)
0.004 0.995 0.000
M88.80 Paget's disease of other bones (Multiple sites)
0.004 0.995 0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified
0.004 0.995 0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions
0.004 0.995 0.000
Q20.6 Isomerism of atrial appendages
0.004 0.995 0.000
Q20.5 Discordant atrioventricular connexion
0.004 0.995 0.000
Q20.4 Double inlet ventricle
0.004 0.995 0.000
Q20.3 Discordant ventriculoarterial connexion
0.004 0.995 0.000
Q20.2 Double outlet left ventricle
0.004 0.995 0.000
Q20.1 Double outlet right ventricle
0.004 0.995 0.000
Q20.0 Common arterial trunk
0.004 0.995 0.000
S22.4 Multiple fractures of ribs
0.005 0.995 0.000
M86.67 Other chronic osteomyelitis (Ankle and foot)
0.005 0.995 0.000
E16.9 Disorder of pancreatic internal secretion, unspecified
0.000 0.995 0.004
E16.8 Other specified disorders of pancreatic internal secretion
0.000 0.995 0.004
E16.4 Abnormal secretion of gastrin
0.000 0.995 0.004
E16.3 Increased secretion of glucagon
0.000 0.995 0.004
Q23.3 Congenital mitral insufficiency
0.004 0.995 0.000
Q81.9 Epidermolysis bullosa, unspecified
0.004 0.995 0.000
Q81.8 Other epidermolysis bullosa
0.004 0.995 0.000
Q81.2 Epidermolysis bullosa dystrophica
0.004 0.995 0.000
Q81.1 Epidermolysis bullosa letalis
0.004 0.995 0.000
Q81.0 Epidermolysis bullosa simplex
0.004 0.995 0.000
Q84.9 Congenital malformation of integument, unspecified
0.004 0.995 0.000
Q84.8 Other specified congenital malformations of integument
0.004 0.995 0.000
Q84.6 Other congenital malformations of nails
0.004 0.995 0.000
Q84.5 Enlarged and hypertrophic nails
0.004 0.995 0.000
Q84.4 Congenital leukonychia
0.004 0.995 0.000
Q84.3 Anonychia
0.004 0.995 0.000
Q84.2 Other congenital malformations of hair
0.004 0.995 0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified
0.004 0.995 0.000
Q84.0 Congenital alopecia
0.004 0.995 0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes
0.004 0.995 0.000
Q86.2 Dysmorphism due to warfarin
0.004 0.995 0.000
Q86.1 Foetal hydantoin syndrome
0.004 0.995 0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)
0.004 0.995 0.000
M89.99 Disorder of bone, unspecified (Site unspecified)
0.005 0.995 0.000
Q18.9 Congenital malformation of face and neck, unspecified
0.004 0.995 0.000
Q18.8 Other specified congenital malformations of face and neck
0.004 0.995 0.000
Q18.7 Microcheilia
0.004 0.995 0.000
Q18.6 Macrocheilia
0.004 0.995 0.000
Q18.5 Microstomia
0.004 0.995 0.000
Q18.4 Macrostomia
0.004 0.995 0.000
Q18.3 Webbing of neck
0.004 0.995 0.000
Q18.2 Other branchial cleft malformations
0.004 0.995 0.000
Q79.6 Ehlers-Danlos syndrome
0.005 0.995 0.000
Q37 Cleft palate with cleft lip
0.004 0.995 0.000
M89.96 Disorder of bone, unspecified (Lower leg)
0.005 0.995 0.000
M89.93 Disorder of bone, unspecified (Forearm)
0.004 0.995 0.000
M90.8 Osteopathy in other diseases classified elsewhere
0.004 0.995 0.000
Q67.8 Other congenital deformities of chest
0.004 0.995 0.000
Q67.7 Pectus carinatum
0.004 0.995 0.000
Q67.3 Plagiocephaly
0.004 0.995 0.000
Q67.2 Dolichocephaly
0.004 0.995 0.000
Q67.1 Compression facies
0.004 0.995 0.000
Q67.0 Facial asymmetry
0.004 0.995 0.000
Q60.2 Renal agenesis, unspecified
0.005 0.995 0.000
B95.4 Other streptococcus as the cause of diseases classified to other chapters
0.005 0.995 0.000
M89.91 Disorder of bone, unspecified (Shoulder region)
0.004 0.995 0.000
E28.9 Ovarian dysfunction, unspecified
0.004 0.995 0.000
E28.8 Other ovarian dysfunction
0.004 0.995 0.000
E28.1 Androgen excess
0.004 0.995 0.000
E28.0 Oestrogen excess
0.004 0.995 0.000
Q07.9 Congenital malformation of nervous system, unspecified
0.004 0.995 0.000
Q60.0 Renal agenesis, unilateral
0.004 0.995 0.000
Q56 Indeterminate sex and pseudohermaphroditism
0.004 0.995 0.000
Q52 Other congenital malformations of female genitalia
0.004 0.995 0.000
Q18.1 Preauricular sinus and cyst
0.004 0.995 0.000
Q79.8 Other congenital malformations of musculoskeletal system
0.004 0.995 0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
0.004 0.995 0.000
M86.1 Other acute osteomyelitis
0.004 0.995 0.000
M89.3 Hypertrophy of bone
0.004 0.996 0.000
M86.9 Osteomyelitis, unspecified
0.004 0.996 0.000
Q28.9 Congenital malformation of circulatory system, unspecified
0.004 0.996 0.000
Q28.8 Other specified congenital malformations of circulatory system
0.004 0.996 0.000
Q28.1 Other malformations of precerebral vessels
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

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.

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