TreeWAS – Variant ID: rs10036748

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
H60.9 Otitis externa, unspecified	0.000	0.975	0.025
H60 Otitis externa	0.000	0.976	0.024
H61.8 Other specified disorders of external ear	0.000	0.979	0.021
H60.3 Other infective otitis externa	0.000	0.980	0.020
H60.4 Cholesteatoma of external ear	0.000	0.980	0.020
H60-H62 Diseases of external ear	0.000	0.980	0.020
H61 Other disorders of external ear	0.000	0.981	0.019
H60.5 Acute otitis externa, non-infective	0.000	0.981	0.019
H60.8 Other otitis externa	0.000	0.982	0.018
H60.1 Cellulitis of external ear	0.000	0.982	0.017
H60.2 Malignant otitis externa	0.000	0.983	0.017
H60.0 Abscess of external ear	0.000	0.983	0.017
H61.3 Acquired stenosis of external ear canal	0.000	0.984	0.016
S83.6 Sprain and strain of other and unspecified parts of knee	0.016	0.984	0.000
S83 Dislocation, sprain and strain of joints and ligaments of knee	0.015	0.985	0.000
S83.5 Sprain and strain involving (anterior)(posterior) cruciate ligament of knee	0.015	0.985	0.000
S83.2 Tear of meniscus, current	0.014	0.986	0.000
H62 Disorders of external ear in diseases classified elsewhere	0.000	0.986	0.014
H61.1 Non-infective disorders of pinna	0.000	0.986	0.014
S83.4 Sprain and strain involving (fibular)(tibial) collateral ligamnent of knee	0.013	0.987	0.000
H61.9 Disorder of external ear, unspecified	0.000	0.987	0.013
H61.2 Impacted cerumen	0.000	0.987	0.013
S83.0 Dislocation of patella	0.012	0.988	0.000
H61.0 Perichondritis of external ear	0.000	0.988	0.011
S83.3 Tear of articular cartilage of knee, current	0.011	0.989	0.000
S83.1 Dislocation of knee	0.011	0.989	0.000
S83.7 Injury to multiple structures of knee	0.011	0.989	0.000
D52.9 Folate deficiency anaemia, unspecified	0.011	0.989	0.000
H62.8 Other disorders of external ear in diseases classified elsewhere	0.000	0.990	0.010
H62.4 Otitis externa in other diseases classified elsewhere	0.000	0.990	0.010
H62.3 Otitis externa in other infectious and parasitic diseases classified elsewhere	0.000	0.990	0.010
H62.2 Otitis externa in mycoses	0.000	0.990	0.010
H62.1 Otitis externa in viral diseases classified elsewhere	0.000	0.990	0.010
H62.0 Otitis externa in bacterial diseases classified elsewhere	0.000	0.990	0.009
E27.1 Primary adrenocortical insufficiency	0.009	0.991	0.000
E27 Other disorders of adrenal gland	0.008	0.992	0.000
E27.9 Disorder of adrenal gland, unspecified	0.008	0.992	0.000
E27.4 Other and unspecified adrenocortical insufficiency	0.008	0.992	0.000
E27.2 Addisonian crisis	0.007	0.993	0.000
S06.60 Traumatic subarachnoid haemorrhage (without open intracranial wound)	0.000	0.994	0.006
E27.5 Adrenomedullary hyperfunction	0.006	0.994	0.000
E27.0 Other adrenocortical overactivity	0.006	0.994	0.000
J33.9 Nasal polyp, unspecified	0.000	0.994	0.006
E27.3 Drug-induced adrenocortical insufficiency	0.006	0.994	0.000
D04.3 Skin of other and unspecified parts of face	0.006	0.994	0.000
M35.0 Sicca syndrome [Sjogren]	0.005	0.995	0.000
G82.5 Tetraplegia, unspecified	0.005	0.995	0.000
H66.9 Otitis media, unspecified	0.000	0.995	0.005
D52 Folate deficiency anaemia	0.005	0.995	0.000
G82 Paraplegia and tetraplegia	0.005	0.995	0.000
K90.0 Coeliac disease	0.000	0.995	0.005
E27.8 Other specified disorders of adrenal gland	0.004	0.995	0.000
H72.9 Perforation of tympanic membrane, unspecified	0.000	0.995	0.005
G82.1 Spastic paraplegia	0.004	0.996	0.000
E20-E35 Disorders of other endocrine glands	0.004	0.996	0.000
H72 Perforation of tympanic membrane	0.000	0.996	0.004
H66 Suppurative and unspecified otitis media	0.000	0.996	0.004
E24 Cushing's syndrome	0.004	0.996	0.000
H65-H75 Diseases of middle ear and mastoid	0.000	0.996	0.004
E23 Hypofunction and other disorders of pituitary gland	0.004	0.996	0.000
Chapter VIII Diseases of the ear and mastoid process	0.000	0.996	0.004
E24.0 Pituitary-dependent Cushing's disease	0.004	0.996	0.000
E22.2 Syndrome of inappropriate secretion of antidiuretic hormone	0.004	0.996	0.000
G82.4 Spastic tetraplegia	0.004	0.996	0.000
Z96.1 Presence of intraocular lens	0.000	0.996	0.004
E22 Hyperfunction of pituitary gland	0.004	0.996	0.000
H74.3 Other acquired abnormalities of ear ossicles	0.000	0.996	0.004
D52.8 Other folate deficiency anaemias	0.004	0.996	0.000
D52.1 Drug-induced folate deficiency anaemia	0.004	0.996	0.000
D52.0 Dietary folate deficiency anaemia	0.004	0.996	0.000
E23.0 Hypopituitarism	0.004	0.996	0.000
E83.1 Disorders of iron metabolism	0.000	0.996	0.004
G83.8 Other specified paralytic syndromes	0.004	0.996	0.000
H66.4 Suppurative otitis media, unspecified	0.000	0.996	0.004
E23.2 Diabetes insipidus	0.004	0.996	0.000
H74 Other disorders of middle ear and mastoid	0.000	0.996	0.004
H72.1 Attic perforation of tympanic membrane	0.000	0.996	0.004
G82.3 Flaccid tetraplegia	0.003	0.996	0.000
G82.0 Flaccid paraplegia	0.003	0.996	0.000
G83.4 Cauda equina syndrome	0.004	0.996	0.000
E20 Hypoparathyroidism	0.004	0.996	0.000
E83.3 Disorders of phosphorus metabolism	0.000	0.996	0.004
G83 Other paralytic syndromes	0.004	0.996	0.000
H74.1 Adhesive middle ear disease	0.000	0.996	0.003
E24.9 Cushing's syndrome, unspecified	0.003	0.996	0.000
K90 Intestinal malabsorption	0.000	0.996	0.004
K90.8 Other intestinal malabsorption	0.000	0.997	0.003
H72.0 Central perforation of tympanic membrane	0.000	0.997	0.003
E35 Disorders of endocrine glands in diseases classified elsewhere	0.003	0.997	0.000
E32 Diseases of thymus	0.003	0.997	0.000
E31 Polyglandular dysfunction	0.003	0.997	0.000
E30 Disorders of puberty, not elsewhere classified	0.003	0.997	0.000
E25 Adrenogenital disorders	0.003	0.997	0.000
E24.2 Drug-induced Cushing's syndrome	0.003	0.997	0.000
H66.2 Chronic atticoantral suppurative otitis media	0.000	0.997	0.003
O26.9 Pregnancy-related condition, unspecified	0.003	0.997	0.000
E24.8 Other Cushing's syndrome	0.003	0.997	0.000
E24.4 Alcohol-induced pseudo-Cushing's syndrome	0.003	0.997	0.000
E24.3 Ectopic ACTH syndrome	0.003	0.997	0.000
E24.1 Nelson's syndrome	0.003	0.997	0.000
G82.2 Paraplegia, unspecified	0.003	0.997	0.000
H74.2 Discontinuity and dislocation of ear ossicles	0.000	0.997	0.003
H75 Other disorders of middle ear and mastoid in diseases classified elsewhere	0.000	0.997	0.003
H68 Eustachian salpingitis and obstruction	0.000	0.997	0.003
H67 Otitis media in diseases classified elsewhere	0.000	0.997	0.003
E23.3 Hypothalamic dysfunction, not elsewhere classified	0.003	0.997	0.000
E23.1 Drug-induced hypopituitarism	0.003	0.997	0.000
E23.6 Other disorders of pituitary gland	0.003	0.997	0.000
H70 Mastoiditis and related conditions	0.000	0.997	0.003
E26 Hyperaldosteronism	0.003	0.997	0.000
H73 Other disorders of tympanic membrane	0.000	0.997	0.003
H72.8 Other perforations of tympanic membrane	0.000	0.997	0.003
H71 Cholesteatoma of middle ear	0.000	0.997	0.003
S06.6 Traumatic subarachnoid haemorrhage	0.000	0.997	0.003
E22.1 Hyperprolactinaemia	0.003	0.997	0.000
H66.1 Chronic tubotympanic suppurative otitis media	0.000	0.997	0.003
K90.4 Malabsorption due to intolerance, not elsewhere classified	0.000	0.997	0.003
E22.9 Hyperfunction of pituitary gland, unspecified	0.003	0.997	0.000
E22.8 Other hyperfunction of pituitary gland	0.003	0.997	0.000
E23.7 Disorder of pituitary gland, unspecified	0.003	0.997	0.000
E20.9 Hypoparathyroidism, unspecified	0.003	0.997	0.000
H66.0 Acute suppurative otitis media	0.000	0.997	0.003
M34.9 Systemic sclerosis, unspecified	0.003	0.997	0.000
K80.5 Calculus of bile duct without cholangitis or cholecystitis	0.003	0.997	0.000
M71.26 Synovial cyst of popliteal space [Baker]-Lower Leg	0.000	0.997	0.003
Z91.5 Personal history of self-harm	0.003	0.997	0.000
E29 Testicular dysfunction	0.003	0.997	0.000
H70.9 Mastoiditis, unspecified	0.000	0.997	0.003
K90.9 Intestinal malabsorption, unspecified	0.000	0.997	0.003
G80-G83 Cerebral palsy and other paralytic syndromes	0.003	0.997	0.000
E20.8 Other hypoparathyroidism	0.003	0.997	0.000
E20.1 Pseudohypoparathyroidism	0.003	0.997	0.000
E20.0 Idiopathic hypoparathyroidism	0.003	0.997	0.000
G83.5 Locked-in syndrome	0.003	0.997	0.000
G83.3 Monoplegia, unspecified	0.003	0.997	0.000
G83.0 Diplegia of upper limbs	0.003	0.997	0.000
G83.9 Paralytic syndrome, unspecified	0.003	0.997	0.000
G83.2 Monoplegia of upper limb	0.003	0.997	0.000
H72.2 Other marginal perforations of tympanic membrane	0.000	0.997	0.003
K90.3 Pancreatic steatorrhoea	0.000	0.997	0.003
K90.2 Blind loop syndrome, not elsewhere classified	0.000	0.997	0.003
K90.1 Tropical sprue	0.000	0.997	0.003
M13.90 Arthritis, unspecified (Multiple sites)	0.003	0.997	0.000
E25.9 Adrenogenital disorder, unspecified	0.002	0.997	0.000
E25.8 Other adrenogenital disorders	0.002	0.997	0.000
E25.0 Congenital adrenogenital disorders associated with enzyme deficiency	0.002	0.997	0.000
E30.9 Disorder of puberty, unspecified	0.002	0.997	0.000
E30.8 Other disorders of puberty	0.002	0.997	0.000
E30.1 Precocious puberty	0.002	0.997	0.000
E30.0 Delayed puberty	0.002	0.997	0.000
E31.9 Polyglandular dysfunction, unspecified	0.002	0.997	0.000
E31.8 Other polyglandular dysfunction	0.002	0.997	0.000
E31.1 Polyglandular hyperfunction	0.002	0.997	0.000
E31.0 Autoimmune polyglandular failure	0.002	0.997	0.000
E32.9 Disease of thymus, unspecified	0.002	0.997	0.000
E32.8 Other diseases of thymus	0.002	0.997	0.000
E32.1 Abscess of thymus	0.002	0.997	0.000
E32.0 Persistent hyperplasia of thymus	0.002	0.997	0.000
E35.8 Disorders of other endocrine glands in diseases classified elsewhere	0.002	0.997	0.000
E35.1 Disorders of adrenal glands in diseases classified elsewhere	0.002	0.997	0.000
E35.0 Disorders of thyroid gland in diseases classified elsewhere	0.002	0.997	0.000
R63.1 Polydipsia	0.003	0.997	0.000
H67.8 Otitis media in other diseases classified elsewhere	0.000	0.997	0.002
H67.1 Otitis media in viral diseases classified elsewhere	0.000	0.997	0.002
H67.0 Otitis media in bacterial diseases classified elsewhere	0.000	0.997	0.002
H68.1 Obstruction of Eustachian tube	0.000	0.997	0.002
H68.0 Eustachian salpingitis	0.000	0.997	0.002
H75.8 Other specified disorders of middle ear and mastoid in diseases classified elsewhere	0.000	0.997	0.002
H75.0 Mastoiditis in infectious and parasitic diseases classified elsewhere	0.000	0.997	0.002
H70.8 Other mastoiditis and related conditions	0.000	0.997	0.002
H70.2 Petrositis	0.000	0.997	0.002
H70.0 Acute mastoiditis	0.000	0.997	0.002
M34.1 CR(E)ST syndrome	0.003	0.997	0.000
E26.9 Hyperaldosteronism, unspecified	0.002	0.997	0.000
E26.8 Other hyperaldosteronism	0.002	0.997	0.000
E26.1 Secondary hyperaldosteronism	0.002	0.997	0.000
H74.8 Other specified disorders of middle ear and mastoid	0.000	0.997	0.002
H73.1 Chronic myringitis	0.000	0.997	0.002
H73.0 Acute myringitis	0.000	0.997	0.002
E83 Disorders of mineral metabolism	0.000	0.997	0.003
H74.0 Tympanosclerosis	0.000	0.997	0.002
H69 Other disorders of Eustachian tube	0.000	0.997	0.002
S06.61 Traumatic subarachnoid haemorrhage (with open intracranial wound)	0.000	0.997	0.002
M13.98 Arthritis, unspecified (Other)	0.003	0.997	0.000
M35.1 Other overlap syndromes	0.002	0.997	0.000
M35 Other systemic involvement of connective tissue	0.003	0.997	0.000
H73.8 Other specified disorders of tympanic membrane	0.000	0.997	0.002
H73.9 Disorder of tympanic membrane, unspecified	0.000	0.998	0.002
K25.9 Unspecified as acute or chronic, without haemorrhage or perforation	0.002	0.998	0.000
G57.6 Lesion of plantar nerve	0.000	0.998	0.002
G83.1 Monoplegia of lower limb	0.002	0.998	0.000
Q79.6 Ehlers-Danlos syndrome	0.002	0.998	0.000
E21 Hyperparathyroidism and other disorders of parathyroid gland	0.002	0.998	0.000
Q82.5 Congenital nonneoplastic naevus	0.002	0.998	0.000
Q82.8 Other specified congenital malformations of skin	0.002	0.998	0.000
E26.0 Primary hyperaldosteronism	0.002	0.998	0.000
N39.0 Urinary tract infection, site not specified	0.002	0.998	0.000
M79.69 Pain in limb (Site unspecified)	0.002	0.998	0.000
E29.9 Testicular dysfunction, unspecified	0.002	0.998	0.000
E29.8 Other testicular dysfunction	0.002	0.998	0.000
E29.0 Testicular hyperfunction	0.002	0.998	0.000
E34 Other endocrine disorders	0.002	0.998	0.000
Q82 Other congenital malformations of skin	0.002	0.998	0.000
E22.0 Acromegaly and pituitary gigantism	0.002	0.998	0.000
Q82.0 Hereditary lymphoedema	0.002	0.998	0.000
E28 Ovarian dysfunction	0.002	0.998	0.000
M35.7 Hypermobility syndrome	0.002	0.998	0.000
Y57.5 X-ray contrast media	0.002	0.998	0.000
H74.9 Disorder of middle ear and mastoid, unspecified	0.000	0.998	0.002
H74.4 Polyp of middle ear	0.000	0.998	0.002
M35.8 Other specified systemic involvement of connective tissue	0.002	0.998	0.000
M34 Systemic sclerosis	0.002	0.998	0.000
R60.9 Oedema, unspecified	0.000	0.998	0.002
E83.4 Disorders of magnesium metabolism	0.000	0.998	0.002
L30.9 Dermatitis, unspecified	0.000	0.998	0.002
G80 Infantile cerebral palsy	0.002	0.998	0.000
E21.1 Secondary hyperparathyroidism, not elsewhere classified	0.002	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.002	0.998	0.000
J01.9 Acute sinusitis, unspecified	0.000	0.998	0.002
H70.1 Chronic mastoiditis	0.000	0.998	0.002
Q79.8 Other congenital malformations of musculoskeletal system	0.002	0.998	0.000
Y57.8 Other drugs and medicaments	0.002	0.998	0.000
E83.9 Disorder of mineral metabolism, unspecified	0.000	0.998	0.002
E83.8 Other disorders of mineral metabolism	0.000	0.998	0.002
E83.2 Disorders of zinc metabolism	0.000	0.998	0.002
E83.0 Disorders of copper metabolism	0.000	0.998	0.002
H69.0 Patulous Eustachian tube	0.000	0.998	0.002
M35.9 Systemic involvement of connective tissue, unspecified	0.002	0.998	0.000
M35.6 Relapsing panniculitis [Weber-Christian]	0.002	0.998	0.000
M35.5 Multifocal fibrosclerosis	0.002	0.998	0.000
M35.4 Diffuse (eosinophilic) fasciitis	0.002	0.998	0.000
O82.0 Delivery by elective Caesarean section	0.000	0.998	0.002
H18.5 Hereditary corneal dystrophies	0.000	0.998	0.002
Q78.0 Osteogenesis imperfecta	0.002	0.998	0.000
E21.5 Disorder of parathyroid gland, unspecified	0.002	0.998	0.000
E21.4 Other specified disorders of parathyroid gland	0.002	0.998	0.000
E21.2 Other hyperparathyroidism	0.002	0.998	0.000
M35.2 Behcet's disease	0.002	0.998	0.000
H54.9 Unspecified visual impairment (binocular)	0.002	0.998	0.000
S82.10 Fracture of upper end of tibia (closed)	0.000	0.998	0.002
O43.8 Other placental disorders	0.000	0.998	0.002
C80.0 Malignant neoplasm, primary site unknown, so stated	0.002	0.998	0.000
E34.5 Androgen resistance syndrome	0.002	0.998	0.000
E34.4 Constitutional tall stature	0.002	0.998	0.000
E34.3 Short stature, not elsewhere classified	0.002	0.998	0.000
E34.2 Ectopic hormone secretion, not elsewhere classified	0.002	0.998	0.000
E34.1 Other hypersecretion of intestinal hormones	0.002	0.998	0.000
G80.8 Other infantile cerebral palsy	0.002	0.998	0.000
O47.0 False labour before 37 completed weeks of gestation	0.000	0.998	0.002
Q79.0 Congenital diaphragmatic hernia	0.002	0.998	0.000
Q82.9 Congenital malformation of skin, unspecified	0.002	0.998	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.002	0.998	0.000
Q82.3 Incontinentia pigmenti	0.002	0.998	0.000
Q82.1 Xeroderma pigmentosum	0.002	0.998	0.000
Z90.6 Acquired absence of other parts of urinary tract	0.000	0.998	0.002
E28.9 Ovarian dysfunction, unspecified	0.002	0.998	0.000
E28.8 Other ovarian dysfunction	0.002	0.998	0.000
E28.1 Androgen excess	0.002	0.998	0.000
E28.0 Oestrogen excess	0.002	0.998	0.000
M34.8 Other forms of systemic sclerosis	0.002	0.998	0.000
Q18.1 Preauricular sinus and cyst	0.002	0.998	0.000
M21.07 Valgus deformity, not elsewhere classified (Ankle and foot)	0.000	0.998	0.002
E03.2 Hypothyroidism due to medicaments and other exogenous substances	0.002	0.998	0.000
Q82.2 Mastocytosis	0.002	0.998	0.000
M34.2 Systemic sclerosis induced by drugs and chemicals	0.002	0.998	0.000
M34.0 Progressive systemic sclerosis	0.002	0.998	0.000
G80.0 Spastic cerebral palsy	0.002	0.998	0.000
L81.4 Other melanin hyperpigmentation	0.002	0.998	0.000
G80.4 Ataxic cerebral palsy	0.002	0.998	0.000
G80.3 Dyskinetic cerebral palsy	0.002	0.998	0.000
H65.2 Chronic serous otitis media	0.000	0.998	0.002
N91.2 Amenorrhoea, unspecified	0.002	0.998	0.000
O82.1 Delivery by emergency Caesarean section	0.000	0.998	0.002
H65 Nonsuppurative otitis media	0.000	0.998	0.002
H66.3 Other chronic suppurative otitis media	0.000	0.998	0.002
Q24.8 Other specified congenital malformations of heart	0.002	0.998	0.000
E03.8 Other specified hypothyroidism	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
S62.50 Fracture of thumb (closed)	0.000	0.998	0.002
E29.1 Testicular hypofunction	0.002	0.998	0.000
Y57 Other and unspecified drugs and medicaments	0.002	0.998	0.000
E34.8 Other specified endocrine disorders	0.002	0.998	0.000
F80.1 Expressive language disorder	0.000	0.998	0.002
G80.2 Infantile hemiplegia	0.002	0.998	0.000
G80.1 Spastic diplegia	0.002	0.998	0.000
Q39.4 Oesophageal web	0.002	0.998	0.000
M62.88 Other specified disorders of muscle (Other)	0.002	0.998	0.000
M35.99 Systemic involvement of connective tissue, unspecified, Site unspecified	0.002	0.998	0.000
E87.0 Hyperosmolality and hypernatraemia	0.002	0.998	0.000
G80.9 Infantile cerebral palsy, unspecified	0.002	0.998	0.000
S20.2 Contusion of thorax	0.000	0.998	0.002
E28.3 Primary ovarian failure	0.002	0.998	0.000
H69.8 Other specified disorders of Eustachian tube	0.000	0.998	0.001
C85.9 Non-Hodgkin's lymphoma, unspecified type	0.002	0.998	0.000
H69.9 Eustachian tube disorder, unspecified	0.000	0.998	0.002
Q24.5 Malformation of coronary vessels	0.002	0.998	0.000
R29.6 Tendency to fall, not elsewhere classified	0.000	0.998	0.002
Z49.0 Preparatory care for dialysis	0.000	0.998	0.002
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Y57.6 Other diagnostic agents	0.002	0.998	0.000
C85.1 B-cell lymphoma, unspecified	0.002	0.998	0.000
E34.0 Carcinoid syndrome	0.001	0.998	0.000
N85.0 Endometrial glandular hyperplasia	0.000	0.998	0.002
C71.9 Brain, unspecified	0.000	0.998	0.002
O82 Single delivery by Caesarean section	0.000	0.998	0.002
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
Q24 Other congenital malformations of heart	0.002	0.998	0.000
Q15.0 Congenital glaucoma	0.002	0.998	0.000
R63.8 Other symptoms and signs concerning food and fluid intake	0.002	0.998	0.000
Q40 Other congenital malformations of upper alimentary tract	0.002	0.998	0.000
C71.0 Cerebrum, except lobes and ventricles	0.000	0.998	0.002
E03.9 Hypothyroidism, unspecified	0.002	0.998	0.000
D04 Carcinoma in situ of skin	0.002	0.998	0.000
E21.3 Hyperparathyroidism, unspecified	0.002	0.998	0.000
E03 Other hypothyroidism	0.002	0.998	0.000
C71.3 Parietal lobe	0.000	0.998	0.002
H65.1 Other acute nonsuppurative otitis media	0.000	0.998	0.001
Q40.1 Congenital hiatus hernia	0.001	0.998	0.000
M13.94 Arthritis, unspecified (Hand)	0.002	0.998	0.000
D04.2 Skin of ear and external auricular canal	0.002	0.998	0.000
Q24.4 Congenital subaortic stenosis	0.001	0.998	0.000
N26 Unspecified contracted kidney	0.002	0.998	0.000
E34.9 Endocrine disorder, unspecified	0.001	0.998	0.000
Q15 Other congenital malformations of eye	0.001	0.998	0.000
Q24.0 Dextrocardia	0.001	0.998	0.000
Y57.7 Vitamins, not elsewhere classified	0.001	0.998	0.000
Y57.4 Pharmaceutical excipients	0.001	0.998	0.000
Y57.3 Alcohol deterrents	0.001	0.998	0.000
Y57.2 Antidotes and chelating agents, not elsewhere classified	0.001	0.998	0.000
Y57.1 Lipotropic drugs	0.001	0.998	0.000
Y57.0 Appetite depressants [anorectics]	0.001	0.998	0.000
Q39 Congenital malformations of oesophagus	0.001	0.998	0.000
M71.2 Synovial cyst of popliteal space [Baker]	0.000	0.998	0.001
X50.2 School, other institution and public administrative area	0.001	0.998	0.000
X51.9 Unspecified place	0.001	0.998	0.000
M89.09 Algoneurodystrophy (Site unspecified)	0.001	0.998	0.000
H18.9 Disorder of cornea, unspecified	0.000	0.998	0.001
S79.9 Unspecified injury of hip and thigh	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.001	0.998	0.000
M89.04 Algoneurodystrophy (Hand)	0.001	0.998	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.001	0.998	0.000
Q78.8 Other specified osteochondrodysplasias	0.001	0.998	0.000
Q78.6 Multiple congenital exostoses	0.001	0.998	0.000
Q78.5 Metaphyseal dysplasia	0.001	0.998	0.000
Q78.4 Enchondromatosis	0.001	0.998	0.000
Q78.3 Progressive diaphyseal dysplasia	0.001	0.998	0.000
Q78.2 Osteopetrosis	0.001	0.998	0.000
Q78.1 Polyostotic fibrous dysplasia	0.001	0.998	0.000
M13.92 Arthritis, unspecified (Upper arm)	0.001	0.998	0.000
H65.4 Other chronic nonsuppurative otitis media	0.000	0.998	0.001
H18.1 Bullous keratopathy	0.000	0.999	0.001
O82.8 Other single delivery by Caesarean section	0.000	0.999	0.001
O82.2 Delivery by Caesarean hysterectomy	0.000	0.999	0.001
Q18.9 Congenital malformation of face and neck, unspecified	0.001	0.999	0.000
Q18.8 Other specified congenital malformations of face and neck	0.001	0.999	0.000
Q18.7 Microcheilia	0.001	0.999	0.000
Q18.6 Macrocheilia	0.001	0.999	0.000
Q18.5 Microstomia	0.001	0.999	0.000
Q18.4 Macrostomia	0.001	0.999	0.000
Q18.3 Webbing of neck	0.001	0.999	0.000
Q18.2 Other branchial cleft malformations	0.001	0.999	0.000
Q24.6 Congenital heart block	0.001	0.999	0.000
Q24.3 Pulmonary infundibular stenosis	0.001	0.999	0.000
Q24.2 Cor triatriatum	0.001	0.999	0.000
Q24.1 Levocardia	0.001	0.999	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.001	0.999	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.001	0.999	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.001	0.999	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.001	0.999	0.000
H80-H83 Diseases of inner ear	0.000	0.999	0.001
D04.8 Skin of other sites	0.001	0.999	0.000
D04.0 Skin of lip	0.001	0.999	0.000
H65.0 Acute serous otitis media	0.000	0.999	0.001
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	0.999	0.001
C85 Other and unspecified types of non-Hodgkin's lymphoma	0.001	0.999	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.001	0.999	0.000
E03.5 Myxoedema coma	0.001	0.999	0.000
E03.4 Atrophy of thyroid (acquired)	0.001	0.999	0.000
E03.3 Postinfectious hypothyroidism	0.001	0.999	0.000
E03.1 Congenital hypothyroidism without goitre	0.001	0.999	0.000
E03.0 Congenital hypothyroidism with diffuse goitre	0.001	0.999	0.000
H18.6 Keratoconus	0.000	0.999	0.001
H40.2 Primary angle-closure glaucoma	0.000	0.999	0.001
Q44.6 Cystic disease of liver	0.001	0.999	0.000
H18 Other disorders of cornea	0.000	0.999	0.001
D04.4 Skin of scalp and neck	0.001	0.999	0.000
K76.8 Other specified diseases of liver	0.001	0.999	0.000
Q15.9 Congenital malformation of eye, unspecified	0.001	0.999	0.000
Q15.8 Other specified congenital malformations of eye	0.001	0.999	0.000
Q40.2 Other specified congenital malformations of stomach	0.001	0.999	0.000
X50.4 Street and highway	0.001	0.999	0.000
Q12 Congenital lens malformations	0.001	0.999	0.000
F79.9 Unspecified mental retardation (Without mention of impairment of behaviour)	0.001	0.999	0.000
M13.9 Arthritis, unspecified	0.001	0.999	0.000
M89.0 Algoneurodystrophy	0.001	0.999	0.000
Q18.0 Sinus, fistula and cyst of branchial cleft	0.001	0.999	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.001	0.999	0.000
Q39.8 Other congenital malformations of oesophagus	0.001	0.999	0.000
Q39.5 Congenital dilatation of oesophagus	0.001	0.999	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.001	0.999	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.001	0.999	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.001	0.999	0.000
Q39.0 Atresia of oesophagus without fistula	0.001	0.999	0.000
M71.29 Synovial cyst of popliteal space [Baker]-Site unspec	0.000	0.999	0.001
M71.28 Synovial cyst of popliteal space [Baker]-Other	0.000	0.999	0.001
M71.27 Synovial cyst of popliteal space [Baker]-Ankle/Foot	0.000	0.999	0.001
M71.25 Synovial cyst of popliteal space [Baker]-Pelvic/Thigh	0.000	0.999	0.001
M71.24 Synovial cyst of popliteal space [Baker]-Hand	0.000	0.999	0.001
M71.23 Synovial cyst of popliteal space [Baker]-Forearm	0.000	0.999	0.001
M71.22 Synovial cyst of popliteal space [Baker]-Upper arm	0.000	0.999	0.001
M71.21 Synovial cyst of popliteal space [Baker]-Shldr region	0.000	0.999	0.001
M71.20 Synovial cyst of popliteal space [Baker]-Mult sites	0.000	0.999	0.001
C43.4 Malignant melanoma of scalp and neck	0.000	0.999	0.001
D04.9 Skin, unspecified	0.001	0.999	0.000
D04.1 Skin of eyelid, including canthus	0.001	0.999	0.000
D22.6 Melanocytic naevi of upper limb, including shoulder	0.001	0.999	0.000
C71 Malignant neoplasm of brain	0.000	0.999	0.001
M87.20 Osteonecrosis due to previous trauma (Multiple sites)	0.001	0.999	0.000
Q16 Congenital malformations of ear causing impairment of hearing	0.001	0.999	0.000
Q14 Congenital malformations of posterior segment of eye	0.001	0.999	0.000
Q13 Congenital malformations of anterior segment of eye	0.001	0.999	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.001	0.999	0.000
Q45 Other congenital malformations of digestive system	0.001	0.999	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.001	0.999	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.001	0.999	0.000
X50 Overexertion and strenuous or repetitive movements	0.001	0.999	0.000
Q80-Q89 Other congenital malformations	0.001	0.999	0.000
G61.8 Other inflammatory polyneuropathies	0.001	0.999	0.000
K05.6 Periodontal disease, unspecified	0.000	0.999	0.001
Y41.8 Other specified systemic anti-infectives and antiparasitics	0.001	0.999	0.000
C85.2 Mediastinal (thymic) large B-cell lymphoma	0.001	0.999	0.000
Q44.7 Other congenital malformations of liver	0.001	0.999	0.000
Q44.5 Other congenital malformations of bile ducts	0.001	0.999	0.000
Q44.4 Choledochal cyst	0.001	0.999	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.001	0.999	0.000
Q44.2 Atresia of bile ducts	0.001	0.999	0.000
Q44.1 Other congenital malformations of gallbladder	0.001	0.999	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.001	0.999	0.000
S70.1 Contusion of thigh	0.000	0.999	0.001
Y83.9 Surgical procedure, unspecified	0.000	0.999	0.001
H82 Vertiginous syndromes in diseases classified elsewhere	0.000	0.999	0.001
Q68 Other congenital musculoskeletal deformities	0.001	0.999	0.000
R54 Senility	0.001	0.999	0.000
C85.0 Lymphosarcoma	0.001	0.999	0.000
Q12.0 Congenital cataract	0.001	0.999	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.001	0.999	0.000
Q75 Other congenital malformations of skull and face bones	0.001	0.999	0.000
Q73 Reduction defects of unspecified limb	0.001	0.999	0.000
Q72 Reduction defects of lower limb	0.001	0.999	0.000
Q71 Reduction defects of upper limb	0.001	0.999	0.000
Q70 Syndactyly	0.001	0.999	0.000
Q69 Polydactyly	0.001	0.999	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.001	0.999	0.000
M13.99 Arthritis, unspecified (Site unspecified)	0.001	0.999	0.000
G31.9 Degenerative disease of nervous system, unspecified	0.000	0.999	0.001
G31.0 Circumscribed brain atrophy	0.000	0.999	0.001
H18.7 Other corneal deformities	0.000	0.999	0.001
N60.8 Other benign mammary dysplasias	0.000	0.999	0.001
O47.9 False labour, unspecified	0.000	0.999	0.001
O82.9 Delivery by Caesarean section, unspecified	0.000	0.999	0.001
X50.6 Industrial and construction area	0.001	0.999	0.000
M89.03 Algoneurodystrophy (Forearm)	0.001	0.999	0.000
S32.80 Fracture of other and unspecified parts of lumbar spine and pelvis (closed)	0.000	0.999	0.001
H18.2 Other corneal oedema	0.000	0.999	0.001
J20.9 Acute bronchitis, unspecified	0.000	0.999	0.001
L81.8 Other specified disorders of pigmentation	0.001	0.999	0.000
Q12.9 Congenital lens malformation, unspecified	0.001	0.999	0.000
Q12.8 Other congenital lens malformations	0.001	0.999	0.000
Q12.4 Spherophakia	0.001	0.999	0.000
Q12.3 Congenital aphakia	0.001	0.999	0.000
Q12.2 Coloboma of lens	0.001	0.999	0.000
Q12.1 Congenital displaced lens	0.001	0.999	0.000
Q43.1 Hirschsprung's disease	0.001	0.999	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.001	0.999	0.000
M89.08 Algoneurodystrophy (Other)	0.001	0.999	0.000
M89.05 Algoneurodystrophy (Pelvic region and thigh)	0.001	0.999	0.000
M89.02 Algoneurodystrophy (Upper arm)	0.001	0.999	0.000
M89.01 Algoneurodystrophy (Shoulder region)	0.001	0.999	0.000
M89.00 Algoneurodystrophy (Multiple sites)	0.001	0.999	0.000
M89.55 Osteolysis (Pelvic region and thigh)	0.001	0.999	0.000
C71.7 Brain stem	0.000	0.999	0.001
C71.6 Cerebellum	0.000	0.999	0.001
C71.5 Cerebral ventricle	0.000	0.999	0.001
G24.9 Dystonia, unspecified	0.001	0.999	0.000
O81.4 Vacuum extractor delivery	0.000	0.999	0.001
Q60 Renal agenesis and other reduction defects of kidney	0.001	0.999	0.000
F33.9 Recurrent depressive disorder, unspecified	0.001	0.999	0.000
H18.3 Changes in corneal membranes	0.000	0.999	0.001
H18.0 Corneal pigmentations and deposits	0.000	0.999	0.001
N42.2 Atrophy of prostate	0.001	0.999	0.000
Q11.3 Macrophthalmos	0.001	0.999	0.000
Q11.2 Microphthalmos	0.001	0.999	0.000
Q11.1 Other anophthalmos	0.001	0.999	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