TreeWAS – Variant ID: rs6988306

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
L90.5 Scar conditions and fibrosis of skin	0.000	0.940	0.060
R11 Nausea and vomiting	0.028	0.972	0.000
L90 Atrophic disorders of skin	0.000	0.976	0.024
L90.9 Atrophic disorder of skin, unspecified	0.000	0.982	0.018
L90.8 Other atrophic disorders of skin	0.000	0.982	0.018
L90.6 Striae atrophicae	0.000	0.982	0.018
L90.4 Acrodermatitis chronica atrophicans	0.000	0.982	0.018
L90.3 Atrophoderma of Pasini and Pierini	0.000	0.982	0.018
L90.2 Anetoderma of Jadassohn-Pellizzari	0.000	0.982	0.018
L90.1 Anetoderma of Schweninger-Buzzi	0.000	0.982	0.018
L90.0 Lichen sclerosus et atrophicus	0.000	0.983	0.017
L57.0 Actinic keratosis	0.000	0.986	0.014
L72.9 Follicular cyst of skin and subcutaneous tissue, unspecified	0.010	0.990	0.000
H21.8 Other specified disorders of iris and ciliary body	0.008	0.992	0.000
H21 Other disorders of iris and ciliary body	0.008	0.992	0.000
H21.5 Other adhesions and disruptions of iris and ciliary body	0.008	0.992	0.000
H21.1 Other vascular disorders of iris and ciliary body	0.007	0.993	0.000
M25.76 Osteophyte (Lower leg)	0.007	0.993	0.000
H21.4 Pupillary membranes	0.007	0.993	0.000
T43.0 Tricyclic and tetracyclic antidepressants	0.000	0.993	0.007
T43.5 Other and unspecified antipsychotics and neuroleptics	0.000	0.993	0.007
L57 Skin changes due to chronic exposure to nonionising radiation	0.000	0.994	0.006
T43 Poisoning by psychotropic drugs, not elsewhere classified	0.000	0.994	0.006
H21.9 Disorder of iris and ciliary body, unspecified	0.006	0.994	0.000
H21.3 Cyst of iris, ciliary body and anterior chamber	0.006	0.994	0.000
H21.2 Degeneration of iris and ciliary body	0.006	0.994	0.000
H21.0 Hyphaema	0.006	0.994	0.000
I84.5 External haemorrhoids without complication	0.000	0.994	0.006
T43.3 Phenothiazine antipsychotics and neuroleptics	0.000	0.994	0.006
H15-H22 Disorders of sclera, cornea, iris and ciliary body	0.005	0.995	0.000
T43.2 Other and unspecified antidepressants	0.000	0.995	0.005
H18 Other disorders of cornea	0.005	0.995	0.000
H16 Keratitis	0.005	0.995	0.000
L57.4 Cutis laxa senilis	0.000	0.995	0.005
H15 Disorders of sclera	0.005	0.995	0.000
L57.9 Skin changes due to chronic exposure to nonionising radiation, unspecified	0.000	0.995	0.005
L57.5 Actinic granuloma	0.000	0.995	0.005
L57.3 Poikiloderma of Civatte	0.000	0.995	0.005
L57.2 Cutis rhomboidalis nuchae	0.000	0.995	0.005
L57.1 Actinic reticuloid	0.000	0.995	0.005
T43.9 Psychotropic drug, unspecified	0.000	0.995	0.005
T43.8 Other psychotropic drugs, not elsewhere classified	0.000	0.995	0.005
T43.1 Monoamine-oxidase-inhibitor antidepressants	0.000	0.995	0.005
H18.9 Disorder of cornea, unspecified	0.005	0.995	0.000
T43.4 Butyrophenone and thioxanthene neuroleptics	0.000	0.995	0.005
R25.2 Cramp and spasm	0.000	0.995	0.005
D27 Benign neoplasm of ovary	0.005	0.995	0.000
H15.1 Episcleritis	0.004	0.995	0.000
H18.2 Other corneal oedema	0.005	0.995	0.000
H18.1 Bullous keratopathy	0.004	0.995	0.000
H16.0 Corneal ulcer	0.004	0.996	0.000
R29.8 Other and unspecified symptoms and signs involving the nervous and musculoskeletal systems	0.004	0.996	0.000
T43.6 Psychostimulants with abuse potential	0.000	0.996	0.004
H16.4 Corneal neovascularisation	0.004	0.996	0.000
H16.3 Interstitial and deep keratitis	0.004	0.996	0.000
R25.1 Tremor, unspecified	0.000	0.996	0.004
H22 Disorders of iris and ciliary body in diseases classified elsewhere	0.004	0.996	0.000
H18.6 Keratoconus	0.004	0.996	0.000
H18.0 Corneal pigmentations and deposits	0.004	0.996	0.000
R50.0 Fever with chills	0.000	0.996	0.004
M25.78 Osteophyte (Other)	0.004	0.996	0.000
H19 Disorders of sclera and cornea in diseases classified elsewhere	0.004	0.996	0.000
H18.7 Other corneal deformities	0.004	0.996	0.000
H18.3 Changes in corneal membranes	0.004	0.996	0.000
A04.5 Campylobacter enteritis	0.000	0.996	0.004
H16.8 Other keratitis	0.004	0.996	0.000
H16.2 Keratoconjunctivitis	0.004	0.996	0.000
H16.1 Other superficial keratitis without conjunctivitis	0.004	0.996	0.000
H15.9 Disorder of sclera, unspecified	0.004	0.996	0.000
H15.8 Other disorders of sclera	0.004	0.996	0.000
H15.0 Scleritis	0.004	0.996	0.000
H17 Corneal scars and opacities	0.004	0.996	0.000
L57.8 Other skin changes due to chronic exposure to nonionising radiation	0.000	0.996	0.004
N60.3 Fibrosclerosis of breast	0.000	0.996	0.004
H16.9 Keratitis, unspecified	0.003	0.996	0.000
H18.4 Corneal degeneration	0.003	0.996	0.000
N70.1 Chronic salpingitis and oophoritis	0.000	0.997	0.003
N71.9 Inflammatory disease of uterus, unspecified	0.003	0.997	0.000
Y40.0 Penicillins	0.003	0.997	0.000
R25 Abnormal involuntary movements	0.000	0.997	0.003
H22.8 Other disorders of iris and ciliary body in diseases classified elsewhere	0.003	0.997	0.000
H22.1 Iridocyclitis in other diseases classified elsewhere	0.003	0.997	0.000
H22.0 Iridocyclitis in infectious and parasitic diseases classified elsewhere	0.003	0.997	0.000
H19.3 Keratitis and keratoconjunctivitis in other diseases classified elsewhere	0.003	0.997	0.000
H19.8 Other disorders of sclera and cornea in diseases classified elsewhere	0.003	0.997	0.000
H19.2 Keratitis and keratoconjunctivitis in other infectious and parasitic diseases classified elsewhere	0.003	0.997	0.000
H19.0 Scleritis and episcleritis in diseases classified elsewhere	0.003	0.997	0.000
Q27.3 Peripheral arteriovenous malformation	0.003	0.997	0.000
M25.7 Osteophyte	0.003	0.997	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.003	0.997	0.000
J94.8 Other specified pleural conditions	0.000	0.997	0.003
H18.8 Other specified disorders of cornea	0.003	0.997	0.000
M25.72 Osteophyte (Upper arm)	0.003	0.997	0.000
Y79.2 Prosthetic and other implants, materials and accessory devices	0.003	0.997	0.000
L55-L59 Radiation-related disorders of the skin and subcutaneous tissue	0.000	0.997	0.003
H17.1 Other central corneal opacity	0.003	0.997	0.000
H17.0 Adherent leukoma	0.003	0.997	0.000
T93.2 Sequelae of other fractures of lower limb	0.000	0.997	0.003
H18.5 Hereditary corneal dystrophies	0.003	0.997	0.000
Q27 Other congenital malformations of peripheral vascular system	0.003	0.997	0.000
H19.1 Herpesviral keratitis and keratoconjunctivitis	0.003	0.997	0.000
H17.8 Other corneal scars and opacities	0.003	0.997	0.000
N60.2 Fibroadenosis of breast	0.000	0.997	0.003
N71 Inflammatory disease of uterus, except cervix	0.003	0.997	0.000
N75.1 Abscess of Bartholin's gland	0.003	0.997	0.000
R06.5 Mouth breathing	0.000	0.997	0.003
M25.73 Osteophyte (Forearm)	0.003	0.997	0.000
R25.0 Abnormal head movements	0.000	0.997	0.002
N72 Inflammatory disease of cervix uteri	0.003	0.997	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.003	0.997	0.000
H17.9 Corneal scar and opacity, unspecified	0.002	0.997	0.000
H20 Iridocyclitis	0.002	0.997	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
Q12.0 Congenital cataract	0.002	0.997	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.002	0.997	0.000
M25.79 Osteophyte (Site unspecified)	0.002	0.997	0.000
M25.70 Osteophyte (Multiple sites)	0.002	0.997	0.000
S42.10 Fracture of scapula (closed)	0.002	0.997	0.000
L56 Other acute skin changes due to ultraviolet radiation	0.000	0.998	0.002
Q12 Congenital lens malformations	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
N76.2 Acute vulvitis	0.002	0.998	0.000
D38.1 Trachea, bronchus and lung	0.002	0.998	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.002	0.998	0.000
T93.3 Sequelae of dislocation, sprain and strain of lower limb	0.000	0.998	0.002
L59 Other disorders of skin and subcutaneous tissue related to radiation	0.000	0.998	0.002
L58 Radiodermatitis	0.000	0.998	0.002
L55 Sunburn	0.000	0.998	0.002
M72.27 Plantar fascial fibromatosis-Ankle/Foot	0.000	0.998	0.002
L27.1 Localised skin eruption due to drugs and medicaments	0.002	0.998	0.000
Q18.0 Sinus, fistula and cyst of branchial cleft	0.002	0.998	0.000
T46.6 Antihyperlipidaemic and antiarteriosclerotic drugs	0.000	0.998	0.002
N71.0 Acute inflammatory disease of uterus	0.002	0.998	0.000
S30.2 Contusion of external genital organs	0.002	0.998	0.000
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
N76.8 Other specified inflammation of vagina and vulva	0.002	0.998	0.000
Q27.4 Congenital phlebectasia	0.002	0.998	0.000
Q27.2 Other congenital malformations of renal artery	0.002	0.998	0.000
Q27.1 Congenital renal artery stenosis	0.002	0.998	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.002	0.998	0.000
N99.8 Other postprocedural disorders of genito-urinary system	0.000	0.998	0.002
R25.3 Fasciculation	0.000	0.998	0.002
C22.1 Intrahepatic bile duct carcinoma	0.002	0.998	0.000
H20.1 Chronic iridocyclitis	0.002	0.998	0.000
K65.0 Acute peritonitis	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
N76 Other inflammation of vagina and vulva	0.002	0.998	0.000
T93 Sequelae of injuries of lower limb	0.000	0.998	0.002
N71.1 Chronic inflammatory disease of uterus	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
N75 Diseases of Bartholin's gland	0.002	0.998	0.000
T93.1 Sequelae of fracture of femur	0.000	0.998	0.002
C22.0 Liver cell carcinoma	0.002	0.998	0.000
S30.9 Superficial injury of abdomen, lower back and pelvis, part unspecified	0.002	0.998	0.000
T42.6 Other antiepileptic and sedative-hypnotic drugs	0.000	0.998	0.002
E89.2 Postprocedural hypoparathyroidism	0.002	0.998	0.000
N76.5 Ulceration of vagina	0.002	0.998	0.000
T46 Poisoning by agents primarily affecting the cardiovascular system	0.000	0.998	0.002
M65.34 Trigger finger-Hand	0.002	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.002	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.002	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.002	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.002	0.998	0.000
Q98.5 Karyotype 47,XYY	0.002	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.002	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.002	0.998	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.002	0.998	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.002	0.998	0.000
J03.9 Acute tonsillitis, unspecified	0.002	0.998	0.000
Q21.0 Ventricular septal defect	0.002	0.998	0.000
Y79 Orthopaedic devices associated with adverse incidents	0.002	0.998	0.000
H20.2 Lens-induced iridocyclitis	0.002	0.998	0.000
Q25 Congenital malformations of great arteries	0.002	0.998	0.000
F33.9 Recurrent depressive disorder, unspecified	0.000	0.998	0.002
Z32.1 Pregnancy confirmed	0.000	0.998	0.002
L56.8 Other specified acute skin changes due to ultraviolet radiation	0.000	0.998	0.002
N76.6 Ulceration of vulva	0.002	0.998	0.000
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
M77.12 Lateral epicondylitis (Upper arm)	0.002	0.998	0.000
M50.0 Cervical disk disorder with myelopathy	0.000	0.998	0.002
Q28.2 Arteriovenous malformation of cerebral vessels	0.002	0.998	0.000
N70-N77 Inflammatory diseases of female pelvic organs	0.002	0.998	0.000
H54.7 Unspecified visual loss	0.000	0.998	0.002
N70 Salpingitis and oophoritis	0.001	0.998	0.001
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
M25.71 Osteophyte (Shoulder region)	0.002	0.998	0.000
L56.4 Polymorphous light eruption	0.000	0.998	0.002
L56.3 Solar urticaria	0.000	0.998	0.002
L56.2 Photocontact dermatitis [berloque dermatitis]	0.000	0.998	0.002
L56.1 Drug photoallergic response	0.000	0.998	0.002
L56.0 Drug phototoxic response	0.000	0.998	0.002
L56.9 Acute skin change due to ultraviolet radiation, unspecified	0.000	0.998	0.002
Q12.9 Congenital lens malformation, unspecified	0.002	0.998	0.000
Q12.8 Other congenital lens malformations	0.002	0.998	0.000
Q12.4 Spherophakia	0.002	0.998	0.000
Q12.3 Congenital aphakia	0.002	0.998	0.000
Q12.2 Coloboma of lens	0.002	0.998	0.000
Q12.1 Congenital displaced lens	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
Q24 Other congenital malformations of heart	0.002	0.998	0.000
E66.2 Extreme obesity with alveolar hypoventilation	0.002	0.998	0.000
L55.9 Sunburn, unspecified	0.000	0.998	0.002
L55.8 Other sunburn	0.000	0.998	0.002
L55.2 Sunburn of third degree	0.000	0.998	0.002
L55.1 Sunburn of second degree	0.000	0.998	0.002
L55.0 Sunburn of first degree	0.000	0.998	0.002
L58.9 Radiodermatitis, unspecified	0.000	0.998	0.002
L58.1 Chronic radiodermatitis	0.000	0.998	0.002
L58.0 Acute radiodermatitis	0.000	0.998	0.002
L59.9 Disorder of skin and subcutaneous tissue related to radiation, unspecified	0.000	0.998	0.002
L59.8 Other specified disorders of skin and subcutaneous tissue related to radiation	0.000	0.998	0.002
L59.0 Erythema ab igne [dermatitis ab igne]	0.000	0.998	0.002
N86 Erosion and ectropion of cervix uteri	0.000	0.998	0.002
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
T46.4 Angiotensin-converting-enzyme inhibitors	0.000	0.998	0.002
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
N76.1 Subacute and chronic vaginitis	0.002	0.998	0.000
T93.8 Sequelae of other specified injuries of lower limb	0.000	0.998	0.002
T42 Poisoning by antiepileptic, sedative-hypnotic and anti-Parkinsonism drugs	0.000	0.998	0.002
T42.1 Iminostilbenes	0.000	0.998	0.002
Q99 Other chromosome abnormalities, not elsewhere classified	0.002	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.002	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.002	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.002	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.002	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.002	0.998	0.000
Q90 Down's syndrome	0.002	0.998	0.000
Q18.1 Preauricular sinus and cyst	0.002	0.998	0.000
T93.6 Sequelae of crushing injury and traumatic amputation of lower limb	0.000	0.998	0.002
T93.4 Sequelae of injury of nerve of lower limb	0.000	0.998	0.002
Q96 Turner's syndrome	0.002	0.998	0.000
S30 Superficial injury of abdomen, lower back and pelvis	0.002	0.998	0.000
N75.9 Disease of Bartholin's gland, unspecified	0.002	0.998	0.000
N75.8 Other diseases of Bartholin's gland	0.002	0.998	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.002	0.998	0.000
Q21.8 Other congenital malformations of cardiac septa	0.002	0.998	0.000
Q21.4 Aortopulmonary septal defect	0.002	0.998	0.000
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
Q21.2 Atrioventricular septal defect	0.002	0.998	0.000
Q28.9 Congenital malformation of circulatory system, unspecified	0.002	0.998	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.002	0.998	0.000
Q28.3 Other malformations of cerebral vessels	0.002	0.998	0.000
Q28.1 Other malformations of precerebral vessels	0.002	0.998	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.002	0.998	0.000
S91.3 Open wound of other parts of foot	0.000	0.998	0.002
H55 Nystagmus and other irregular eye movements	0.002	0.998	0.000
F06.7 Mild cognitive disorder	0.000	0.998	0.002
T93.0 Sequelae of open wound of lower limb	0.000	0.998	0.002
T36-T50 Poisoning by drugs, medicaments and biological substances	0.000	0.998	0.002
Y81.2 Prosthetic and other implants, materials and accessory devices	0.002	0.998	0.000
Q89 Other congenital malformations, not elsewhere classified	0.002	0.998	0.000
Q17.5 Prominent ear	0.002	0.998	0.000
S30.1 Contusion of abdominal wall	0.002	0.998	0.000
N60 Benign mammary dysplasia	0.000	0.998	0.002
Q23 Congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
H20.8 Other iridocyclitis	0.002	0.998	0.000
T46.9 Other and unspecified agents primarily affecting the cardiovascular system	0.000	0.998	0.002
T46.8 Antivaricose drugs, including sclerosing agents	0.000	0.998	0.002
T46.7 Peripheral vasodilators	0.000	0.998	0.002
T46.5 Other antihypertensive drugs, not elsewhere classified	0.000	0.998	0.002
T46.3 Coronary vasodilators, not elsewhere classified	0.000	0.998	0.002
T46.2 Other antidysrhythmic drugs, not elsewhere classified	0.000	0.998	0.002
T46.0 Cardiac-stimulant glycosides and drugs of similar action	0.000	0.998	0.002
Z03.1 Observation for suspected malignant neoplasm	0.002	0.998	0.000
Q83 Congenital malformations of breast	0.002	0.998	0.000
M19.96 Arthrosis, unspecified-Lower leg	0.002	0.998	0.000
Q25.1 Coarctation of aorta	0.002	0.998	0.000
Q83.3 Accessory nipple	0.002	0.998	0.000
T46.1 Calcium-channel blockers	0.000	0.998	0.002
T93.9 Sequelae of unspecified injury of lower limb	0.000	0.998	0.002
Y79.8 Miscellaneous devices, not elsewhere classified	0.002	0.998	0.000
Y79.3 Surgical instruments, materials and devices (including sutures)	0.002	0.998	0.000
Y79.1 Therapeutic (nonsurgical) and rehabilitative devices	0.002	0.998	0.000
Y79.0 Diagnostic and monitoring devices	0.002	0.998	0.000
A04 Other bacterial intestinal infections	0.000	0.998	0.002
Q25.9 Congenital malformation of great arteries, unspecified	0.002	0.998	0.000
Q25.8 Other congenital malformations of great arteries	0.002	0.998	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.002	0.998	0.000
Q25.6 Stenosis of pulmonary artery	0.002	0.998	0.000
Q25.5 Atresia of pulmonary artery	0.002	0.998	0.000
Q25.4 Other congenital malformations of aorta	0.002	0.998	0.000
Q25.3 Stenosis of aorta	0.002	0.998	0.000
Q25.2 Atresia of aorta	0.002	0.998	0.000
Q25.0 Patent ductus arteriosus	0.002	0.998	0.000
R25.8 Other and unspecified abnormal involuntary movements	0.000	0.998	0.002
Q89.2 Congenital malformations of other endocrine glands	0.002	0.998	0.000
H20.0 Acute and subacute iridocyclitis	0.001	0.998	0.000
Q17.9 Congenital malformation of ear, unspecified	0.002	0.998	0.000
Q17.8 Other specified congenital malformations of ear	0.002	0.998	0.000
Q17.4 Misplaced ear	0.002	0.998	0.000
Q17.3 Other misshapen ear	0.002	0.998	0.000
Q17.2 Microtia	0.002	0.998	0.000
Q17.1 Macrotia	0.002	0.998	0.000
Q17.0 Accessory auricle	0.002	0.998	0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.002	0.998	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
Q20.6 Isomerism of atrial appendages	0.002	0.998	0.000
Q20.5 Discordant atrioventricular connexion	0.002	0.998	0.000
Q20.4 Double inlet ventricle	0.002	0.998	0.000
Q20.3 Discordant ventriculoarterial connexion	0.002	0.998	0.000
Q20.2 Double outlet left ventricle	0.002	0.998	0.000
Q20.1 Double outlet right ventricle	0.002	0.998	0.000
Q20.0 Common arterial trunk	0.002	0.998	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.002	0.998	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.002	0.998	0.000
Q22.6 Hypoplastic right heart syndrome	0.002	0.998	0.000
Q22.5 Ebstein's anomaly	0.002	0.998	0.000
Q22.4 Congenital tricuspid stenosis	0.002	0.998	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.002	0.998	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.002	0.998	0.000
Q22.1 Congenital pulmonary valve stenosis	0.002	0.998	0.000
Q22.0 Pulmonary valve atresia	0.002	0.998	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.002	0.998	0.000
Q26.8 Other congenital malformations of great veins	0.002	0.998	0.000
Q26.6 Portal vein-hepatic artery fistula	0.002	0.998	0.000
Q26.5 Anomalous portal venous connexion	0.002	0.998	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.002	0.998	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.002	0.998	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.002	0.998	0.000
Q26.1 Persistent left superior vena cava	0.002	0.998	0.000
Q26.0 Congenital stenosis of vena cava	0.002	0.998	0.000
N70.0 Acute salpingitis and oophoritis	0.001	0.998	0.001
N76.3 Subacute and chronic vulvitis	0.002	0.998	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.002	0.998	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.002	0.998	0.000
N74 Female pelvic inflammatory disorders in diseases classified elsewhere	0.002	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.002	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.998	0.000
Q21.1 Atrial septal defect	0.002	0.998	0.000
Q55 Other congenital malformations of male genital organs	0.002	0.998	0.000
T50 Poisoning by diuretics and other and unspecified drugs, medicaments and biological substances	0.000	0.998	0.002
Q24.6 Congenital heart block	0.002	0.998	0.000
Q24.5 Malformation of coronary vessels	0.002	0.998	0.000
Q24.4 Congenital subaortic stenosis	0.002	0.998	0.000
Q24.3 Pulmonary infundibular stenosis	0.002	0.998	0.000
Q24.2 Cor triatriatum	0.002	0.998	0.000
Q24.1 Levocardia	0.002	0.998	0.000
Q24.0 Dextrocardia	0.002	0.998	0.000
Q65.8 Other congenital deformities of hip	0.002	0.998	0.000
T93.5 Sequelae of injury of muscle and tendon of lower limb	0.000	0.998	0.002
K57.1 Diverticular disease of small intestine without perforation or abscess	0.002	0.998	0.000
Q10.7 Congenital malformation of orbit	0.001	0.998	0.000
Q10.6 Other congenital malformations of lachrymal apparatus	0.001	0.998	0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct	0.001	0.998	0.000
Q10.4 Absence and agenesis of lachrymal apparatus	0.001	0.998	0.000
Q10.3 Other congenital malformations of eyelid	0.001	0.998	0.000
Q10.2 Congenital entropion	0.001	0.998	0.000
Q10.1 Congenital ectropion	0.001	0.998	0.000
Q10.0 Congenital ptosis	0.001	0.998	0.000
Q11.3 Macrophthalmos	0.001	0.998	0.000
Q11.2 Microphthalmos	0.001	0.998	0.000
Q11.1 Other anophthalmos	0.001	0.998	0.000
Q11.0 Cystic eyeball	0.001	0.998	0.000
Q13.9 Congenital malformation of anterior segment of eye, unspecified	0.001	0.998	0.000
Q13.8 Other congenital malformations of anterior segment of eye	0.001	0.998	0.000
Q13.5 Blue sclera	0.001	0.998	0.000
Q13.4 Other congenital corneal malformations	0.001	0.998	0.000
Q13.3 Congenital corneal opacity	0.001	0.998	0.000
Q13.2 Other congenital malformations of iris	0.001	0.998	0.000
Q13.1 Absence of iris	0.001	0.998	0.000
Q13.0 Coloboma of iris	0.001	0.998	0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.001	0.998	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.001	0.998	0.000
Q14.3 Congenital malformation of choroid	0.001	0.998	0.000
Q14.2 Congenital malformation of optic disk	0.001	0.998	0.000
Q14.1 Congenital malformation of retina	0.001	0.998	0.000
Q14.0 Congenital malformation of vitreous humour	0.001	0.998	0.000
Q15.9 Congenital malformation of eye, unspecified	0.001	0.998	0.000
Q15.8 Other specified congenital malformations of eye	0.001	0.998	0.000
Q15.0 Congenital glaucoma	0.001	0.998	0.000
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified	0.001	0.998	0.000
Q16.5 Congenital malformation of inner ear	0.001	0.998	0.000
Q16.4 Other congenital malformations of middle ear	0.001	0.998	0.000
Q16.3 Congenital malformation of ear ossicles	0.001	0.998	0.000
Q16.2 Absence of eustachian tube	0.001	0.998	0.000
Q16.1 Congenital absence, atresia and stricture of auditory canal (external)	0.001	0.998	0.000
Q16.0 Congenital absence of (ear) auricle	0.001	0.998	0.000
Q85.0 Neurofibromatosis (nonmalignant)	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
M25.74 Osteophyte (Hand)	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
C22 Malignant neoplasm of liver and intrahepatic bile ducts	0.002	0.998	0.000
Q65 Congenital deformities of hip	0.002	0.998	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.002	0.998	0.000
D03.3 Melanoma in situ of other and unspecified parts of face	0.000	0.998	0.002
D37.4 Colon	0.002	0.998	0.000
T42.8 Anti-Parkinsonism drugs and other central muscle-tone depressants	0.000	0.998	0.002
T42.5 Mixed antiepileptics, not elsewhere classified	0.000	0.998	0.002
T42.3 Barbiturates	0.000	0.998	0.002
T42.2 Succinimides and oxazolidinediones	0.000	0.998	0.002
T47 Poisoning by agents primarily affecting gastro-intestinal system	0.000	0.998	0.002
Y81 General- and plastic-surgery devices associated with adverse incidents	0.002	0.998	0.000
Q50-Q56 Congenital malformations of genital organs	0.002	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
J06.9 Acute upper respiratory infection, unspecified	0.002	0.998	0.000
Q83.8 Other congenital malformations of breast	0.002	0.998	0.000
Q90.9 Down's syndrome, unspecified	0.001	0.998	0.000
Q90.2 Trisomy 21, translocation	0.001	0.998	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.001	0.998	0.000
Q91.7 Patau's syndrome, unspecified	0.001	0.998	0.000
Q91.6 Trisomy 13, translocation	0.001	0.998	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.001	0.998	0.000
Q91.3 Edwards' syndrome, unspecified	0.001	0.998	0.000
Q91.2 Trisomy 18, translocation	0.001	0.998	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.001	0.998	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.001	0.998	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.001	0.998	0.000
Q92.7 Triploidy and polyploidy	0.001	0.998	0.000
Q92.6 Extra marker chromosomes	0.001	0.998	0.000
Q92.5 Duplications with other complex rearrangements	0.001	0.998	0.000
Q92.4 Duplications seen only at prometaphase	0.001	0.998	0.000
Q92.3 Minor partial trisomy	0.001	0.998	0.000
Q92.2 Major partial trisomy	0.001	0.998	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.001	0.998	0.000
Q93.9 Deletion from autosomes, unspecified	0.001	0.998	0.000
Q93.8 Other deletions from the autosomes	0.001	0.998	0.000
Q93.7 Deletions with other complex rearrangements	0.001	0.998	0.000
Q93.6 Deletions seen only at prometaphase	0.001	0.998	0.000
Q93.5 Other deletions of part of a chromosome	0.001	0.998	0.000
Q93.4 Deletion of short arm of chromosome 5	0.001	0.998	0.000
Q93.3 Deletion of short arm of chromosome 4	0.001	0.998	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.001	0.998	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.001	0.998	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.001	0.998	0.000
Q95.8 Other balanced rearrangements and structural markers	0.001	0.998	0.000
Q95.5 Individuals with autosomal fragile site	0.001	0.998	0.000
Q95.4 Individuals with marker heterochromatin	0.001	0.998	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.001	0.998	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.001	0.998	0.000
Q95.1 Chromosome inversion in normal individual	0.001	0.998	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.001	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.001	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.001	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.001	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.001	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.001	0.998	0.000
Q96.0 Karyotype 45,X	0.001	0.998	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.001	0.998	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.001	0.998	0.000
Q97.3 Female with 46,XY karyotype	0.001	0.998	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.001	0.998	0.000
Q97.1 Female with more than three X chromosomes	0.001	0.998	0.000
Q97.0 Karyotype 47,XXX	0.001	0.998	0.000
Q99.9 Chromosomal abnormality, unspecified	0.001	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.001	0.998	0.000
Q99.2 Fragile X chromosome	0.001	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.001	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.001	0.998	0.000
S30.7 Multiple superficial injuries of abdomen, lower back and pelvis	0.002	0.998	0.000
T42.7 Antiepileptic and sedative-hypnotic drugs, unspecified	0.000	0.998	0.002
Q07 Other congenital malformations of nervous system	0.001	0.998	0.000
A04.8 Other specified bacterial intestinal infections	0.000	0.998	0.002
B34.8 Other viral infections of unspecified site	0.002	0.998	0.000
N60.0 Solitary cyst of breast	0.000	0.998	0.002
Q07.0 Arnold-Chiari syndrome	0.002	0.998	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.001	0.998	0.000
M25.75 Osteophyte (Pelvic region and thigh)	0.002	0.998	0.000
Q96.9 Turner's syndrome, unspecified	0.001	0.998	0.000
T50.9 Other and unspecified drugs, medicaments and biological substances	0.000	0.998	0.002
R29 Other symptoms and signs involving the nervous and musculoskeletal systems	0.002	0.998	0.000
T49 Poisoning by topical agents primarily affecting skin and mucous membrane and by ophthalmological, otorhinolarygological and dental drugs	0.000	0.998	0.002
T48 Poisoning by agents primarily acting on smooth and skeletal muscles and the respiratory system	0.000	0.998	0.002
T41 Poisoning by anaesthetics and therapeutic gases	0.000	0.998	0.002
N75.0 Cyst of Bartholin's gland	0.002	0.998	0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.001	0.998	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.001	0.998	0.000
Q23.4 Hypoplastic left heart syndrome	0.001	0.998	0.000
Q23.3 Congenital mitral insufficiency	0.001	0.998	0.000
Q23.2 Congenital mitral stenosis	0.001	0.998	0.000
Q55.6 Other congenital malformations of penis	0.001	0.998	0.000
Q85.1 Tuberous sclerosis	0.001	0.998	0.000
Q89.9 Congenital malformation, unspecified	0.001	0.998	0.000
Q89.8 Other specified congenital malformations	0.001	0.998	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.001	0.998	0.000
Q89.4 Conjoined twins	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