TreeWAS – Variant ID: rs2075064

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
R03.0 Elevated blood-pressure reading, without diagnosis of hypertension	0.000	0.515	0.485
R03 Abnormal blood-pressure reading, without diagnosis	0.000	0.824	0.176
R03.1 Nonspecific low blood-pressure reading	0.000	0.886	0.114
H16.0 Corneal ulcer	0.015	0.985	0.000
Q79.6 Ehlers-Danlos syndrome	0.014	0.986	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.014	0.986	0.000
Z11.2 Special screening examination for other bacterial diseases	0.013	0.987	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.012	0.988	0.000
H16 Keratitis	0.012	0.988	0.000
Q76 Congenital malformations of spine and bony thorax	0.012	0.988	0.000
Q79.8 Other congenital malformations of musculoskeletal system	0.011	0.988	0.000
H16.8 Other keratitis	0.011	0.989	0.000
Q76.0 Spina bifida occulta	0.011	0.989	0.000
Q79.0 Congenital diaphragmatic hernia	0.011	0.989	0.000
H16.9 Keratitis, unspecified	0.011	0.989	0.000
Q79.1 Other congenital malformations of diaphragm	0.010	0.989	0.000
Q65 Congenital deformities of hip	0.011	0.989	0.000
H16.1 Other superficial keratitis without conjunctivitis	0.010	0.990	0.000
Q74 Other congenital malformations of limb(s)	0.010	0.990	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.010	0.990	0.000
Q79.5 Other congenital malformations of abdominal wall	0.010	0.990	0.000
Q79.4 Prune belly syndrome	0.010	0.990	0.000
Q79.3 Gastroschisis	0.010	0.990	0.000
Q79.2 Exomphalos	0.010	0.990	0.000
Q70 Syndactyly	0.010	0.990	0.000
Q78 Other osteochondrodysplasias	0.010	0.990	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.009	0.991	0.000
D18.0 Haemangioma, any site	0.000	0.991	0.009
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.009	0.991	0.000
Q65.8 Other congenital deformities of hip	0.009	0.991	0.000
Q76.5 Cervical rib	0.009	0.991	0.000
Q76.1 Klippel-Feil syndrome	0.009	0.991	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.009	0.991	0.000
Q75 Other congenital malformations of skull and face bones	0.009	0.991	0.000
Q73 Reduction defects of unspecified limb	0.009	0.991	0.000
Q72 Reduction defects of lower limb	0.009	0.991	0.000
Q71 Reduction defects of upper limb	0.009	0.991	0.000
Q69 Polydactyly	0.009	0.991	0.000
H16.3 Interstitial and deep keratitis	0.009	0.991	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.009	0.991	0.000
Q76.8 Other congenital malformations of bony thorax	0.009	0.991	0.000
Q76.7 Congenital malformation of sternum	0.009	0.991	0.000
Q76.6 Other congenital malformations of ribs	0.009	0.991	0.000
Q76.3 Congenital scoliosis due to congenital bony malformation	0.009	0.991	0.000
Q76.2 Congenital spondylolisthesis	0.009	0.991	0.000
Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle	0.009	0.991	0.000
Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle	0.009	0.991	0.000
H16.4 Corneal neovascularisation	0.008	0.992	0.000
Q68 Other congenital musculoskeletal deformities	0.008	0.992	0.000
Q65.9 Congenital deformity of hip, unspecified	0.008	0.992	0.000
Q65.1 Congenital dislocation of hip, bilateral	0.008	0.992	0.000
Q70.3 Webbed toes	0.008	0.992	0.000
Q65.6 Unstable hip	0.008	0.992	0.000
Q65.5 Congenital subluxation of hip, unspecified	0.008	0.992	0.000
Q65.4 Congenital subluxation of hip, bilateral	0.008	0.992	0.000
Q65.3 Congenital subluxation of hip, unilateral	0.008	0.992	0.000
Q65.0 Congenital dislocation of hip, unilateral	0.008	0.992	0.000
Q78.2 Osteopetrosis	0.008	0.992	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.008	0.992	0.000
Q74.9 Unspecified congenital malformation of limb(s)	0.007	0.992	0.000
Q74.8 Other specified congenital malformations of limb(s)	0.007	0.992	0.000
Q74.3 Arthrogryposis multiplex congenita	0.007	0.992	0.000
H16.2 Keratoconjunctivitis	0.007	0.992	0.000
Q65.2 Congenital dislocation of hip, unspecified	0.007	0.993	0.000
Q70.9 Syndactyly, unspecified	0.007	0.993	0.000
Q70.4 Polysyndactyly	0.007	0.993	0.000
Q70.2 Fused toes	0.007	0.993	0.000
Q70.1 Webbed fingers	0.007	0.993	0.000
Q70.0 Fused fingers	0.007	0.993	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.007	0.993	0.000
Q78.8 Other specified osteochondrodysplasias	0.007	0.993	0.000
Q78.6 Multiple congenital exostoses	0.007	0.993	0.000
Q78.5 Metaphyseal dysplasia	0.007	0.993	0.000
Q78.4 Enchondromatosis	0.007	0.993	0.000
Q78.3 Progressive diaphyseal dysplasia	0.007	0.993	0.000
Q78.1 Polyostotic fibrous dysplasia	0.007	0.993	0.000
E80.4 Gilbert's syndrome	0.000	0.993	0.007
Q78.0 Osteogenesis imperfecta	0.007	0.993	0.000
Q87.4 Marfan's syndrome	0.007	0.993	0.000
Q67.8 Other congenital deformities of chest	0.007	0.993	0.000
Q67.7 Pectus carinatum	0.007	0.993	0.000
Q67.3 Plagiocephaly	0.007	0.993	0.000
Q67.2 Dolichocephaly	0.007	0.993	0.000
Q67.1 Compression facies	0.007	0.993	0.000
Q67.0 Facial asymmetry	0.007	0.993	0.000
Q89.2 Congenital malformations of other endocrine glands	0.007	0.993	0.000
Q66 Congenital deformities of feet	0.007	0.993	0.000
Q67.6 Pectus excavatum	0.007	0.993	0.000
Q69.9 Polydactyly, unspecified	0.007	0.993	0.000
Q69.2 Accessory toe(s)	0.007	0.993	0.000
Q69.1 Accessory thumb(s)	0.007	0.993	0.000
Q69.0 Accessory finger(s)	0.007	0.993	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.007	0.993	0.000
Q71.8 Other reduction defects of upper limb(s)	0.007	0.993	0.000
Q71.6 Lobster-claw hand	0.007	0.993	0.000
Q71.5 Longitudinal reduction defect of ulna	0.007	0.993	0.000
Q71.4 Longitudinal reduction defect of radius	0.007	0.993	0.000
Q71.3 Congenital absence of hand and finger(s)	0.007	0.993	0.000
Q71.2 Congenital absence of both forearm and hand	0.007	0.993	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.007	0.993	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.007	0.993	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.007	0.993	0.000
Q72.8 Other reduction defects of lower limb(s)	0.007	0.993	0.000
Q72.7 Split foot	0.007	0.993	0.000
Q72.6 Longitudinal reduction defect of fibula	0.007	0.993	0.000
Q72.5 Longitudinal reduction defect of tibia	0.007	0.993	0.000
Q72.4 Longitudinal reduction defect of femur	0.007	0.993	0.000
Q72.3 Congenital absence of foot and toe(s)	0.007	0.993	0.000
Q72.2 Congenital absence of both lower leg and foot	0.007	0.993	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.007	0.993	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.007	0.993	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.007	0.993	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.007	0.993	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.007	0.993	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.007	0.993	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.007	0.993	0.000
Q75.5 Oculomandibular dysostosis	0.007	0.993	0.000
Q75.4 Mandibulofacial dysostosis	0.007	0.993	0.000
Q75.3 Macrocephaly	0.007	0.993	0.000
Q75.2 Hypertelorism	0.007	0.993	0.000
Q75.1 Craniofacial dysostosis	0.007	0.993	0.000
Q75.0 Craniosynostosis	0.007	0.993	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.007	0.993	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.007	0.993	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.007	0.993	0.000
Q77.6 Chondroectodermal dysplasia	0.007	0.993	0.000
Q77.5 Diastrophic dysplasia	0.007	0.993	0.000
Q77.4 Achondroplasia	0.007	0.993	0.000
Q77.3 Chondrodysplasia punctata	0.007	0.993	0.000
Q77.2 Short rib syndrome	0.007	0.993	0.000
Q77.1 Thanatophoric short stature	0.007	0.993	0.000
Q77.0 Achondrogenesis	0.007	0.993	0.000
Q67.5 Congenital deformity of spine	0.007	0.993	0.000
Z11 Special screening examination for infectious and parasitic diseases	0.007	0.993	0.000
N80.1 Endometriosis of ovary	0.000	0.993	0.007
Q89 Other congenital malformations, not elsewhere classified	0.006	0.994	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.006	0.994	0.000
Q74.1 Congenital malformation of knee	0.006	0.994	0.000
E13.9 Without complications	0.000	0.994	0.006
Q68.5 Congenital bowing of long bones of leg, unspecified	0.006	0.994	0.000
Q68.4 Congenital bowing of tibia and fibula	0.006	0.994	0.000
Q68.3 Congenital bowing of femur	0.006	0.994	0.000
Q68.2 Congenital deformity of knee	0.006	0.994	0.000
Q68.1 Congenital deformity of hand	0.006	0.994	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.006	0.994	0.000
Z11.0 Special screening examination for intestinal infectious diseases	0.006	0.994	0.000
Q80-Q89 Other congenital malformations	0.006	0.994	0.000
H18.5 Hereditary corneal dystrophies	0.006	0.994	0.000
H15-H22 Disorders of sclera, cornea, iris and ciliary body	0.006	0.994	0.000
N64.8 Other specified disorders of breast	0.006	0.994	0.000
Z11.9 Special screening examination for infectious and parasitic diseases, unspecified	0.006	0.994	0.000
Q66.6 Other congenital valgus deformities of feet	0.006	0.994	0.000
H18.2 Other corneal oedema	0.006	0.994	0.000
H18 Other disorders of cornea	0.006	0.994	0.000
Q66.0 Talipes equinovarus	0.005	0.995	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.005	0.995	0.000
J15.4 Pneumonia due to other streptococci	0.000	0.995	0.005
Q66.7 Pes cavus	0.005	0.995	0.000
Q66.9 Congenital deformity of feet, unspecified	0.005	0.995	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.005	0.995	0.000
Z11.6 Special screening examination for other protozoal diseases and helminthiases	0.005	0.995	0.000
Q66.5 Congenital pes planus	0.005	0.995	0.000
Q66.4 Talipes calcaneovalgus	0.005	0.995	0.000
Q66.1 Talipes calcaneovarus	0.005	0.995	0.000
Z11.1 Special screening examination for respiratory tuberculosis	0.005	0.995	0.000
F20.0 Paranoid schizophrenia	0.000	0.995	0.005
C49.0 Connective and soft tissue of head, face and neck	0.005	0.995	0.000
Z11.3 Special screening examination for infections with a predominantly sexual mode of transmission	0.005	0.995	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.005	0.995	0.000
N64.9 Disorder of breast, unspecified	0.005	0.995	0.000
C49.3 Connective and soft tissue of thorax	0.005	0.995	0.000
C49.1 Connective and soft tissue of upper limb, including shoulder	0.005	0.995	0.000
Q89.3 Situs inversus	0.005	0.995	0.000
Q83 Congenital malformations of breast	0.005	0.995	0.000
H21 Other disorders of iris and ciliary body	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
Q89.9 Congenital malformation, unspecified	0.005	0.995	0.000
Q89.8 Other specified congenital malformations	0.005	0.995	0.000
Q89.7 Multiple congenital malformations, not elsewhere classified	0.005	0.995	0.000
Q89.4 Conjoined twins	0.005	0.995	0.000
Q89.1 Congenital malformations of adrenal gland	0.005	0.995	0.000
Q89.0 Congenital malformations of spleen	0.005	0.995	0.000
Q66.3 Other congenital varus deformities of feet	0.005	0.995	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.005	0.995	0.000
Z11.5 Special screening examination for other viral diseases	0.005	0.995	0.000
H19 Disorders of sclera and cornea in diseases classified elsewhere	0.005	0.995	0.000
C49 Malignant neoplasm of other connective and soft tissue	0.005	0.995	0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.005	0.995	0.000
Q84 Other congenital malformations of integument	0.005	0.995	0.000
Q81 Epidermolysis bullosa	0.005	0.995	0.000
Q80 Congenital ichthyosis	0.005	0.995	0.000
H18.7 Other corneal deformities	0.005	0.995	0.000
H18.4 Corneal degeneration	0.005	0.995	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.004	0.995	0.000
M43.06 Spondylolysis (Lumbar region)	0.005	0.995	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.004	0.995	0.000
H21.5 Other adhesions and disruptions of iris and ciliary body	0.004	0.996	0.000
H22 Disorders of iris and ciliary body in diseases classified elsewhere	0.004	0.996	0.000
H18.0 Corneal pigmentations and deposits	0.004	0.996	0.000
Q82 Other congenital malformations of skin	0.004	0.996	0.000
H21.1 Other vascular disorders of iris and ciliary body	0.004	0.996	0.000
H18.3 Changes in corneal membranes	0.004	0.996	0.000
Q66.2 Metatarsus varus	0.004	0.996	0.000
H21.2 Degeneration of iris and ciliary body	0.004	0.996	0.000
H18.9 Disorder of cornea, unspecified	0.004	0.996	0.000
Q83.3 Accessory nipple	0.004	0.996	0.000
C49.6 Connective and soft tissue of trunk, unspecified	0.004	0.996	0.000
H18.1 Bullous keratopathy	0.004	0.996	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.004	0.996	0.000
H21.9 Disorder of iris and ciliary body, unspecified	0.004	0.996	0.000
Z11.8 Special screening examination for other infectious and parasitic diseases	0.004	0.996	0.000
H15 Disorders of sclera	0.004	0.996	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.004	0.996	0.000
E13 Other specified diabetes mellitus	0.000	0.996	0.004
C49.9 Connective and soft tissue, unspecified	0.004	0.996	0.000
Q83.8 Other congenital malformations of breast	0.004	0.996	0.000
H19.2 Keratitis and keratoconjunctivitis in other infectious and parasitic diseases classified elsewhere	0.004	0.996	0.000
H19.1 Herpesviral keratitis and keratoconjunctivitis	0.004	0.996	0.000
H21.4 Pupillary membranes	0.004	0.996	0.000
Q83.9 Congenital malformation of breast, unspecified	0.004	0.996	0.000
Q83.2 Absent nipple	0.004	0.996	0.000
Q83.0 Congenital absence of breast with absent nipple	0.004	0.996	0.000
Z48.9 Surgical follow-up care, unspecified	0.004	0.996	0.000
H21.3 Cyst of iris, ciliary body and anterior chamber	0.004	0.996	0.000
Q35-Q37 Cleft lip and cleft palate	0.004	0.996	0.000
H19.8 Other disorders of sclera and cornea in diseases classified elsewhere	0.004	0.996	0.000
H19.0 Scleritis and episcleritis in diseases classified elsewhere	0.004	0.996	0.000
M47.89 Other spondylosis (Site unspecified)	0.004	0.996	0.000
H19.3 Keratitis and keratoconjunctivitis in other diseases classified elsewhere	0.004	0.996	0.000
C49.8 Overlapping lesion of connective and soft tissue	0.003	0.996	0.000
Q83.1 Accessory breast	0.003	0.996	0.000
Z11.4 Special screening examination for human immunodeficiency virus [HIV]	0.003	0.996	0.000
Q80.9 Congenital ichthyosis, unspecified	0.003	0.996	0.000
Q80.8 Other congenital ichthyosis	0.003	0.996	0.000
Q80.4 Harlequin foetus	0.003	0.996	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.003	0.996	0.000
Q80.2 Lamellar ichthyosis	0.003	0.996	0.000
Q80.1 X-linked ichthyosis	0.003	0.996	0.000
Q80.0 Ichthyosis vulgaris	0.003	0.996	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.003	0.996	0.000
Q81.8 Other epidermolysis bullosa	0.003	0.996	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.003	0.996	0.000
Q81.1 Epidermolysis bullosa letalis	0.003	0.996	0.000
Q81.0 Epidermolysis bullosa simplex	0.003	0.996	0.000
Q82.2 Mastocytosis	0.004	0.996	0.000
Q84.9 Congenital malformation of integument, unspecified	0.003	0.996	0.000
Q84.8 Other specified congenital malformations of integument	0.003	0.996	0.000
Q84.6 Other congenital malformations of nails	0.003	0.996	0.000
Q84.5 Enlarged and hypertrophic nails	0.003	0.996	0.000
Q84.4 Congenital leukonychia	0.003	0.996	0.000
Q84.3 Anonychia	0.003	0.996	0.000
Q84.2 Other congenital malformations of hair	0.003	0.996	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.003	0.996	0.000
Q84.0 Congenital alopecia	0.003	0.996	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.003	0.996	0.000
Q86.2 Dysmorphism due to warfarin	0.003	0.996	0.000
Q86.1 Foetal hydantoin syndrome	0.003	0.996	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.003	0.996	0.000
S79.9 Unspecified injury of hip and thigh	0.004	0.996	0.000
H20 Iridocyclitis	0.003	0.996	0.000
D18 Haemangioma and lymphangioma, any site	0.000	0.996	0.004
Q60-Q64 Congenital malformations of the urinary system	0.004	0.996	0.000
E13.3 With ophthalmic complications	0.000	0.996	0.003
K85.1 Biliary acute pancreatitis	0.000	0.997	0.003
Q38-Q45 Other congenital malformations of the digestive system	0.003	0.997	0.000
Q82.0 Hereditary lymphoedema	0.003	0.997	0.000
H22.8 Other disorders of iris and ciliary body in 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
Q31 Congenital malformations of larynx	0.003	0.997	0.000
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
Q66.8 Other congenital deformities of feet	0.003	0.997	0.000
H20.1 Chronic iridocyclitis	0.003	0.997	0.000
H22.1 Iridocyclitis in other diseases classified elsewhere	0.003	0.997	0.000
Q85 Phakomatoses, not elsewhere classified	0.003	0.997	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.003	0.997	0.000
Q82.9 Congenital malformation of skin, unspecified	0.003	0.997	0.000
Q82.4 Ectodermal dysplasia (anhidrotic)	0.003	0.997	0.000
Q82.3 Incontinentia pigmenti	0.003	0.997	0.000
Q82.1 Xeroderma pigmentosum	0.003	0.997	0.000
Z00.0 General medical examination	0.000	0.997	0.003
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.003	0.997	0.000
M43.0 Spondylolysis	0.003	0.997	0.000
Q30 Congenital malformations of nose	0.003	0.997	0.000
Q40 Other congenital malformations of upper alimentary tract	0.003	0.997	0.000
Q34 Other congenital malformations of respiratory system	0.003	0.997	0.000
Q33 Congenital malformations of lung	0.003	0.997	0.000
Q32 Congenital malformations of trachea and bronchus	0.003	0.997	0.000
H15.0 Scleritis	0.003	0.997	0.000
Z47.8 Other specified orthopaedic follow-up care	0.000	0.997	0.003
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.003	0.997	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.003	0.997	0.000
Q90 Down's syndrome	0.003	0.997	0.000
C49.4 Connective and soft tissue of abdomen	0.003	0.997	0.000
H15.9 Disorder of sclera, unspecified	0.003	0.997	0.000
H17 Corneal scars and opacities	0.003	0.997	0.000
E13.8 With unspecified complications	0.000	0.997	0.003
E13.7 With multiple complications	0.000	0.997	0.003
E13.6 With other specified complications	0.000	0.997	0.003
E13.5 With peripheral circulatory complications	0.000	0.997	0.003
E13.4 With neurological complications	0.000	0.997	0.003
E13.2 With renal complications	0.000	0.997	0.003
E13.1 With ketoacidosis	0.000	0.997	0.003
E13.0 With coma	0.000	0.997	0.003
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.003	0.997	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.003	0.997	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.003	0.997	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.003	0.997	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.003	0.997	0.000
H21.0 Hyphaema	0.003	0.997	0.000
N64 Other disorders of breast	0.003	0.997	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.003	0.997	0.000
C49.2 Connective and soft tissue of lower limb, including hip	0.003	0.997	0.000
Q44.6 Cystic disease of liver	0.003	0.997	0.000
Q61 Cystic kidney disease	0.003	0.997	0.000
H20.0 Acute and subacute iridocyclitis	0.003	0.997	0.000
Q96 Turner's syndrome	0.003	0.997	0.000
S22.10 Multiple fractures of thoracic spine (closed)	0.000	0.997	0.003
Q62.8 Other congenital malformations of ureter	0.003	0.997	0.000
Q37 Cleft palate with cleft lip	0.003	0.997	0.000
Q44.4 Choledochal cyst	0.003	0.997	0.000
Q36 Cleft lip	0.003	0.997	0.000
Q00-Q07 Congenital malformations of the nervous system	0.003	0.997	0.000
Q40.2 Other specified congenital malformations of stomach	0.003	0.997	0.000
H15.8 Other disorders of sclera	0.003	0.997	0.000
H15.1 Episcleritis	0.003	0.997	0.000
N85.1 Endometrial adenomatous hyperplasia	0.000	0.997	0.003
Q99.8 Other specified chromosome abnormalities	0.003	0.997	0.000
H20.2 Lens-induced iridocyclitis	0.003	0.997	0.000
Q22.5 Ebstein's anomaly	0.003	0.997	0.000
Q31.3 Laryngocele	0.003	0.997	0.000
Q31.0 Web of larynx	0.003	0.997	0.000
F20 Schizophrenia	0.000	0.997	0.003
Q61.5 Medullary cystic kidney	0.003	0.997	0.000
Q24 Other congenital malformations of heart	0.003	0.997	0.000
Q39 Congenital malformations of oesophagus	0.003	0.997	0.000
Q40.1 Congenital hiatus hernia	0.003	0.997	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.003	0.997	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.003	0.997	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.003	0.997	0.000
Q85.1 Tuberous sclerosis	0.003	0.997	0.000
Q22.1 Congenital pulmonary valve stenosis	0.003	0.997	0.000
Q61.3 Polycystic kidney, unspecified	0.003	0.997	0.000
Q62.1 Atresia and stenosis of ureter	0.003	0.997	0.000
Q82.5 Congenital nonneoplastic naevus	0.003	0.997	0.000
Q35 Cleft palate	0.002	0.997	0.000
M43.07 Spondylolysis (Lumbosacral region)	0.003	0.997	0.000
Q31.9 Congenital malformation of larynx, unspecified	0.002	0.997	0.000
Q31.8 Other congenital malformations of larynx	0.002	0.997	0.000
Q31.5 Congenital laryngomalacia	0.002	0.997	0.000
Q31.4 Congenital laryngeal stridor	0.002	0.997	0.000
Q31.2 Laryngeal hypoplasia	0.002	0.997	0.000
Q31.1 Congenital subglottic stenosis	0.002	0.997	0.000
Q28 Other congenital malformations of circulatory system	0.003	0.997	0.000
Q26 Congenital malformations of great veins	0.003	0.997	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.003	0.997	0.000
C49.5 Connective and soft tissue of pelvis	0.002	0.997	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.003	0.997	0.000
Q82.8 Other specified congenital malformations of skin	0.003	0.997	0.000
Q27 Other congenital malformations of peripheral vascular system	0.003	0.997	0.000
M43.09 Spondylolysis (Site unspecified)	0.003	0.997	0.000
M43.02 Spondylolysis (Cervical region)	0.003	0.997	0.000
Q62.2 Congenital megaloureter	0.003	0.997	0.000
Q99.9 Chromosomal abnormality, unspecified	0.002	0.997	0.000
Q99.2 Fragile X chromosome	0.002	0.997	0.000
Q99.1 46,XX true hermaphrodite	0.002	0.997	0.000
Q99.0 Chimera 46,XX/46,XY	0.002	0.997	0.000
Q50-Q56 Congenital malformations of genital organs	0.003	0.997	0.000
H11.0 Pterygium	0.003	0.997	0.000
M43.08 Spondylolysis (Sacral and sacrococcygeal region)	0.002	0.997	0.000
M43.05 Spondylolysis (Thoracolumbar region)	0.002	0.997	0.000
M43.04 Spondylolysis (Thoracic region)	0.002	0.997	0.000
M43.03 Spondylolysis (Cervicothoracic region)	0.002	0.997	0.000
M43.01 Spondylolysis (Occipito-atlanto-axial region)	0.002	0.997	0.000
M43.00 Spondylolysis (Multiple sites in spine)	0.002	0.997	0.000
Q44.7 Other congenital malformations of liver	0.002	0.997	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.002	0.997	0.000
Q44.2 Atresia of bile ducts	0.002	0.997	0.000
Q44.1 Other congenital malformations of gallbladder	0.002	0.997	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.002	0.997	0.000
D18.1 Lymphangioma, any site	0.000	0.997	0.003
N64.3 Galactorrhoea not associated with childbirth	0.003	0.997	0.000
Q61.9 Cystic kidney disease, unspecified	0.003	0.997	0.000
Q30.9 Congenital malformation of nose, unspecified	0.002	0.997	0.000
Q30.8 Other congenital malformations of nose	0.002	0.997	0.000
Q30.3 Congenital perforated nasal septum	0.002	0.997	0.000
Q30.2 Fissured, notched and cleft nose	0.002	0.997	0.000
Q30.1 Agenesis and underdevelopment of nose	0.002	0.997	0.000
Q30.0 Choanal atresia	0.002	0.997	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.997	0.000
L57.8 Other skin changes due to chronic exposure to nonionising radiation	0.003	0.997	0.000
Q28.0 Arteriovenous malformation of precerebral vessels	0.002	0.997	0.000
Q32.4 Other congenital malformations of bronchus	0.002	0.997	0.000
Q32.3 Congenital stenosis of bronchus	0.002	0.997	0.000
Q32.2 Congenital bronchomalacia	0.002	0.997	0.000
Q32.1 Other congenital malformations of trachea	0.002	0.997	0.000
Q32.0 Congenital tracheomalacia	0.002	0.997	0.000
Q33.9 Congenital malformation of lung, unspecified	0.002	0.997	0.000
Q33.8 Other congenital malformations of lung	0.002	0.997	0.000
Q33.6 Hypoplasia and dysplasia of lung	0.002	0.997	0.000
Q33.5 Ectopic tissue in lung	0.002	0.997	0.000
Q33.4 Congenital bronchiectasis	0.002	0.997	0.000
Q33.3 Agenesis of lung	0.002	0.997	0.000
Q33.2 Sequestration of lung	0.002	0.997	0.000
Q33.1 Accessory lobe of lung	0.002	0.997	0.000
Q33.0 Congenital cystic lung	0.002	0.997	0.000
Q34.9 Congenital malformation of respiratory system, unspecified	0.002	0.997	0.000
Q34.8 Other specified congenital malformations of respiratory system	0.002	0.997	0.000
Q34.1 Congenital cyst of mediastinum	0.002	0.997	0.000
Q34.0 Anomaly of pleura	0.002	0.997	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.997	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.997	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.002	0.997	0.000
Q62.6 Malposition of ureter	0.002	0.997	0.000
Q62.4 Agenesis of ureter	0.002	0.997	0.000
Q62.0 Congenital hydronephrosis	0.002	0.997	0.000
Q90.9 Down's syndrome, unspecified	0.002	0.997	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.002	0.997	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.002	0.997	0.000
Q22.6 Hypoplastic right heart syndrome	0.002	0.997	0.000
Q22.4 Congenital tricuspid stenosis	0.002	0.997	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.002	0.997	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.002	0.997	0.000
Q22.0 Pulmonary valve atresia	0.002	0.997	0.000
Q90.2 Trisomy 21, translocation	0.002	0.997	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.002	0.997	0.000
H17.1 Other central corneal opacity	0.002	0.997	0.000
H17.0 Adherent leukoma	0.002	0.997	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.002	0.997	0.000
Q91.7 Patau's syndrome, unspecified	0.002	0.997	0.000
Q91.6 Trisomy 13, translocation	0.002	0.997	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.002	0.997	0.000
Q91.3 Edwards' syndrome, unspecified	0.002	0.997	0.000
Q91.2 Trisomy 18, translocation	0.002	0.997	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.002	0.997	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.002	0.997	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.002	0.997	0.000
Q92.7 Triploidy and polyploidy	0.002	0.997	0.000
Q92.6 Extra marker chromosomes	0.002	0.997	0.000
Q92.5 Duplications with other complex rearrangements	0.002	0.997	0.000
Q92.4 Duplications seen only at prometaphase	0.002	0.997	0.000
Q92.3 Minor partial trisomy	0.002	0.997	0.000
Q92.2 Major partial trisomy	0.002	0.997	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.002	0.997	0.000
Q93.9 Deletion from autosomes, unspecified	0.002	0.997	0.000
Q93.8 Other deletions from the autosomes	0.002	0.997	0.000
Q93.7 Deletions with other complex rearrangements	0.002	0.997	0.000
Q93.6 Deletions seen only at prometaphase	0.002	0.997	0.000
Q93.5 Other deletions of part of a chromosome	0.002	0.997	0.000
Q93.4 Deletion of short arm of chromosome 5	0.002	0.997	0.000
Q93.3 Deletion of short arm of chromosome 4	0.002	0.997	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.002	0.997	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.002	0.997	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.002	0.997	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.002	0.997	0.000
Q95.8 Other balanced rearrangements and structural markers	0.002	0.997	0.000
Q95.5 Individuals with autosomal fragile site	0.002	0.997	0.000
Q95.4 Individuals with marker heterochromatin	0.002	0.997	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.002	0.997	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.002	0.997	0.000
Q95.1 Chromosome inversion in normal individual	0.002	0.997	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.002	0.997	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.002	0.997	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.002	0.997	0.000
Q97.3 Female with 46,XY karyotype	0.002	0.997	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.002	0.997	0.000
Q97.1 Female with more than three X chromosomes	0.002	0.997	0.000
Q97.0 Karyotype 47,XXX	0.002	0.997	0.000
N64.0 Fissure and fistula of nipple	0.002	0.997	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.002	0.997	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.002	0.997	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.002	0.997	0.000
Q98.7 Male with sex chromosome mosaicism	0.002	0.997	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.002	0.997	0.000
Q98.5 Karyotype 47,XYY	0.002	0.997	0.000
Q98.3 Other male with 46,XX karyotype	0.002	0.997	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.002	0.997	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.002	0.997	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.002	0.997	0.000
Q24.6 Congenital heart block	0.002	0.998	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.002	0.998	0.000
R20.8 Other and unspecified disturbances of skin sensation	0.002	0.998	0.000
Q25 Congenital malformations of great arteries	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q61.8 Other cystic kidney diseases	0.002	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.002	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.002	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.002	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.002	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.002	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.002	0.998	0.000
Q96.0 Karyotype 45,X	0.002	0.998	0.000
M54.96 Dorsalgia, unspecified (Lumbar region)	0.000	0.998	0.002
N64.2 Atrophy of breast	0.002	0.998	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	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