TreeWAS – Variant ID: rs11710456

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
Z09.8 Follow-up examination after other treatment for other conditions	0.000	0.970	0.030
E03.9 Hypothyroidism, unspecified	0.018	0.982	0.000
Z48.0 Attention to surgical dressings and sutures	0.012	0.988	0.000
E03 Other hypothyroidism	0.010	0.990	0.000
K07.3 Anomalies of tooth position	0.000	0.991	0.009
Z63.4 Disappearance and death of family member	0.000	0.991	0.009
W19.2 School, other institution and public administrative area	0.000	0.992	0.008
K07 Dentofacial anomalies [including malocclusion]	0.000	0.992	0.008
E03.1 Congenital hypothyroidism without goitre	0.008	0.992	0.000
K07.4 Malocclusion, unspecified	0.000	0.992	0.008
E03.0 Congenital hypothyroidism with diffuse goitre	0.007	0.992	0.000
E03.5 Myxoedema coma	0.007	0.993	0.000
E03.4 Atrophy of thyroid (acquired)	0.007	0.993	0.000
E03.3 Postinfectious hypothyroidism	0.007	0.993	0.000
E03.8 Other specified hypothyroidism	0.007	0.993	0.000
Q51 Congenital malformations of uterus and cervix	0.007	0.993	0.000
E03.2 Hypothyroidism due to medicaments and other exogenous substances	0.007	0.993	0.000
K07.2 Anomalies of dental arch relationship	0.000	0.993	0.007
K07.6 Temporomandibular joint disorders	0.000	0.993	0.007
Q50-Q56 Congenital malformations of genital organs	0.007	0.993	0.000
Z63 Other problems related to primary support group, including family circumstances	0.000	0.993	0.007
Z63.0 Problems in relationship with spouse or partner	0.000	0.993	0.007
Q51.4 Unicornate uterus	0.006	0.993	0.000
Z63.7 Other stressful life events affecting family and household	0.000	0.994	0.006
K07.1 Anomalies of jaw-cranial base relationship	0.000	0.994	0.006
Q51.3 Bicornate uterus	0.006	0.994	0.000
Q51.2 Other doubling of uterus	0.006	0.994	0.000
Q53 Undescended testicle	0.006	0.994	0.000
K07.8 Other dentofacial anomalies	0.000	0.994	0.006
K07.5 Dentofacial functional abnormalities	0.000	0.994	0.006
K07.0 Major anomalies of jaw size	0.000	0.994	0.006
Q52 Other congenital malformations of female genitalia	0.006	0.994	0.000
K07.9 Dentofacial anomaly, unspecified	0.000	0.994	0.006
Q51.8 Other congenital malformations of uterus and cervix	0.006	0.994	0.000
Q55 Other congenital malformations of male genital organs	0.005	0.994	0.000
H92.0 Otalgia	0.005	0.995	0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments	0.005	0.995	0.000
D22.7 Melanocytic naevi of lower limb, including hip	0.005	0.995	0.000
Q51.9 Congenital malformation of uterus and cervix, unspecified	0.005	0.995	0.000
Q51.7 Congenital fistulae between uterus and digestive and urinary tracts	0.005	0.995	0.000
Q51.6 Embryonic cyst of cervix	0.005	0.995	0.000
Q51.5 Agenesis and aplasia of cervix	0.005	0.995	0.000
Q51.1 Doubling of uterus with doubling of cervix and vagina	0.005	0.995	0.000
Q51.0 Agenesis and aplasia of uterus	0.005	0.995	0.000
L03.0 Cellulitis of finger and toe	0.005	0.995	0.000
Q52.4 Other congenital malformations of vagina	0.005	0.995	0.000
D23.3 Skin of other and unspecified parts of face	0.005	0.995	0.000
Z63.6 Dependent relative needing care at home	0.000	0.995	0.005
Q53.2 Undescended testicle, bilateral	0.005	0.995	0.000
Q54 Hypospadias	0.005	0.995	0.000
Q56 Indeterminate sex and pseudohermaphroditism	0.005	0.995	0.000
Z63.9 Problem related to primary support group, unspecified	0.000	0.995	0.005
Z63.3 Absence of family member	0.000	0.995	0.005
Z63.2 Inadequate family support	0.000	0.995	0.005
Z63.1 Problems in relationship with parents and in-laws	0.000	0.995	0.005
Q53.9 Undescended testicle, unspecified	0.005	0.995	0.000
Q52.5 Fusion of labia	0.005	0.995	0.000
Q50.4 Embryonic cyst of Fallopian tube	0.005	0.995	0.000
Q54.9 Hypospadias, unspecified	0.005	0.995	0.000
Q55.6 Other congenital malformations of penis	0.005	0.995	0.000
Q53.1 Undescended testicle, unilateral	0.005	0.995	0.000
Q53.0 Ectopic testis	0.004	0.995	0.000
Q52.9 Congenital malformation of female genitalia, unspecified	0.004	0.995	0.000
Q52.8 Other specified congenital malformations of female genitalia	0.004	0.995	0.000
Q52.7 Other congenital malformations of vulva	0.004	0.995	0.000
Q52.6 Congenital malformation of clitoris	0.004	0.995	0.000
Q52.3 Imperforate hymen	0.004	0.995	0.000
Q52.2 Congenital rectovaginal fistula	0.004	0.995	0.000
Q52.1 Doubling of vagina	0.004	0.995	0.000
Q52.0 Congenital absence of vagina	0.004	0.995	0.000
Z63.8 Other specified problems related to primary support group	0.000	0.995	0.004
H72.8 Other perforations of tympanic membrane	0.000	0.996	0.004
H72.9 Perforation of tympanic membrane, unspecified	0.000	0.996	0.004
Q54.1 Hypospadias, penile	0.004	0.996	0.000
Q55.9 Congenital malformation of male genital organ, unspecified	0.004	0.996	0.000
Q55.8 Other specified congenital malformations of male genital organs	0.004	0.996	0.000
Q55.5 Congenital absence and aplasia of penis	0.004	0.996	0.000
Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate	0.004	0.996	0.000
Q55.3 Atresia of vas deferens	0.004	0.996	0.000
Q55.2 Other congenital malformations of testis and scrotum	0.004	0.996	0.000
Q55.1 Hypoplasia of testis and scrotum	0.004	0.996	0.000
Q55.0 Absence and aplasia of testis	0.004	0.996	0.000
Q50.6 Other congenital malformatons of Fallopian tube and broad ligament	0.004	0.996	0.000
Q50.3 Other congenital malformations of ovary	0.004	0.996	0.000
Q50.2 Congenital torsion of ovary	0.004	0.996	0.000
Q50.1 Developmental ovarian cyst	0.004	0.996	0.000
Q50.0 Congenital absence of ovary	0.004	0.996	0.000
Q54.8 Other hypospadias	0.004	0.996	0.000
Q54.4 Congenital chordee	0.004	0.996	0.000
Q54.3 Hypospadias, perineal	0.004	0.996	0.000
Q54.2 Hypospadias, penoscrotal	0.004	0.996	0.000
N48.6 Balanitis xerotica obliterans	0.004	0.996	0.000
H72 Perforation of tympanic membrane	0.000	0.996	0.004
Q56.4 Indeterminate sex, unspecified	0.004	0.996	0.000
Q56.3 Pseudohermaphroditism, unspecified	0.004	0.996	0.000
Q56.2 Female pseudohermaphroditism, not elsewhere classified	0.004	0.996	0.000
Q56.1 Male pseudohermaphroditism, not elsewhere classified	0.004	0.996	0.000
Q56.0 Hermaphroditism, not elsewhere classified	0.004	0.996	0.000
S61.1 Open wound of finger(s) with damage to nail	0.004	0.996	0.000
S20.8 Superficial injuries of other and unspecified parts of thorax	0.000	0.996	0.004
H49.2 Sixth [abducent] nerve palsy	0.004	0.996	0.000
Q50.5 Embryonic cyst of broad ligament	0.004	0.996	0.000
Z63.5 Disruption of family by separation and divorce	0.000	0.996	0.004
N08.3 Glomerular disorders in diabetes mellitus	0.000	0.996	0.004
Q96.9 Turner's syndrome, unspecified	0.004	0.996	0.000
H92 Otalgia and effusion of ear	0.004	0.996	0.000
H92.1 Otorrhoea	0.004	0.996	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.004	0.996	0.000
H72.2 Other marginal perforations of tympanic membrane	0.000	0.996	0.004
Q96 Turner's syndrome	0.003	0.996	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.003	0.997	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.003	0.997	0.000
H02.6 Xanthelasma of eyelid	0.000	0.997	0.003
K51.8 Other ulcerative colitis	0.003	0.997	0.000
C34.9 Bronchus or lung, unspecified	0.000	0.997	0.003
H72.1 Attic perforation of tympanic membrane	0.000	0.997	0.003
S70.9 Superficial injury of hip and thigh, unspecified	0.000	0.997	0.003
G47.8 Other sleep disorders	0.003	0.997	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.003	0.997	0.000
N08.5 Glomerular disorders in systemic connective tissue disorders	0.000	0.997	0.003
S70.1 Contusion of thigh	0.000	0.997	0.003
R68.8 Other specified general symptoms and signs	0.000	0.997	0.003
H72.0 Central perforation of tympanic membrane	0.000	0.997	0.003
Q20-Q28 Congenital malformations of the circulatory system	0.003	0.997	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.003	0.997	0.000
H92.2 Otorrhagia	0.003	0.997	0.000
M50.2 Other cervical disk displacement	0.000	0.997	0.003
Q54.0 Hypospadias, balanic	0.003	0.997	0.000
L21.9 Seborrhoeic dermatitis, unspecified	0.003	0.997	0.000
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
Q96.8 Other variants of Turner's syndrome	0.003	0.997	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.003	0.997	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.003	0.997	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.003	0.997	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.003	0.997	0.000
Q96.0 Karyotype 45,X	0.003	0.997	0.000
V49.9 Car occupant [any] injured in unspecified traffic accident	0.003	0.997	0.000
N08 Glomerular disorders in diseases classified elsewhere	0.000	0.997	0.003
Q90 Down's syndrome	0.003	0.997	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.003	0.997	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.003	0.997	0.000
Q98.7 Male with sex chromosome mosaicism	0.003	0.997	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.003	0.997	0.000
Q98.5 Karyotype 47,XYY	0.003	0.997	0.000
Q98.3 Other male with 46,XX karyotype	0.003	0.997	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.003	0.997	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.003	0.997	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.003	0.997	0.000
M87.20 Osteonecrosis due to previous trauma (Multiple sites)	0.003	0.997	0.000
Q27.3 Peripheral arteriovenous malformation	0.003	0.997	0.000
Q40 Other congenital malformations of upper alimentary tract	0.003	0.997	0.000
I07.1 Tricuspid insufficiency	0.003	0.997	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.003	0.997	0.000
R41.3 Other amnesia	0.000	0.997	0.003
Q27 Other congenital malformations of peripheral vascular system	0.003	0.997	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.003	0.997	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.003	0.997	0.000
I22.9 Subsequent myocardial infarction of unspecified site	0.003	0.997	0.000
M06.34 Rheumatoid nodule (Hand)	0.003	0.997	0.000
C34 Malignant neoplasm of bronchus and lung	0.000	0.997	0.003
M65.91 Synovitis and tenosynovitis, unspecified (Shoulder region)	0.003	0.997	0.000
H50.1 Divergent concomitant strabismus	0.000	0.997	0.003
Q25 Congenital malformations of great arteries	0.003	0.997	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.997	0.000
W49.0 Home	0.003	0.997	0.000
M50.9 Cervical disk disorder, unspecified	0.000	0.997	0.002
Q35-Q37 Cleft lip and cleft palate	0.002	0.997	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.002	0.997	0.000
S92.20 Fracture of other tarsal bone(s) (closed)	0.000	0.997	0.002
Q44.6 Cystic disease of liver	0.002	0.997	0.000
M50 Cervical disk disorders	0.000	0.997	0.002
S70 Superficial injury of hip and thigh	0.000	0.997	0.002
S52.10 Fracture of upper end of radius (closed)	0.000	0.998	0.002
Q40.8 Other specified congenital malformations of upper alimentary tract	0.002	0.998	0.000
Q24 Other congenital malformations of heart	0.002	0.998	0.000
Q23 Congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.002	0.998	0.000
Q40.2 Other specified congenital malformations of stomach	0.002	0.998	0.000
D73.0 Hyposplenism	0.000	0.998	0.002
I31.9 Disease of pericardium, unspecified	0.000	0.998	0.002
Q22.1 Congenital pulmonary valve stenosis	0.002	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.002	0.998	0.000
Q25.3 Stenosis of aorta	0.002	0.998	0.000
Q26 Congenital malformations of great veins	0.002	0.998	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.002	0.998	0.000
M50.0 Cervical disk disorder with myelopathy	0.000	0.998	0.002
Q18.0 Sinus, fistula and cyst of branchial cleft	0.002	0.998	0.000
I35.2 Aortic (valve) stenosis with insufficiency	0.002	0.998	0.000
Q99.9 Chromosomal abnormality, unspecified	0.002	0.998	0.000
Q99.2 Fragile X chromosome	0.002	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.002	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.002	0.998	0.000
Q18 Other congenital malformations of face and neck	0.002	0.998	0.000
Q15 Other congenital malformations of eye	0.002	0.998	0.000
Q43 Other congenital malformations of intestine	0.002	0.998	0.000
L20.9 Atopic dermatitis, unspecified	0.002	0.998	0.000
M50.3 Other cervical disk degeneration	0.000	0.998	0.002
Q43.3 Congenital malformations of intestinal fixation	0.002	0.998	0.000
Q91.7 Patau's syndrome, unspecified	0.002	0.998	0.000
Q91.6 Trisomy 13, translocation	0.002	0.998	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.002	0.998	0.000
Q91.3 Edwards' syndrome, unspecified	0.002	0.998	0.000
Q91.2 Trisomy 18, translocation	0.002	0.998	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.002	0.998	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.002	0.998	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.002	0.998	0.000
Q92.7 Triploidy and polyploidy	0.002	0.998	0.000
Q92.6 Extra marker chromosomes	0.002	0.998	0.000
Q92.5 Duplications with other complex rearrangements	0.002	0.998	0.000
Q92.4 Duplications seen only at prometaphase	0.002	0.998	0.000
Q92.3 Minor partial trisomy	0.002	0.998	0.000
Q92.2 Major partial trisomy	0.002	0.998	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.002	0.998	0.000
Q93.9 Deletion from autosomes, unspecified	0.002	0.998	0.000
Q93.8 Other deletions from the autosomes	0.002	0.998	0.000
Q93.7 Deletions with other complex rearrangements	0.002	0.998	0.000
Q93.6 Deletions seen only at prometaphase	0.002	0.998	0.000
Q93.5 Other deletions of part of a chromosome	0.002	0.998	0.000
Q93.4 Deletion of short arm of chromosome 5	0.002	0.998	0.000
Q93.3 Deletion of short arm of chromosome 4	0.002	0.998	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.002	0.998	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.002	0.998	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.002	0.998	0.000
Q95.8 Other balanced rearrangements and structural markers	0.002	0.998	0.000
Q95.5 Individuals with autosomal fragile site	0.002	0.998	0.000
Q95.4 Individuals with marker heterochromatin	0.002	0.998	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.002	0.998	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.002	0.998	0.000
Q95.1 Chromosome inversion in normal individual	0.002	0.998	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.002	0.998	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.002	0.998	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.002	0.998	0.000
Q97.3 Female with 46,XY karyotype	0.002	0.998	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.002	0.998	0.000
Q97.1 Female with more than three X chromosomes	0.002	0.998	0.000
Q97.0 Karyotype 47,XXX	0.002	0.998	0.000
C34.3 Lower lobe, bronchus or lung	0.000	0.998	0.002
N08.8 Glomerular disorders in other diseases classified elsewhere	0.000	0.998	0.002
N08.4 Glomerular disorders in other endocrine, nutritional and metabolic diseases	0.000	0.998	0.002
N08.2 Glomerular disorders in blood diseases and disorders involving the immune mechanism	0.000	0.998	0.002
N08.1 Glomerular disorders in neoplastic diseases	0.000	0.998	0.002
N08.0 Glomerular disorders in infectious and parasitic diseases classified elsewhere	0.000	0.998	0.002
Q23.1 Congenital insufficiency of aortic valve	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
Q22.5 Ebstein's anomaly	0.002	0.998	0.000
Q90.2 Trisomy 21, translocation	0.002	0.998	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.002	0.998	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.002	0.998	0.000
C34.2 Middle lobe, bronchus or lung	0.000	0.998	0.002
M50.8 Other cervical disk disorders	0.000	0.998	0.002
Q12 Congenital lens malformations	0.002	0.998	0.000
C34.8 Overlapping lesion of bronchus and lung	0.000	0.998	0.002
M06.3 Rheumatoid nodule	0.002	0.998	0.000
Q90.9 Down's syndrome, unspecified	0.002	0.998	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.002	0.998	0.000
Q40.1 Congenital hiatus hernia	0.002	0.998	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.002	0.998	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.002	0.998	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.002	0.998	0.000
M06.37 Rheumatoid nodule (Ankle and foot)	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
Q16 Congenital malformations of ear causing impairment of hearing	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
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
Q22.4 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
Q22.0 Pulmonary valve atresia	0.002	0.998	0.000
Q25.6 Stenosis of pulmonary artery	0.002	0.998	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.002	0.998	0.000
M51.0 Lumbar and other intervertebral disk disorders with myelopathy	0.000	0.998	0.002
Q24.6 Congenital heart block	0.002	0.998	0.000
Q15.0 Congenital glaucoma	0.002	0.998	0.000
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
Q25.5 Atresia of pulmonary artery	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
L21 Seborrhoeic dermatitis	0.002	0.998	0.000
C34.1 Upper lobe, bronchus or lung	0.000	0.998	0.002
Q44.7 Other congenital malformations of liver	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q44.4 Choledochal cyst	0.002	0.998	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.002	0.998	0.000
Q44.2 Atresia of bile ducts	0.002	0.998	0.000
Q44.1 Other congenital malformations of gallbladder	0.002	0.998	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.002	0.998	0.000
M06.30 Rheumatoid nodule (Multiple sites)	0.002	0.998	0.000
D12.7 Rectosigmoid junction	0.000	0.998	0.002
G83.4 Cauda equina syndrome	0.000	0.998	0.002
M87.2 Osteonecrosis due to previous trauma	0.002	0.998	0.000
Q17 Other congenital malformations of ear	0.002	0.998	0.000
Q34 Other congenital malformations of respiratory system	0.002	0.998	0.000
Q33 Congenital malformations of lung	0.002	0.998	0.000
Q32 Congenital malformations of trachea and bronchus	0.002	0.998	0.000
Q31 Congenital malformations of larynx	0.002	0.998	0.000
Q30 Congenital malformations of nose	0.002	0.998	0.000
Q37 Cleft palate with cleft lip	0.002	0.998	0.000
Q36 Cleft lip	0.002	0.998	0.000
Q35 Cleft palate	0.002	0.998	0.000
C34.0 Main bronchus	0.000	0.998	0.002
L27.0 Generalised skin eruption due to drugs and medicaments	0.002	0.998	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.002	0.998	0.000
S70.7 Multiple superficial injuries of hip and thigh	0.000	0.998	0.002
Q21 Congenital malformations of cardiac septa	0.002	0.998	0.000
Q24.0 Dextrocardia	0.002	0.998	0.000
Q25.1 Coarctation of aorta	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
M80.50 Idiopathic osteoporosis with pathological fracture (Multiple sites)	0.002	0.998	0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.002	0.998	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.002	0.998	0.000
Q23.4 Hypoplastic left heart syndrome	0.002	0.998	0.000
Q23.2 Congenital mitral stenosis	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
Q25.4 Other congenital malformations of aorta	0.002	0.998	0.000
Q45 Other congenital malformations of digestive system	0.002	0.998	0.000
I49.0 Ventricular fibrillation and flutter	0.002	0.998	0.000
Q23.3 Congenital mitral insufficiency	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
S72.30 Fracture of shaft of femur (closed)	0.000	0.998	0.002
A69.2 Lyme disease	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
Q24.8 Other specified congenital malformations of heart	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
L20 Atopic dermatitis	0.002	0.998	0.000
Q15.9 Congenital malformation of eye, unspecified	0.002	0.998	0.000
Q15.8 Other specified congenital malformations of eye	0.002	0.998	0.000
Q18.9 Congenital malformation of face and neck, unspecified	0.002	0.998	0.000
Q18.8 Other specified congenital malformations of face and neck	0.002	0.998	0.000
Q18.7 Microcheilia	0.002	0.998	0.000
Q18.6 Macrocheilia	0.002	0.998	0.000
Q18.5 Microstomia	0.002	0.998	0.000
Q18.4 Macrostomia	0.002	0.998	0.000
Q18.3 Webbing of neck	0.002	0.998	0.000
Q18.2 Other branchial cleft malformations	0.002	0.998	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.002	0.998	0.000
Q43.7 Persistent cloaca	0.002	0.998	0.000
Q43.6 Congenital fistula of rectum and anus	0.002	0.998	0.000
Q43.5 Ectopic anus	0.002	0.998	0.000
Q43.4 Duplication of intestine	0.002	0.998	0.000
Q43.2 Other congenital functional disorders of colon	0.002	0.998	0.000
T22.0 Burn of unspecified degree of shoulder and upper limb, except wrist and hand	0.002	0.998	0.000
Q28 Other congenital malformations of circulatory system	0.002	0.998	0.000
V49 Car occupant injured in other and unspecified transport accidents	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
M24.41 Recurrent dislocation and subluxation of joint (Shoulder region)	0.002	0.998	0.000
Q12.0 Congenital cataract	0.002	0.998	0.000
Q21.3 Tetralogy of Fallot	0.002	0.998	0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.002	0.998	0.000
Q04 Other congenital malformations of brain	0.002	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.002	0.998	0.000
Q03 Congenital hydrocephalus	0.002	0.998	0.000
Q01 Encephalocele	0.002	0.998	0.000
Q00 Anencephaly and similar malformations	0.002	0.998	0.000
Q02 Microcephaly	0.002	0.998	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
M87.24 Osteonecrosis due to previous trauma (Hand)	0.002	0.998	0.000
L27 Dermatitis due to substances taken internally	0.002	0.998	0.000
T22 Burn and corrosion of shoulder and upper limb, except wrist and hand	0.002	0.998	0.000
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
Q43.8 Other specified congenital malformations of intestine	0.002	0.998	0.000
M06.39 Rheumatoid nodule (Site unspecified)	0.002	0.998	0.000
M06.38 Rheumatoid nodule (Other)	0.002	0.998	0.000
M06.36 Rheumatoid nodule (Lower leg)	0.002	0.998	0.000
M06.35 Rheumatoid nodule (Pelvic region and thigh)	0.002	0.998	0.000
M06.33 Rheumatoid nodule (Forearm)	0.002	0.998	0.000
M06.31 Rheumatoid nodule (Shoulder region)	0.002	0.998	0.000
G12.2 Motor neuron disease	0.000	0.998	0.002
L27.2 Dermatitis due to ingested food	0.002	0.998	0.000
T24.0 Burn of unspecified degree of hip and lower limb, except ankle and foot	0.002	0.998	0.000
Q24.5 Malformation of coronary vessels	0.002	0.998	0.000
Q43.1 Hirschsprung's disease	0.002	0.998	0.000
V49.5 Passenger injured in collision with other and unspecified motor vehicles in traffic accident	0.002	0.998	0.000
M06.32 Rheumatoid nodule (Upper arm)	0.002	0.998	0.000
M87.27 Osteonecrosis due to previous trauma (Ankle and foot)	0.002	0.998	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.002	0.998	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.002	0.998	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.002	0.998	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.002	0.998	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.002	0.998	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.002	0.998	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.002	0.998	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.002	0.998	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.002	0.998	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.002	0.998	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.002	0.998	0.000
L20.8 Other atopic dermatitis	0.002	0.998	0.000
Q07.8 Other specified congenital malformations of nervous system	0.002	0.998	0.000
Q11.3 Macrophthalmos	0.002	0.998	0.000
Q11.2 Microphthalmos	0.002	0.998	0.000
Q11.0 Cystic eyeball	0.002	0.998	0.000
Q13.9 Congenital malformation of anterior segment of eye, unspecified	0.002	0.998	0.000
Q13.8 Other congenital malformations of anterior segment of eye	0.002	0.998	0.000
Q13.5 Blue sclera	0.002	0.998	0.000
Q13.4 Other congenital corneal malformations	0.002	0.998	0.000
Q13.3 Congenital corneal opacity	0.002	0.998	0.000
Q13.2 Other congenital malformations of iris	0.002	0.998	0.000
Q13.1 Absence of iris	0.002	0.998	0.000
Q13.0 Coloboma of iris	0.002	0.998	0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.002	0.998	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.002	0.998	0.000
Q14.3 Congenital malformation of choroid	0.002	0.998	0.000
Q14.2 Congenital malformation of optic disk	0.002	0.998	0.000
Q14.1 Congenital malformation of retina	0.002	0.998	0.000
Q14.0 Congenital malformation of vitreous humour	0.002	0.998	0.000
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified	0.002	0.998	0.000
Q16.5 Congenital malformation of inner ear	0.002	0.998	0.000
Q16.4 Other congenital malformations of middle ear	0.002	0.998	0.000
Q16.3 Congenital malformation of ear ossicles	0.002	0.998	0.000
Q16.2 Absence of eustachian tube	0.002	0.998	0.000
Q16.1 Congenital absence, atresia and stricture of auditory canal (external)	0.002	0.998	0.000
Q16.0 Congenital absence of (ear) auricle	0.002	0.998	0.000
T22.3 Burn of third degree of shoulder and upper limb, except wrist and hand	0.002	0.998	0.000
Q11.1 Other anophthalmos	0.002	0.998	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.002	0.998	0.000
T22.1 Burn of first degree of shoulder and upper limb, except wrist and hand	0.002	0.998	0.000
T81.3 Disruption of operation wound, not elsewhere classified	0.002	0.998	0.000
R68 Other general symptoms and signs	0.000	0.998	0.002
E24.9 Cushing's syndrome, unspecified	0.000	0.998	0.002
K22.4 Dyskinesia of oesophagus	0.000	0.998	0.002
L21.8 Other seborrhoeic dermatitis	0.002	0.998	0.000
L21.1 Seborrhoeic infantile dermatitis	0.002	0.998	0.000
L21.0 Seborrhoea capitis	0.002	0.998	0.000
L89.9 Decubitus ulcer and pressure area, unspecified	0.000	0.998	0.002
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.002	0.998	0.000
Q87.4 Marfan's syndrome	0.002	0.998	0.000
T92.1 Sequelae of fracture of arm	0.000	0.998	0.002
S70.0 Contusion of hip	0.000	0.998	0.002
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
M47.87 Other spondylosis (Lumbosacral region)	0.002	0.998	0.000
M87.29 Osteonecrosis due to previous trauma (Site unspecified)	0.002	0.998	0.000
M87.28 Osteonecrosis due to previous trauma (Other)	0.002	0.998	0.000
M87.26 Osteonecrosis due to previous trauma (Lower leg)	0.002	0.998	0.000
M87.25 Osteonecrosis due to previous trauma (Pelvic region and thigh)	0.002	0.998	0.000
M87.23 Osteonecrosis due to previous trauma (Forearm)	0.002	0.998	0.000
M87.22 Osteonecrosis due to previous trauma (Upper arm)	0.002	0.998	0.000
M87.21 Osteonecrosis due to previous trauma (Shoulder region)	0.002	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
Q30.9 Congenital malformation of nose, unspecified	0.001	0.998	0.000
Q30.8 Other congenital malformations of nose	0.001	0.998	0.000
Q30.3 Congenital perforated nasal septum	0.001	0.998	0.000
Q30.2 Fissured, notched and cleft nose	0.001	0.998	0.000
Q30.1 Agenesis and underdevelopment of nose	0.001	0.998	0.000
Q30.0 Choanal atresia	0.001	0.998	0.000
Q31.9 Congenital malformation of larynx, unspecified	0.001	0.998	0.000
Q31.8 Other congenital malformations of larynx	0.001	0.998	0.000
Q31.5 Congenital laryngomalacia	0.001	0.998	0.000
Q31.4 Congenital laryngeal stridor	0.001	0.998	0.000
Q31.3 Laryngocele	0.001	0.998	0.000
Q31.2 Laryngeal hypoplasia	0.001	0.998	0.000
Q31.1 Congenital subglottic stenosis	0.001	0.998	0.000
Q31.0 Web of larynx	0.001	0.998	0.000
Q32.4 Other congenital malformations of bronchus	0.001	0.998	0.000
Q32.3 Congenital stenosis of bronchus	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