Have questions? Visit https://www.reddit.com/r/SNPedia

rs797046135

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797046135(C;T)
Make rs797046135(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position28524525
GeneFOXN1
is asnp
is mentioned by
dbSNPrs797046135
ebirs797046135
HLIrs797046135
Exacrs797046135
Varsomers797046135
Maprs797046135
PheGenIrs797046135
hapmaprs797046135
1000 genomesrs797046135
hgdprs797046135
ensemblrs797046135
gopubmedrs797046135
geneviewrs797046135
scholarrs797046135
googlers797046135
pharmgkbrs797046135
gwascentralrs797046135
openSNPrs797046135
23andMers797046135
23andMe allrs797046135
SNP Nexus

SNPshotrs797046135
SNPdbers797046135
MSV3drs797046135
GWAS Ctlgrs797046135
Max Magnitude0
ClinVar
Risk rs797046135(T;T)
Alt rs797046135(T;T)
Reference rs797046135(C;C)
Significance Probable-Pathogenic
Disease Autistic disorder of childhood onset
Variation info
Gene FOXN1
CLNDBN Autistic disorder of childhood onset
Reversed 0
HGVS NC_000017.10:g.26851543C>T
CLNSRC Laboratorio de Genetica Humana\x3bUniversidad de los Andes
CLNACC RCV000192344.1,