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

rs61751444

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61751444(C;T)
Make rs61751444(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154030903
GeneMECP2
is asnp
is mentioned by
dbSNPrs61751444
ebirs61751444
HLIrs61751444
Exacrs61751444
Varsomers61751444
Maprs61751444
PheGenIrs61751444
hapmaprs61751444
1000 genomesrs61751444
hgdprs61751444
ensemblrs61751444
gopubmedrs61751444
geneviewrs61751444
scholarrs61751444
googlers61751444
pharmgkbrs61751444
gwascentralrs61751444
openSNPrs61751444
23andMers61751444
23andMe allrs61751444
SNP Nexus

SNPshotrs61751444
SNPdbers61751444
MSV3drs61751444
GWAS Ctlgrs61751444
Max Magnitude0


ClinVar
Risk rs61751444(T;T)
Alt rs61751444(T;T)
Reference rs61751444(C;C)
Significance Pathogenic
Disease not provided Mental retardation Autism Rett syndrome not specified
Variation info
Gene MECP2
CLNDBN not provided Mental retardation, X-linked, syndromic 13 Autism, susceptibility to, X-linked 3 Rett syndrome not specified
Reversed 1
HGVS NC_000023.10:g.153296354G>A
CLNSRC ClinVar GeneDx
CLNACC RCV000133293.5, RCV000169947.1, RCV000170240.1, RCV000170241.1, RCV000193139.1,