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

rs61754426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61754426(-;-)
Make rs61754426(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032508
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754426
ebirs61754426
HLIrs61754426
Exacrs61754426
Varsomers61754426
Maprs61754426
PheGenIrs61754426
hapmaprs61754426
1000 genomesrs61754426
hgdprs61754426
ensemblrs61754426
gopubmedrs61754426
geneviewrs61754426
scholarrs61754426
googlers61754426
pharmgkbrs61754426
gwascentralrs61754426
openSNPrs61754426
23andMers61754426
23andMe allrs61754426
SNP Nexus

SNPshotrs61754426
SNPdbers61754426
MSV3drs61754426
GWAS Ctlgrs61754426
Max Magnitude0
ClinVar
Risk rs61754426(;)
Alt rs61754426(;)
Reference rs61754426(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297959delG
CLNSRC
CLNACC RCV000133236.2,