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rs61754425

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61754425(C;T)
Make rs61754425(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032529
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754425
ebirs61754425
HLIrs61754425
Exacrs61754425
Varsomers61754425
Maprs61754425
PheGenIrs61754425
hapmaprs61754425
1000 genomesrs61754425
hgdprs61754425
ensemblrs61754425
gopubmedrs61754425
geneviewrs61754425
scholarrs61754425
googlers61754425
pharmgkbrs61754425
gwascentralrs61754425
openSNPrs61754425
23andMers61754425
23andMe allrs61754425
SNP Nexus

SNPshotrs61754425
SNPdbers61754425
MSV3drs61754425
GWAS Ctlgrs61754425
Max Magnitude0
ClinVar
Risk rs61754425(T;T)
Alt rs61754425(T;T)
Reference rs61754425(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297980G>A
CLNSRC
CLNACC RCV000133160.2,