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rs61748404

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61748404(C;G)
Make rs61748404(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031373
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748404
ebirs61748404
HLIrs61748404
Exacrs61748404
Varsomers61748404
Maprs61748404
PheGenIrs61748404
hapmaprs61748404
1000 genomesrs61748404
hgdprs61748404
ensemblrs61748404
gopubmedrs61748404
geneviewrs61748404
scholarrs61748404
googlers61748404
pharmgkbrs61748404
gwascentralrs61748404
openSNPrs61748404
23andMers61748404
23andMe allrs61748404
SNP Nexus

SNPshotrs61748404
SNPdbers61748404
MSV3drs61748404
GWAS Ctlgrs61748404
Max Magnitude0
ClinVar
Risk rs61748404(G;G)
Alt rs61748404(G;G)
Reference rs61748404(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296824G>C
CLNSRC
CLNACC RCV000133116.4,