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rs61754457

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754457(A;A)
Make rs61754457(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032267
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754457
ebirs61754457
HLIrs61754457
Exacrs61754457
Varsomers61754457
Maprs61754457
PheGenIrs61754457
hapmaprs61754457
1000 genomesrs61754457
hgdprs61754457
ensemblrs61754457
gopubmedrs61754457
geneviewrs61754457
scholarrs61754457
googlers61754457
pharmgkbrs61754457
gwascentralrs61754457
openSNPrs61754457
23andMers61754457
23andMe allrs61754457
SNP Nexus

SNPshotrs61754457
SNPdbers61754457
MSV3drs61754457
GWAS Ctlgrs61754457
Max Magnitude0
ClinVar
Risk rs61754457(A,T;A,T)
Alt rs61754457(A,T;A,T)
Reference rs61754457(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297718C>A; NC_000023.10:g.153297718C>T
CLNSRC
CLNACC RCV000133068.2, RCV000133067.2,