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rs61754437

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61754437(C;G)
Make rs61754437(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032390
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754437
ebirs61754437
HLIrs61754437
Exacrs61754437
Varsomers61754437
Maprs61754437
PheGenIrs61754437
hapmaprs61754437
1000 genomesrs61754437
hgdprs61754437
ensemblrs61754437
gopubmedrs61754437
geneviewrs61754437
scholarrs61754437
googlers61754437
pharmgkbrs61754437
gwascentralrs61754437
openSNPrs61754437
23andMers61754437
23andMe allrs61754437
SNP Nexus

SNPshotrs61754437
SNPdbers61754437
MSV3drs61754437
GWAS Ctlgrs61754437
Max Magnitude0
ClinVar
Risk rs61754437(G;G)
Alt rs61754437(G;G)
Reference rs61754437(C;C)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297841G>C
CLNSRC
CLNACC RCV000133029.2, RCV000193745.1,