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rs61754441

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754441(-;-)
Make rs61754441(-;C)
Make rs61754441(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032368
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754441
ebirs61754441
HLIrs61754441
Exacrs61754441
Varsomers61754441
Maprs61754441
PheGenIrs61754441
hapmaprs61754441
1000 genomesrs61754441
hgdprs61754441
ensemblrs61754441
gopubmedrs61754441
geneviewrs61754441
scholarrs61754441
googlers61754441
pharmgkbrs61754441
gwascentralrs61754441
openSNPrs61754441
23andMers61754441
23andMe allrs61754441
SNP Nexus

SNPshotrs61754441
SNPdbers61754441
MSV3drs61754441
GWAS Ctlgrs61754441
Max Magnitude0
ClinVar
Risk rs61754441(CG,TG;CG,TG)
Alt rs61754441(CG,TG;CG,TG)
Reference rs61754441(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297819_153297820insA; NC_000023.10:g.153297820dupG
CLNSRC
CLNACC RCV000133033.2, RCV000133034.2,