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rs61754421

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754421(C;C)
Make rs61754421(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032556
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754421
ebirs61754421
HLIrs61754421
Exacrs61754421
Varsomers61754421
Maprs61754421
PheGenIrs61754421
hapmaprs61754421
1000 genomesrs61754421
hgdprs61754421
ensemblrs61754421
gopubmedrs61754421
geneviewrs61754421
scholarrs61754421
googlers61754421
pharmgkbrs61754421
gwascentralrs61754421
openSNPrs61754421
23andMers61754421
23andMe allrs61754421
SNP Nexus

SNPshotrs61754421
SNPdbers61754421
MSV3drs61754421
GWAS Ctlgrs61754421
Max Magnitude0
ClinVar
Risk rs61754421(C,T;C,T)
Alt rs61754421(C,T;C,T)
Reference rs61754421(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153298007C>A; NC_000023.10:g.153298007C>G
CLNSRC
CLNACC RCV000133050.2, RCV000133049.2,