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rs61754455

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754455(A;A)
Make rs61754455(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032273
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754455
ebirs61754455
HLIrs61754455
Exacrs61754455
Varsomers61754455
Maprs61754455
PheGenIrs61754455
hapmaprs61754455
1000 genomesrs61754455
hgdprs61754455
ensemblrs61754455
gopubmedrs61754455
geneviewrs61754455
scholarrs61754455
googlers61754455
pharmgkbrs61754455
gwascentralrs61754455
openSNPrs61754455
23andMers61754455
23andMe allrs61754455
SNP Nexus

SNPshotrs61754455
SNPdbers61754455
MSV3drs61754455
GWAS Ctlgrs61754455
Max Magnitude0
ClinVar
Risk rs61754455(A;A)
Alt rs61754455(A;A)
Reference rs61754455(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297724C>T
CLNSRC
CLNACC RCV000133062.2,