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rs62641234

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs62641234(A;T)
Make rs62641234(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032520
GeneMECP2
is asnp
is mentioned by
dbSNPrs62641234
ebirs62641234
HLIrs62641234
Exacrs62641234
Varsomers62641234
Maprs62641234
PheGenIrs62641234
hapmaprs62641234
1000 genomesrs62641234
hgdprs62641234
ensemblrs62641234
gopubmedrs62641234
geneviewrs62641234
scholarrs62641234
googlers62641234
pharmgkbrs62641234
gwascentralrs62641234
openSNPrs62641234
23andMers62641234
23andMe allrs62641234
SNP Nexus

SNPshotrs62641234
SNPdbers62641234
MSV3drs62641234
GWAS Ctlgrs62641234
Max Magnitude0
ClinVar
Risk rs62641234(T;T)
Alt rs62641234(T;T)
Reference rs62641234(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297971T>A
CLNSRC
CLNACC RCV000133187.2,