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rs878853312

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853312(C;T)
Make rs878853312(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154031178
GeneMECP2
is asnp
is mentioned by
dbSNPrs878853312
ebirs878853312
HLIrs878853312
Exacrs878853312
Varsomers878853312
Maprs878853312
PheGenIrs878853312
hapmaprs878853312
1000 genomesrs878853312
hgdprs878853312
ensemblrs878853312
gopubmedrs878853312
geneviewrs878853312
scholarrs878853312
googlers878853312
pharmgkbrs878853312
gwascentralrs878853312
openSNPrs878853312
23andMers878853312
23andMe allrs878853312
SNP Nexus

SNPshotrs878853312
SNPdbers878853312
MSV3drs878853312
GWAS Ctlgrs878853312
Max Magnitude0
ClinVar
Risk rs878853312(T;T)
Alt rs878853312(T;T)
Reference rs878853312(C;C)
Significance Probable-Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296629G>A
CLNSRC
CLNACC RCV000225456.1,