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rs878853113

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853113(C;C)
Make rs878853113(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position15239545
GenePMP22
is asnp
is mentioned by
dbSNPrs878853113
ebirs878853113
HLIrs878853113
Exacrs878853113
Varsomers878853113
Maprs878853113
PheGenIrs878853113
hapmaprs878853113
1000 genomesrs878853113
hgdprs878853113
ensemblrs878853113
gopubmedrs878853113
geneviewrs878853113
scholarrs878853113
googlers878853113
pharmgkbrs878853113
gwascentralrs878853113
openSNPrs878853113
23andMers878853113
23andMe allrs878853113
SNP Nexus

SNPshotrs878853113
SNPdbers878853113
MSV3drs878853113
GWAS Ctlgrs878853113
Max Magnitude0
ClinVar
Risk rs878853113(C;C)
Alt rs878853113(C;C)
Reference rs878853113(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PMP22
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.15142862A>G
CLNSRC
CLNACC RCV000224582.1,