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rs398123947

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123947(C;C)
Make rs398123947(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32438241
GeneDMD
is asnp
is mentioned by
dbSNPrs398123947
ebirs398123947
HLIrs398123947
Exacrs398123947
Varsomers398123947
Maprs398123947
PheGenIrs398123947
hapmaprs398123947
1000 genomesrs398123947
hgdprs398123947
ensemblrs398123947
gopubmedrs398123947
geneviewrs398123947
scholarrs398123947
googlers398123947
pharmgkbrs398123947
gwascentralrs398123947
openSNPrs398123947
23andMers398123947
23andMe allrs398123947
SNP Nexus

SNPshotrs398123947
SNPdbers398123947
MSV3drs398123947
GWAS Ctlgrs398123947
Max Magnitude0
ClinVar
Risk rs398123947(C;C)
Alt rs398123947(C;C)
Reference rs398123947(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32456358C>G
CLNSRC ClinVar Emory University
CLNACC RCV000080598.3,