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rs398123876

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123876(C;T)
Make rs398123876(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32545190
GeneDMD
is asnp
is mentioned by
dbSNPrs398123876
ebirs398123876
HLIrs398123876
Exacrs398123876
Varsomers398123876
Maprs398123876
PheGenIrs398123876
hapmaprs398123876
1000 genomesrs398123876
hgdprs398123876
ensemblrs398123876
gopubmedrs398123876
geneviewrs398123876
scholarrs398123876
googlers398123876
pharmgkbrs398123876
gwascentralrs398123876
openSNPrs398123876
23andMers398123876
23andMe allrs398123876
SNP Nexus

SNPshotrs398123876
SNPdbers398123876
MSV3drs398123876
GWAS Ctlgrs398123876
Max Magnitude0
ClinVar
Risk rs398123876(G,T;G,T)
Alt rs398123876(G,T;G,T)
Reference rs398123876(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32563307G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080480.3,