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rs398123939

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123939(A;A)
Make rs398123939(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32454833
GeneDMD
is asnp
is mentioned by
dbSNPrs398123939
ebirs398123939
HLIrs398123939
Exacrs398123939
Varsomers398123939
Maprs398123939
PheGenIrs398123939
hapmaprs398123939
1000 genomesrs398123939
hgdprs398123939
ensemblrs398123939
gopubmedrs398123939
geneviewrs398123939
scholarrs398123939
googlers398123939
pharmgkbrs398123939
gwascentralrs398123939
openSNPrs398123939
23andMers398123939
23andMe allrs398123939
SNP Nexus

SNPshotrs398123939
SNPdbers398123939
MSV3drs398123939
GWAS Ctlgrs398123939
Max Magnitude0
ClinVar
Risk rs398123939(A;A)
Alt rs398123939(A;A)
Reference rs398123939(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32472950C>T
CLNSRC ClinVar
CLNACC RCV000080582.3,