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rs398123970

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123970(A;A)
Make rs398123970(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32816509
GeneDMD
is asnp
is mentioned by
dbSNPrs398123970
ebirs398123970
HLIrs398123970
Exacrs398123970
Varsomers398123970
Maprs398123970
PheGenIrs398123970
hapmaprs398123970
1000 genomesrs398123970
hgdprs398123970
ensemblrs398123970
gopubmedrs398123970
geneviewrs398123970
scholarrs398123970
googlers398123970
pharmgkbrs398123970
gwascentralrs398123970
openSNPrs398123970
23andMers398123970
23andMe allrs398123970
SNP Nexus

SNPshotrs398123970
SNPdbers398123970
MSV3drs398123970
GWAS Ctlgrs398123970
Max Magnitude0
ClinVar
Risk rs398123970(A;A)
Alt rs398123970(A;A)
Reference rs398123970(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32834626C>T
CLNSRC ClinVar Emory University
CLNACC RCV000080633.3,