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rs398123891

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123891(G;G)
Make rs398123891(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491417
GeneDMD
is asnp
is mentioned by
dbSNPrs398123891
ebirs398123891
HLIrs398123891
Exacrs398123891
Varsomers398123891
Maprs398123891
PheGenIrs398123891
hapmaprs398123891
1000 genomesrs398123891
hgdprs398123891
ensemblrs398123891
gopubmedrs398123891
geneviewrs398123891
scholarrs398123891
googlers398123891
pharmgkbrs398123891
gwascentralrs398123891
openSNPrs398123891
23andMers398123891
23andMe allrs398123891
SNP Nexus

SNPshotrs398123891
SNPdbers398123891
MSV3drs398123891
GWAS Ctlgrs398123891
Max Magnitude0
ClinVar
Risk rs398123891(G;G)
Alt rs398123891(G;G)
Reference rs398123891(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32509534A>C
CLNSRC ClinVar Emory University
CLNACC RCV000080503.3,