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rs398123941

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123941(G;T)
Make rs398123941(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32454763
GeneDMD
is asnp
is mentioned by
dbSNPrs398123941
ebirs398123941
HLIrs398123941
Exacrs398123941
Varsomers398123941
Maprs398123941
PheGenIrs398123941
hapmaprs398123941
1000 genomesrs398123941
hgdprs398123941
ensemblrs398123941
gopubmedrs398123941
geneviewrs398123941
scholarrs398123941
googlers398123941
pharmgkbrs398123941
gwascentralrs398123941
openSNPrs398123941
23andMers398123941
23andMe allrs398123941
SNP Nexus

SNPshotrs398123941
SNPdbers398123941
MSV3drs398123941
GWAS Ctlgrs398123941
Max Magnitude0
ClinVar
Risk rs398123941(T;T)
Alt rs398123941(T;T)
Reference rs398123941(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32472880C>A
CLNSRC ClinVar Emory University
CLNACC RCV000080584.3,