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rs398123964

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123964(G;T)
Make rs398123964(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32380620
GeneDMD
is asnp
is mentioned by
dbSNPrs398123964
ebirs398123964
HLIrs398123964
Exacrs398123964
Varsomers398123964
Maprs398123964
PheGenIrs398123964
hapmaprs398123964
1000 genomesrs398123964
hgdprs398123964
ensemblrs398123964
gopubmedrs398123964
geneviewrs398123964
scholarrs398123964
googlers398123964
pharmgkbrs398123964
gwascentralrs398123964
openSNPrs398123964
23andMers398123964
23andMe allrs398123964
SNP Nexus

SNPshotrs398123964
SNPdbers398123964
MSV3drs398123964
GWAS Ctlgrs398123964
Max Magnitude0
ClinVar
Risk rs398123964(T;T)
Alt rs398123964(T;T)
Reference rs398123964(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32398737C>A
CLNSRC ClinVar Emory University
CLNACC RCV000080626.3,