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rs398123973

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123973(C;T)
Make rs398123973(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32365049
GeneDMD
is asnp
is mentioned by
dbSNPrs398123973
ebirs398123973
HLIrs398123973
Exacrs398123973
Varsomers398123973
Maprs398123973
PheGenIrs398123973
hapmaprs398123973
1000 genomesrs398123973
hgdprs398123973
ensemblrs398123973
gopubmedrs398123973
geneviewrs398123973
scholarrs398123973
googlers398123973
pharmgkbrs398123973
gwascentralrs398123973
openSNPrs398123973
23andMers398123973
23andMe allrs398123973
SNP Nexus

SNPshotrs398123973
SNPdbers398123973
MSV3drs398123973
GWAS Ctlgrs398123973
Max Magnitude0
ClinVar
Risk rs398123973(T;T)
Alt rs398123973(T;T)
Reference rs398123973(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32383166G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080636.3,