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rs398123917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123917(C;T)
Make rs398123917(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32468683
GeneDMD
is asnp
is mentioned by
dbSNPrs398123917
ebirs398123917
HLIrs398123917
Exacrs398123917
Varsomers398123917
Maprs398123917
PheGenIrs398123917
hapmaprs398123917
1000 genomesrs398123917
hgdprs398123917
ensemblrs398123917
gopubmedrs398123917
geneviewrs398123917
scholarrs398123917
googlers398123917
pharmgkbrs398123917
gwascentralrs398123917
openSNPrs398123917
23andMers398123917
23andMe allrs398123917
SNP Nexus

SNPshotrs398123917
SNPdbers398123917
MSV3drs398123917
GWAS Ctlgrs398123917
Max Magnitude0
ClinVar
Risk rs398123917(T;T)
Alt rs398123917(T;T)
Reference rs398123917(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32486800G>A
CLNSRC HGMD
CLNACC RCV000080535.3,