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rs398123944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123944(-;-)
Make rs398123944(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32448545
GeneDMD
is asnp
is mentioned by
dbSNPrs398123944
ebirs398123944
HLIrs398123944
Exacrs398123944
Varsomers398123944
Maprs398123944
PheGenIrs398123944
hapmaprs398123944
1000 genomesrs398123944
hgdprs398123944
ensemblrs398123944
gopubmedrs398123944
geneviewrs398123944
scholarrs398123944
googlers398123944
pharmgkbrs398123944
gwascentralrs398123944
openSNPrs398123944
23andMers398123944
23andMe allrs398123944
SNP Nexus

SNPshotrs398123944
SNPdbers398123944
MSV3drs398123944
GWAS Ctlgrs398123944
Max Magnitude0
ClinVar
Risk rs398123944(;)
Alt rs398123944(;)
Reference rs398123944(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32466662delG
CLNSRC ClinVar
CLNACC RCV000080591.3,