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rs398123874

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123874(-;-)
Make rs398123874(-;C)
Make rs398123874(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32844842
GeneDMD
is asnp
is mentioned by
dbSNPrs398123874
ebirs398123874
HLIrs398123874
Exacrs398123874
Varsomers398123874
Maprs398123874
PheGenIrs398123874
hapmaprs398123874
1000 genomesrs398123874
hgdprs398123874
ensemblrs398123874
gopubmedrs398123874
geneviewrs398123874
scholarrs398123874
googlers398123874
pharmgkbrs398123874
gwascentralrs398123874
openSNPrs398123874
23andMers398123874
23andMe allrs398123874
SNP Nexus

SNPshotrs398123874
SNPdbers398123874
MSV3drs398123874
GWAS Ctlgrs398123874
Max Magnitude0
ClinVar
Risk rs398123874(C;C)
Alt rs398123874(C;C)
Reference rs398123874(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32862960dupG
CLNSRC ClinVar
CLNACC RCV000080478.3,