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rs398123831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123831(-;-)
Make rs398123831(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31178725
GeneDMD
is asnp
is mentioned by
dbSNPrs398123831
ebirs398123831
HLIrs398123831
Exacrs398123831
Varsomers398123831
Maprs398123831
PheGenIrs398123831
hapmaprs398123831
1000 genomesrs398123831
hgdprs398123831
ensemblrs398123831
gopubmedrs398123831
geneviewrs398123831
scholarrs398123831
googlers398123831
pharmgkbrs398123831
gwascentralrs398123831
openSNPrs398123831
23andMers398123831
23andMe allrs398123831
SNP Nexus

SNPshotrs398123831
SNPdbers398123831
MSV3drs398123831
GWAS Ctlgrs398123831
Max Magnitude0
ClinVar
Risk rs398123831(;)
Alt rs398123831(;)
Reference rs398123831(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31196842delA
CLNSRC ClinVar
CLNACC RCV000080412.3,