Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123833(C;T)
Make rs398123833(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31178700
GeneDMD
is asnp
is mentioned by
dbSNPrs398123833
ebirs398123833
HLIrs398123833
Exacrs398123833
Varsomers398123833
Maprs398123833
PheGenIrs398123833
hapmaprs398123833
1000 genomesrs398123833
hgdprs398123833
ensemblrs398123833
gopubmedrs398123833
geneviewrs398123833
scholarrs398123833
googlers398123833
pharmgkbrs398123833
gwascentralrs398123833
openSNPrs398123833
23andMers398123833
23andMe allrs398123833
SNP Nexus

SNPshotrs398123833
SNPdbers398123833
MSV3drs398123833
GWAS Ctlgrs398123833
Max Magnitude0
ClinVar
Risk rs398123833(T;T)
Alt rs398123833(T;T)
Reference rs398123833(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31196817G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080414.3,