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

rs398123893

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123893(-;-)
Make rs398123893(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32844796
GeneDMD
is asnp
is mentioned by
dbSNPrs398123893
ebirs398123893
HLIrs398123893
Exacrs398123893
Varsomers398123893
Maprs398123893
PheGenIrs398123893
hapmaprs398123893
1000 genomesrs398123893
hgdprs398123893
ensemblrs398123893
gopubmedrs398123893
geneviewrs398123893
scholarrs398123893
googlers398123893
pharmgkbrs398123893
gwascentralrs398123893
openSNPrs398123893
23andMers398123893
23andMe allrs398123893
SNP Nexus

SNPshotrs398123893
SNPdbers398123893
MSV3drs398123893
GWAS Ctlgrs398123893
Max Magnitude0
ClinVar
Risk rs398123893(;)
Alt rs398123893(;)
Reference rs398123893(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32862913delA
CLNSRC ClinVar
CLNACC RCV000080506.3,