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

rs398123916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123916(A;A)
Make rs398123916(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32468706
GeneDMD
is asnp
is mentioned by
dbSNPrs398123916
ebirs398123916
HLIrs398123916
Exacrs398123916
Varsomers398123916
Maprs398123916
PheGenIrs398123916
hapmaprs398123916
1000 genomesrs398123916
hgdprs398123916
ensemblrs398123916
gopubmedrs398123916
geneviewrs398123916
scholarrs398123916
googlers398123916
pharmgkbrs398123916
gwascentralrs398123916
openSNPrs398123916
23andMers398123916
23andMe allrs398123916
SNP Nexus

SNPshotrs398123916
SNPdbers398123916
MSV3drs398123916
GWAS Ctlgrs398123916
Max Magnitude0
ClinVar
Risk rs398123916(A;A)
Alt rs398123916(A;A)
Reference rs398123916(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32486823A>T
CLNSRC ClinVar Emory University
CLNACC RCV000080534.3,