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

rs398123998

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123998(A;A)
Make rs398123998(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32342215
GeneDMD
is asnp
is mentioned by
dbSNPrs398123998
ebirs398123998
HLIrs398123998
Exacrs398123998
Varsomers398123998
Maprs398123998
PheGenIrs398123998
hapmaprs398123998
1000 genomesrs398123998
hgdprs398123998
ensemblrs398123998
gopubmedrs398123998
geneviewrs398123998
scholarrs398123998
googlers398123998
pharmgkbrs398123998
gwascentralrs398123998
openSNPrs398123998
23andMers398123998
23andMe allrs398123998
SNP Nexus

SNPshotrs398123998
SNPdbers398123998
MSV3drs398123998
GWAS Ctlgrs398123998
Max Magnitude0
ClinVar
Risk rs398123998(A;A)
Alt rs398123998(A;A)
Reference rs398123998(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32360332A>T
CLNSRC ClinVar Emory University
CLNACC RCV000080672.3,