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

rs398123953

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123953(C;T)
Make rs398123953(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32389644
GeneDMD
is asnp
is mentioned by
dbSNPrs398123953
ebirs398123953
HLIrs398123953
Exacrs398123953
Varsomers398123953
Maprs398123953
PheGenIrs398123953
hapmaprs398123953
1000 genomesrs398123953
hgdprs398123953
ensemblrs398123953
gopubmedrs398123953
geneviewrs398123953
scholarrs398123953
googlers398123953
pharmgkbrs398123953
gwascentralrs398123953
openSNPrs398123953
23andMers398123953
23andMe allrs398123953
SNP Nexus

SNPshotrs398123953
SNPdbers398123953
MSV3drs398123953
GWAS Ctlgrs398123953
Max Magnitude0
ClinVar
Risk rs398123953(T;T)
Alt rs398123953(T;T)
Reference rs398123953(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32407761G>A
CLNSRC HGMD
CLNACC RCV000080613.3, RCV000201013.1,