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rs398123981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123981(C;T)
Make rs398123981(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32362826
GeneDMD
is asnp
is mentioned by
dbSNPrs398123981
ebirs398123981
HLIrs398123981
Exacrs398123981
Varsomers398123981
Maprs398123981
PheGenIrs398123981
hapmaprs398123981
1000 genomesrs398123981
hgdprs398123981
ensemblrs398123981
gopubmedrs398123981
geneviewrs398123981
scholarrs398123981
googlers398123981
pharmgkbrs398123981
gwascentralrs398123981
openSNPrs398123981
23andMers398123981
23andMe allrs398123981
SNP Nexus

SNPshotrs398123981
SNPdbers398123981
MSV3drs398123981
GWAS Ctlgrs398123981
Max Magnitude0
ClinVar
Risk rs398123981(T;T)
Alt rs398123981(T;T)
Reference rs398123981(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32380943G>A
CLNSRC HGMD
CLNACC RCV000080648.4, RCV000177911.1, RCV000177912.2,