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rs398123935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123935(C;T)
Make rs398123935(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32463576
GeneDMD
is asnp
is mentioned by
dbSNPrs398123935
ebirs398123935
HLIrs398123935
Exacrs398123935
Varsomers398123935
Maprs398123935
PheGenIrs398123935
hapmaprs398123935
1000 genomesrs398123935
hgdprs398123935
ensemblrs398123935
gopubmedrs398123935
geneviewrs398123935
scholarrs398123935
googlers398123935
pharmgkbrs398123935
gwascentralrs398123935
openSNPrs398123935
23andMers398123935
23andMe allrs398123935
SNP Nexus

SNPshotrs398123935
SNPdbers398123935
MSV3drs398123935
GWAS Ctlgrs398123935
Max Magnitude0
ClinVar
Risk rs398123935(T;T)
Alt rs398123935(T;T)
Reference rs398123935(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.32481693G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080573.4, RCV000176552.1, RCV000176553.1,