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rs398123828

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123828(A;A)
Make rs398123828(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31180369
GeneDMD
is asnp
is mentioned by
dbSNPrs398123828
ebirs398123828
HLIrs398123828
Exacrs398123828
Varsomers398123828
Maprs398123828
PheGenIrs398123828
hapmaprs398123828
1000 genomesrs398123828
hgdprs398123828
ensemblrs398123828
gopubmedrs398123828
geneviewrs398123828
scholarrs398123828
googlers398123828
pharmgkbrs398123828
gwascentralrs398123828
openSNPrs398123828
23andMers398123828
23andMe allrs398123828
SNP Nexus

SNPshotrs398123828
SNPdbers398123828
MSV3drs398123828
GWAS Ctlgrs398123828
Max Magnitude0
ClinVar
Risk rs398123828(A;A)
Alt rs398123828(A;A)
Reference rs398123828(G;G)
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.31198486C>T
CLNSRC HGMD
CLNACC RCV000080405.4, RCV000179688.1, RCV000179689.1,