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rs398123934

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123934(A;A)
Make rs398123934(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32464585
GeneDMD
is asnp
is mentioned by
dbSNPrs398123934
ebirs398123934
HLIrs398123934
Exacrs398123934
Varsomers398123934
Maprs398123934
PheGenIrs398123934
hapmaprs398123934
1000 genomesrs398123934
hgdprs398123934
ensemblrs398123934
gopubmedrs398123934
geneviewrs398123934
scholarrs398123934
googlers398123934
pharmgkbrs398123934
gwascentralrs398123934
openSNPrs398123934
23andMers398123934
23andMe allrs398123934
SNP Nexus

SNPshotrs398123934
SNPdbers398123934
MSV3drs398123934
GWAS Ctlgrs398123934
Max Magnitude0
ClinVar
Risk rs398123934(A;A)
Alt rs398123934(A;A)
Reference rs398123934(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.32482702C>T
CLNSRC ClinVar
CLNACC RCV000080572.4, RCV000176478.1, RCV000176479.1,