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rs398123887

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123887(G;T)
Make rs398123887(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491519
GeneDMD
is asnp
is mentioned by
dbSNPrs398123887
ebirs398123887
HLIrs398123887
Exacrs398123887
Varsomers398123887
Maprs398123887
PheGenIrs398123887
hapmaprs398123887
1000 genomesrs398123887
hgdprs398123887
ensemblrs398123887
gopubmedrs398123887
geneviewrs398123887
scholarrs398123887
googlers398123887
pharmgkbrs398123887
gwascentralrs398123887
openSNPrs398123887
23andMers398123887
23andMe allrs398123887
SNP Nexus

SNPshotrs398123887
SNPdbers398123887
MSV3drs398123887
GWAS Ctlgrs398123887
Max Magnitude0
ClinVar
Risk rs398123887(T;T)
Alt rs398123887(T;T)
Reference rs398123887(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.32509636C>A
CLNSRC ClinVar
CLNACC RCV000080496.4, RCV000176071.1, RCV000176072.1,