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rs398123884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123884(C;C)
Make rs398123884(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32501754
GeneDMD
is asnp
is mentioned by
dbSNPrs398123884
ebirs398123884
HLIrs398123884
Exacrs398123884
Varsomers398123884
Maprs398123884
PheGenIrs398123884
hapmaprs398123884
1000 genomesrs398123884
hgdprs398123884
ensemblrs398123884
gopubmedrs398123884
geneviewrs398123884
scholarrs398123884
googlers398123884
pharmgkbrs398123884
gwascentralrs398123884
openSNPrs398123884
23andMers398123884
23andMe allrs398123884
SNP Nexus

SNPshotrs398123884
SNPdbers398123884
MSV3drs398123884
GWAS Ctlgrs398123884
Max Magnitude0
ClinVar
Risk rs398123884(C;C)
Alt rs398123884(C;C)
Reference rs398123884(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.32519871C>G
CLNSRC ClinVar
CLNACC RCV000080493.4, RCV000175444.1, RCV000175445.1,