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rs398123872

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123872(C;T)
Make rs398123872(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32545295
GeneDMD
is asnp
is mentioned by
dbSNPrs398123872
ebirs398123872
HLIrs398123872
Exacrs398123872
Varsomers398123872
Maprs398123872
PheGenIrs398123872
hapmaprs398123872
1000 genomesrs398123872
hgdprs398123872
ensemblrs398123872
gopubmedrs398123872
geneviewrs398123872
scholarrs398123872
googlers398123872
pharmgkbrs398123872
gwascentralrs398123872
openSNPrs398123872
23andMers398123872
23andMe allrs398123872
SNP Nexus

SNPshotrs398123872
SNPdbers398123872
MSV3drs398123872
GWAS Ctlgrs398123872
Max Magnitude0
ClinVar
Risk rs398123872(G,T;G,T)
Alt rs398123872(G,T;G,T)
Reference rs398123872(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.32563412G>A
CLNSRC ClinVar Emory University
CLNACC RCV000080476.4, RCV000175181.1, RCV000175182.1,