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rs398123993

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123993(A;A)
Make rs398123993(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32343233
GeneDMD
is asnp
is mentioned by
dbSNPrs398123993
ebirs398123993
HLIrs398123993
Exacrs398123993
Varsomers398123993
Maprs398123993
PheGenIrs398123993
hapmaprs398123993
1000 genomesrs398123993
hgdprs398123993
ensemblrs398123993
gopubmedrs398123993
geneviewrs398123993
scholarrs398123993
googlers398123993
pharmgkbrs398123993
gwascentralrs398123993
openSNPrs398123993
23andMers398123993
23andMe allrs398123993
SNP Nexus

SNPshotrs398123993
SNPdbers398123993
MSV3drs398123993
GWAS Ctlgrs398123993
Max Magnitude0
ClinVar
Risk rs398123993(A;A)
Alt rs398123993(A;A)
Reference rs398123993(T;T)
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.32361350A>T
CLNSRC ClinVar Emory University
CLNACC RCV000080666.4, RCV000178431.1, RCV000178432.1,