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rs398123910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123910(A;A)
Make rs398123910(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32472297
GeneDMD
is asnp
is mentioned by
dbSNPrs398123910
ebirs398123910
HLIrs398123910
Exacrs398123910
Varsomers398123910
Maprs398123910
PheGenIrs398123910
hapmaprs398123910
1000 genomesrs398123910
hgdprs398123910
ensemblrs398123910
gopubmedrs398123910
geneviewrs398123910
scholarrs398123910
googlers398123910
pharmgkbrs398123910
gwascentralrs398123910
openSNPrs398123910
23andMers398123910
23andMe allrs398123910
SNP Nexus

SNPshotrs398123910
SNPdbers398123910
MSV3drs398123910
GWAS Ctlgrs398123910
Max Magnitude0
ClinVar
Risk rs398123910(A;A)
Alt rs398123910(A;A)
Reference rs398123910(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.32490414A>T
CLNSRC ClinVar Emory University
CLNACC RCV000080526.4, RCV000176299.1, RCV000176300.1,