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rs398123913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123913(-;-)
Make rs398123913(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position33211285
GeneDMD
is asnp
is mentioned by
dbSNPrs398123913
ebirs398123913
HLIrs398123913
Exacrs398123913
Varsomers398123913
Maprs398123913
PheGenIrs398123913
hapmaprs398123913
1000 genomesrs398123913
hgdprs398123913
ensemblrs398123913
gopubmedrs398123913
geneviewrs398123913
scholarrs398123913
googlers398123913
pharmgkbrs398123913
gwascentralrs398123913
openSNPrs398123913
23andMers398123913
23andMe allrs398123913
SNP Nexus

SNPshotrs398123913
SNPdbers398123913
MSV3drs398123913
GWAS Ctlgrs398123913
Max Magnitude0
ClinVar
Risk rs398123913(;)
Alt rs398123913(;)
Reference rs398123913(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.33229402delA
CLNSRC ClinVar
CLNACC RCV000080531.4, RCV000173320.1, RCV000173321.1,