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rs128626251

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128626251(C;T)
Make rs128626251(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32216981
GeneDMD
is asnp
is mentioned by
dbSNPrs128626251
ebirs128626251
HLIrs128626251
Exacrs128626251
Varsomers128626251
Maprs128626251
PheGenIrs128626251
hapmaprs128626251
1000 genomesrs128626251
hgdprs128626251
ensemblrs128626251
gopubmedrs128626251
geneviewrs128626251
scholarrs128626251
googlers128626251
pharmgkbrs128626251
gwascentralrs128626251
openSNPrs128626251
23andMers128626251
23andMe allrs128626251
SNP Nexus

SNPshotrs128626251
SNPdbers128626251
MSV3drs128626251
GWAS Ctlgrs128626251
Max Magnitude0
OMIM300377
Desc
Variant0055
Relatedalso
ClinVar
Risk rs128626251(T;T)
Alt rs128626251(T;T)
Reference rs128626251(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy Dilated cardiomyopathy 3B Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Dilated cardiomyopathy 3B Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32235098G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000012012.7, RCV000150064.3, RCV000178554.1,