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rs128626231

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs128626231(G;G)
Make rs128626231(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32849753
GeneDMD
is asnp
is mentioned by
dbSNPrs128626231
ebirs128626231
HLIrs128626231
Exacrs128626231
Varsomers128626231
Maprs128626231
PheGenIrs128626231
hapmaprs128626231
1000 genomesrs128626231
hgdprs128626231
ensemblrs128626231
gopubmedrs128626231
geneviewrs128626231
scholarrs128626231
googlers128626231
pharmgkbrs128626231
gwascentralrs128626231
openSNPrs128626231
23andMers128626231
23andMe allrs128626231
SNP Nexus

SNPshotrs128626231
SNPdbers128626231
MSV3drs128626231
GWAS Ctlgrs128626231
Max Magnitude0
OMIM300377
Desc
Variant0020
Relatedalso
ClinVar
Risk rs128626231(G;G)
Alt rs128626231(G;G)
Reference rs128626231(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32867870A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011979.11,