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rs128626253

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128626253(G;T)
Make rs128626253(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31774100
GeneDMD
is asnp
is mentioned by
dbSNPrs128626253
ebirs128626253
HLIrs128626253
Exacrs128626253
Varsomers128626253
Maprs128626253
PheGenIrs128626253
hapmaprs128626253
1000 genomesrs128626253
hgdprs128626253
ensemblrs128626253
gopubmedrs128626253
geneviewrs128626253
scholarrs128626253
googlers128626253
pharmgkbrs128626253
gwascentralrs128626253
openSNPrs128626253
23andMers128626253
23andMe allrs128626253
SNP Nexus

SNPshotrs128626253
SNPdbers128626253
MSV3drs128626253
GWAS Ctlgrs128626253
Max Magnitude0
OMIM300377
Desc
Variant0060
Relatedalso
ClinVar
Risk rs128626253(T;T)
Alt rs128626253(T;T)
Reference rs128626253(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31792217C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012017.11,