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rs128626233

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128626233(C;T)
Make rs128626233(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32849736
GeneDMD
is asnp
is mentioned by
dbSNPrs128626233
ebirs128626233
HLIrs128626233
Exacrs128626233
Varsomers128626233
Maprs128626233
PheGenIrs128626233
hapmaprs128626233
1000 genomesrs128626233
hgdprs128626233
ensemblrs128626233
gopubmedrs128626233
geneviewrs128626233
scholarrs128626233
googlers128626233
pharmgkbrs128626233
gwascentralrs128626233
openSNPrs128626233
23andMers128626233
23andMe allrs128626233
SNP Nexus

SNPshotrs128626233
SNPdbers128626233
MSV3drs128626233
GWAS Ctlgrs128626233
Max Magnitude0
OMIM300377
Desc
Variant0029
Relatedalso
ClinVar
Risk rs128626233(T;T)
Alt rs128626233(T;T)
Reference rs128626233(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32867853G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011990.11,