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rs128625228

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128625228(C;T)
Make rs128625228(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32345978
GeneDMD
is asnp
is mentioned by
dbSNPrs128625228
ebirs128625228
HLIrs128625228
Exacrs128625228
Varsomers128625228
Maprs128625228
PheGenIrs128625228
hapmaprs128625228
1000 genomesrs128625228
hgdprs128625228
ensemblrs128625228
gopubmedrs128625228
geneviewrs128625228
scholarrs128625228
googlers128625228
pharmgkbrs128625228
gwascentralrs128625228
openSNPrs128625228
23andMers128625228
23andMe allrs128625228
SNP Nexus

SNPshotrs128625228
SNPdbers128625228
MSV3drs128625228
GWAS Ctlgrs128625228
Max Magnitude0
OMIM300377
Desc
Variant0004
Relatedalso
ClinVar
Risk rs128625228(T;T)
Alt rs128625228(T;T)
Reference rs128625228(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32364095G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011961.12,