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rs128627257

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs128627257(G;G)
Make rs128627257(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32310214
GeneDMD
is asnp
is mentioned by
dbSNPrs128627257
ClinGenrs128627257
ebirs128627257
HLIrs128627257
Exacrs128627257
Varsomers128627257
Maprs128627257
PheGenIrs128627257
hapmaprs128627257
1000 genomesrs128627257
hgdprs128627257
ensemblrs128627257
gopubmedrs128627257
geneviewrs128627257
scholarrs128627257
googlers128627257
pharmgkbrs128627257
gwascentralrs128627257
openSNPrs128627257
23andMers128627257
23andMe allrs128627257
SNP Nexus

SNPshotrs128627257
SNPdbers128627257
MSV3drs128627257
GWAS Ctlgrs128627257
Max Magnitude0
OMIM300377
Desc
Variant0084
Relatedalso
ClinVar
Risk rs128627257(G;G)
Alt rs128627257(G;G)
Reference Rs128627257(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32328331A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012042.17,