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rs128626239

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128626239(G;T)
Make rs128626239(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32699195
GeneDMD
is asnp
is mentioned by
dbSNPrs128626239
ebirs128626239
HLIrs128626239
Exacrs128626239
Varsomers128626239
Maprs128626239
PheGenIrs128626239
hapmaprs128626239
1000 genomesrs128626239
hgdprs128626239
ensemblrs128626239
gopubmedrs128626239
geneviewrs128626239
scholarrs128626239
googlers128626239
pharmgkbrs128626239
gwascentralrs128626239
openSNPrs128626239
23andMers128626239
23andMe allrs128626239
SNP Nexus

SNPshotrs128626239
SNPdbers128626239
MSV3drs128626239
GWAS Ctlgrs128626239
Max Magnitude0
OMIM300377
Desc
Variant0037
Relatedalso
ClinVar
Risk rs128626239(T;T)
Alt rs128626239(T;T)
Reference rs128626239(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32717312C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011994.17,