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rs128626234

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128626234(C;T)
Make rs128626234(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32844794
GeneDMD
is asnp
is mentioned by
dbSNPrs128626234
ebirs128626234
HLIrs128626234
Exacrs128626234
Varsomers128626234
Maprs128626234
PheGenIrs128626234
hapmaprs128626234
1000 genomesrs128626234
hgdprs128626234
ensemblrs128626234
gopubmedrs128626234
geneviewrs128626234
scholarrs128626234
googlers128626234
pharmgkbrs128626234
gwascentralrs128626234
openSNPrs128626234
23andMers128626234
23andMe allrs128626234
SNP Nexus

SNPshotrs128626234
SNPdbers128626234
MSV3drs128626234
GWAS Ctlgrs128626234
Max Magnitude0
OMIM300377
Desc
Variant0031
Relatedalso
ClinVar
Risk rs128626234(T;T)
Alt rs128626234(T;T)
Reference rs128626234(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32862911G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011972.5,