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rs128626238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128626238(C;T)
Make rs128626238(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32699219
GeneDMD
is asnp
is mentioned by
dbSNPrs128626238
ebirs128626238
HLIrs128626238
Exacrs128626238
Varsomers128626238
Maprs128626238
PheGenIrs128626238
hapmaprs128626238
1000 genomesrs128626238
hgdprs128626238
ensemblrs128626238
gopubmedrs128626238
geneviewrs128626238
scholarrs128626238
googlers128626238
pharmgkbrs128626238
gwascentralrs128626238
openSNPrs128626238
23andMers128626238
23andMe allrs128626238
SNP Nexus

SNPshotrs128626238
SNPdbers128626238
MSV3drs128626238
GWAS Ctlgrs128626238
Max Magnitude0
OMIM300377
Desc
Variant0036
Relatedalso
ClinVar
Risk rs128626238(T;T)
Alt rs128626238(T;T)
Reference rs128626238(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32717336G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011993.11,