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rs128626240

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128626240(G;T)
Make rs128626240(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32614347
GeneDMD
is asnp
is mentioned by
dbSNPrs128626240
ebirs128626240
HLIrs128626240
Exacrs128626240
Varsomers128626240
Maprs128626240
PheGenIrs128626240
hapmaprs128626240
1000 genomesrs128626240
hgdprs128626240
ensemblrs128626240
gopubmedrs128626240
geneviewrs128626240
scholarrs128626240
googlers128626240
pharmgkbrs128626240
gwascentralrs128626240
openSNPrs128626240
23andMers128626240
23andMe allrs128626240
SNP Nexus

SNPshotrs128626240
SNPdbers128626240
MSV3drs128626240
GWAS Ctlgrs128626240
Max Magnitude0
OMIM300377
Desc
Variant0040
Relatedalso
ClinVar
Risk rs128626240(T;T)
Alt rs128626240(T;T)
Reference rs128626240(G;G)
Significance Pathogenic
Disease Intermediate muscular dystrophy
Variation info
Gene DMD
CLNDBN Intermediate muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32632464C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011998.17,