Have questions? Visit https://www.reddit.com/r/SNPedia

rs128626232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128626232(C;T)
Make rs128626232(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32545310
GeneDMD
is asnp
is mentioned by
dbSNPrs128626232
ebirs128626232
HLIrs128626232
Exacrs128626232
Varsomers128626232
Maprs128626232
PheGenIrs128626232
hapmaprs128626232
1000 genomesrs128626232
hgdprs128626232
ensemblrs128626232
gopubmedrs128626232
geneviewrs128626232
scholarrs128626232
googlers128626232
pharmgkbrs128626232
gwascentralrs128626232
openSNPrs128626232
23andMers128626232
23andMe allrs128626232
SNP Nexus

SNPshotrs128626232
SNPdbers128626232
MSV3drs128626232
GWAS Ctlgrs128626232
Max Magnitude0
OMIM300377
Desc
Variant0023
Relatedalso
ClinVar
Risk rs128626232(T;T)
Alt rs128626232(T;T)
Reference rs128626232(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32563427G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011984.17,