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rs128625226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128625226(G;T)
Make rs128625226(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32454796
GeneDMD
is asnp
is mentioned by
dbSNPrs128625226
ebirs128625226
HLIrs128625226
Exacrs128625226
Varsomers128625226
Maprs128625226
PheGenIrs128625226
hapmaprs128625226
1000 genomesrs128625226
hgdprs128625226
ensemblrs128625226
gopubmedrs128625226
geneviewrs128625226
scholarrs128625226
googlers128625226
pharmgkbrs128625226
gwascentralrs128625226
openSNPrs128625226
23andMers128625226
23andMe allrs128625226
SNP Nexus

SNPshotrs128625226
SNPdbers128625226
MSV3drs128625226
GWAS Ctlgrs128625226
Max Magnitude0
OMIM300377
Desc
Variant0001
Relatedalso
ClinVar
Risk rs128625226(T;T)
Alt rs128625226(T;T)
Reference rs128625226(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32472913C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011958.11,