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rs128625227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs128625227(G;T)
Make rs128625227(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32484931
GeneDMD
is asnp
is mentioned by
dbSNPrs128625227
ebirs128625227
HLIrs128625227
Exacrs128625227
Varsomers128625227
Maprs128625227
PheGenIrs128625227
hapmaprs128625227
1000 genomesrs128625227
hgdprs128625227
ensemblrs128625227
gopubmedrs128625227
geneviewrs128625227
scholarrs128625227
googlers128625227
pharmgkbrs128625227
gwascentralrs128625227
openSNPrs128625227
23andMers128625227
23andMe allrs128625227
SNP Nexus

SNPshotrs128625227
SNPdbers128625227
MSV3drs128625227
GWAS Ctlgrs128625227
Max Magnitude0
OMIM300377
Desc
Variant0003
Relatedalso
ClinVar
Risk rs128625227(T;T)
Alt rs128625227(T;T)
Reference rs128625227(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32503048C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011960.9,