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rs128626237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs128626237(A;A)
Make rs128626237(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32699252
GeneDMD
is asnp
is mentioned by
dbSNPrs128626237
ebirs128626237
HLIrs128626237
Exacrs128626237
Varsomers128626237
Maprs128626237
PheGenIrs128626237
hapmaprs128626237
1000 genomesrs128626237
hgdprs128626237
ensemblrs128626237
gopubmedrs128626237
geneviewrs128626237
scholarrs128626237
googlers128626237
pharmgkbrs128626237
gwascentralrs128626237
openSNPrs128626237
23andMers128626237
23andMe allrs128626237
SNP Nexus

SNPshotrs128626237
SNPdbers128626237
MSV3drs128626237
GWAS Ctlgrs128626237
Max Magnitude0
OMIM300377
Desc
Variant0035
Relatedalso
ClinVar
Risk rs128626237(A;A)
Alt rs128626237(A;A)
Reference rs128626237(T;T)
Significance Pathogenic
Disease Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32717369A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011992.17,