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rs128626236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128626236(A;A)
Make rs128626236(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32816495
GeneDMD
is asnp
is mentioned by
dbSNPrs128626236
ebirs128626236
HLIrs128626236
Exacrs128626236
Varsomers128626236
Maprs128626236
PheGenIrs128626236
hapmaprs128626236
1000 genomesrs128626236
hgdprs128626236
ensemblrs128626236
gopubmedrs128626236
geneviewrs128626236
scholarrs128626236
googlers128626236
pharmgkbrs128626236
gwascentralrs128626236
openSNPrs128626236
23andMers128626236
23andMe allrs128626236
SNP Nexus

SNPshotrs128626236
SNPdbers128626236
MSV3drs128626236
GWAS Ctlgrs128626236
Max Magnitude0
OMIM300377
Desc
Variant0033
Relatedalso
ClinVar
Risk rs128626236(A;A)
Alt rs128626236(A;A)
Reference rs128626236(C;C)
Significance Pathogenic
Disease Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32834612G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011981.17,