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rs1800278(G;G)

From SNPedia

Is agenotype
ofrs1800278
GeneDMD
ChromosomeX
Position31,478,309
mentionedby
Magnitude0.5
Geno Mag Summary
(A;A) 0 common in clinvar
(G;G) 0.5

omim notes that [PMID 7881286] links this snp to DUCHENNE MUSCULAR DYSTROPHY, but hapmap frequency makes that seem very unlikely.