Barely Significant
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Clinical Perspectives on Targeting Therapies for Personalized Medicine.

Adv Protein Chem Struct Biol · 2016 · PMC7102676 · PMID 26827603

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highly significantno p-value reported
The GWAS showed a single highly significant graded association of myopathy with the rs4363657 SNP within SLCO1B1 on chromosome 12 (odds ratio for myopathy: 4.5 (95% CI 2.6–7.7) per copy of the C allele; 16.9 (95% CI 4.7–61.1) in CC vs.

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