Barely Significant
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SLCO1B1 Polymorphisms and Statin-Induced Myopathy.

PLoS Curr · 2013 · PMC3871416 · PMID 24459608

Europe PMCDOI
1
hedged sentence
0.0300
closest p · 0.6× alpha
0.0300
boldest claim

The sentences

of borderline significanceP=0.03actually significant
29 , 42 The SEARCH genome-wide association study found no evidence for significant associations between other SLCO1B1 SNPs and simvastatin-induced myopathy, but in haplotypes with rs4149056 there was an association of borderline significance (P=0.03) between the G allele of the functional variant rs2306283 (c.388A>G) and lower risk of myopathy. 8 The effect of the rs2306283 polymorphism on the transport function of OATP1B1 is variable in different studies and may be substrate-specific. 44 In some studies it has been found to be associa

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