The contribution of a 9p21.3 variant, a KIF6 variant, and C-reactive protein to predicting risk of myocardial infarction in a prospective study.

BMC Cardiovasc Disord · 2011 · PMC3066109 · PMID 21406102

Europe PMC DOI

hedged sentence

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closest p · 1.6× alpha

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boldest claim

The sentences

did not reach statistical significanceP = 0.08so close (0.05 < p ≤ 0.1)

After adjustment for the FRS risk factors, the risk allele (G) of the 9p21.3 SNP (rs10757274) was associated with increased risk of MI among white men (HR = 1.22; 95%CI 1.03 to 1.45, P = 0.02), this association did not reach statistical significance among white women (HR = 1.16; 95%CI 0.98 to 1.37, P = 0.08).

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