Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.

BMC Med Genet · 2011 · PMC3190329 · PMID 21957892

Europe PMC DOI

hedged sentence

0.0520

closest p · 1.0× alpha

0.0520

boldest claim

The sentences

of borderline significanceP = 0.052so close (0.05 < p ≤ 0.1)

The recessive A/A genotype was of borderline significance in an age- and race-adjusted analysis of the entire combined cohort (N = 3095; P = 0.052), but this finding was not confirmed in independent cohorts (N = 6086).

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