Barely Significant
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Genetic variation in 15-hydroxyprostaglandin dehydrogenase and colon cancer susceptibility.

PLoS One · 2013 · PMC3661460 · PMID 23717544

Europe PMCDOI
1
hedged sentence
0.0008
closest p · 0.0× alpha
0.0008
boldest claim

The sentences

highly significantp = 0.0008actually significant
While rs2555639 was the only SNP that was significantly associated with risk of colon cancer in each of the discovery and validation sets independently, several additional SNPs had highly significant association with risk when combining data from the discovery and validation samples ( Table 5 ), including rs1365611 (OR = 1.73, 95%CI:1.26–2.37, p = 0.0008), rs6844282 (OR = 1.42, 95%CI:1.10–1.83, p = 0.0078), and rs2332897 (OR = 1.74, 95%CI:1.27–2.38, p = 0.0006).

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