Common variation in ISL1 confers genetic susceptibility for human congenital heart disease.

PLoS One · 2010 · PMC2877111 · PMID 20520780

Europe PMC DOI

hedged sentences

0.0007

closest p · 0.0× alpha

0.3590

boldest claim

The sentences

highly significantP = 0.0007actually significant

Rs1017 was highly significant in a log additive model, with an 81% increase in risk associated with each additional copy of the T allele (OR = 1.81, 95% CI 1.29–2.54, P = 0.0007).

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did not reach statistical significanceP = 0.359not close (p > 0.1)

Similarly, the G-C-T haplotype did not reach statistical significance among blacks/African Americans in stage 2, but the relative risk for this haplotype was consistent with that seen in stage 1 (OR = 1.28, 95% CI 0.75–2.19, P = 0.359).

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.