Barely Significant
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High prevalence of genetic variants previously associated with LQT syndrome in new exome data.

Eur J Hum Genet · 2012 · PMC3400735 · PMID 22378279

Europe PMCDOI
1
hedged sentence
0.0510
closest p · 1.0× alpha
0.0510
boldest claim

The sentences

borderline significantP =0.051so close (0.05 < p ≤ 0.1)
In this case, only a borderline significant difference was found ( P =0.051) for the overall comparison.

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