Barely Significant
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Common Variants for Heart Failure.

Curr Genomics · 2015 · PMC4467308 · PMID 26085806

Europe PMCDOI
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hedged sentence
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closest p · 0.0× alpha
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The sentences

showed a trendP=8.8*10(-6)actually significant
No polymorphisms with genome-wide levels of significance (P<5*10(-7)) were identified, although rs740363 showed a trend for association with HF(P=8.8*10(-6)) [ 5 ].

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