Barely Significant
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Genetic variants in <i>ATP2B2</i> as risk factors for mortality in patients unrelated but not associated with families with severe COVID-19.

Heliyon · 2024 · PMC11019202 · PMID 38628728

Europe PMCDOI
1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

showed a trendp = 0.06so close (0.05 < p ≤ 0.1)
In the same way, the genotype TC (rs767455) in TNFRSF1A showed a trend with a higher frequency in non-survivor patients (56.7 vs . 37.3, p = 0.06).

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