Barely Significant
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Pathogenic variants carrier screening in New Brunswick: Acadians reveal high carrier frequency for multiple genetic disorders.

BMC Med Genomics · 2022 · PMC9055701 · PMID 35488281

Europe PMCDOI
1
hedged sentence
0.1000
closest p · 2.0× alpha
0.1000
boldest claim

The sentences

a strong trendP < 0.1so close (0.05 < p ≤ 0.1)
One variant in USH2A , while not statistically significant, did show a strong trend for enrichment ( P < 0.1, Table 1 ).

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