Barely Significant
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Heterozygosity mapping for human dominant trait variants.

Hum Mutat · 2019 · PMC6617796 · PMID 31018026

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

highly significantp < 0.05actually significant
None of the H max values furnished significant results ( p < 0.05) while several H values were highly significant: In family S, all individuals carrying the pathogenic BRCA2 mutation (“carrier” in Table S1) show p < 0.05 for their H values and all noncarriers show p > 0.10.

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