Barely Significant
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Exploring the genetic basis of essential hypertension: association with AGT gene variants in an Iranian population.

BMC Genomics · 2025 · PMC12750650 · PMID 41315929

Europe PMCDOI
1
hedged sentence
0.0610
closest p · 1.2× alpha
0.0610
boldest claim

The sentences

borderline significantp = 0.061so close (0.05 < p ≤ 0.1)
The C allele of rs2004776 also showed a borderline significant association (OR = 1.15, 95% CI: 0.99–1.33, p = 0.061, FDR = 0.020; Table 2 ).

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