Barely Significant
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Unraveling genotype-phenotype relationships in hereditary hemochromatosis through integrated biobank data analysis.

BMC Genomics · 2026 · PMC13104239 · PMID 41840493

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

The sentences

nominally significantp < 0.05actually significant
Six of the 23 clinical symptom categories showed nominally significant differences between the carrier and control groups ( p < 0.05, chi-squared test).

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