Barely Significant
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Hereditary α-Tryptasemia and Peripheral Blood <i>KIT</i> D816V Mutation in Patients with Pediatric Mastocytosis.

Int J Mol Sci · 2025 · PMC12249517 · PMID 40649802

Europe PMCDOI
1
hedged sentence
0.0530
closest p · 1.1× alpha
0.0530
boldest claim

The sentences

a positive trendp = 0.053so close (0.05 < p ≤ 0.1)
The analysis showed that only the presence of cutaneous symptoms is a significant positive predictor of BST; there was also a positive trend for the KIT p.D816V mutation ( p = 0.053). 3.

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