Barely Significant
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The Genetic Variability of Members of the SLC38 Family of Amino Acid Transporters (<i>SLC38A3</i>, <i>SLC38A7</i> and <i>SLC38A9</i>) Affects Susceptibility to Type 2 Diabetes and Vascular Complications.

Nutrients · 2022 · PMC9654215 · PMID 36364703

Europe PMCDOI
2
hedged sentences
0.0760
closest p · 1.5× alpha
0.0760
boldest claim

The sentences

borderline significantp = 0.076so close (0.05 < p ≤ 0.1)
Yet, a borderline significant decreased risk of T2D was observed for SNPs rs731710-A/G ( SLC7A5 ) and rs3783436-T/C ( SLC7A8 ) under a dominant model (OR = 0.73, 95% CI: 0.51–1.03; p = 0.076 and OR = 0.70, 95% CI: 0.48–1.04, p = 0.078, respectively). 3.3.

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nominally significantno p-value reported
We did not find any evidence of nominally significant genotype-phenotype association when the variability of rs1858828 genotypes was analyzed with respect to the anthropometric and biochemical parameters, both in diabetic and non-diabetic individuals.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.