Barely Significant
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The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetes.

BMC Med Genet · 2011 · PMC3072937 · PMID 21429197

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

The sentences

borderline significantp = 0.05actually significant
Furthermore, the CT and TT genotype carriers had a borderline significant higher proinsulin/C-peptide ratio in comparison with the CC genotype carriers (est.: 1.25, p = 0.05).

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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.