Barely Significant
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Association of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study.

PLoS One · 2011 · PMC3246501 · PMID 22216261

Europe PMCDOI
1
hedged sentence
0.0270
closest p · 0.5× alpha
0.0270
boldest claim

The sentences

marginally significantp = 0.027actually significant
In Mixed Ancestry individuals, who were successfully genotyped for both the GSTT1 and GSTT2B deletions, 13 of 414 controls (0.031) and 16 of 217 cases (0.074) were homozygous for both deletions (genotype Del-Del / Del-Del ), which was a marginally significant difference (p = 0.027).

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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.