Barely Significant
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Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium.

PLoS Genet · 2010 · PMC2891809 · PMID 20585626

Europe PMCDOI
3
hedged sentences
0.1200
closest p · 2.4× alpha
0.1200
boldest claim

The sentences

borderline significanceP = 0.12not close (p > 0.1)
Although the positive association with rs3803662 remained, it was of only borderline significance ( P = 0.12).

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highly significantno p-value reported
The association of this SNP with breast cancer risk remained highly significant in Asians after adjusting all previously-reported SNPs in this region.

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marginally significantno p-value reported
Three other SNPs also showed a significant or marginally significant association with breast cancer risk.

also in 26,082 other papers

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.