Barely Significant
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FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population.

Breast Cancer Res Treat · 2017 · PMC5645429 · PMID 28702895

2
hedged sentences
0.0002
closest p · 0.0× alpha
0.0002
boldest claim

The sentences

highly significantP = 0.0002actually significant
Highly significant association was seen between breast cancer and carrying either of the mutations (OR 1.86, 95% CI 1.32–2.49, P = 0.0002).

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In addition, the breast cancer risk was increased also in the other subgroups, e.g., ER negative (OR 2.34, 95% CI 0.75–7.35, P = 0.14) and familial breast cancer (OR 2.50, 95% CI 0.83–7.51, P = 0.10) (Table 2 ), but the results did not reach statistical significance.

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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.