Barely Significant
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Clinical implications of germline mutations in breast cancer genes: RECQL.

Breast Cancer Res Treat · 2019 · PMC6439214 · PMID 30610487

Europe PMCDOI
1
hedged sentence
0.0430
closest p · 0.9× alpha
0.0430
boldest claim

The sentences

borderline significancep = 0.043actually significant
In a cohort of 1946 breast cancer cases, they observed six carriers of the missense variant c.468T > G (p.I156M) (0.3%), which was not identified in any of the 1408 controls tested, giving a borderline significance ( p = 0.043).

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