Barely Significant
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Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes.

Biomedicines · 2020 · PMC7601281 · PMID 33050356

Europe PMCDOI
1
hedged sentence
0.0510
closest p · 1.0× alpha
0.0510
boldest claim

The sentences

marginally insignificantp = 0.051so close (0.05 < p ≤ 0.1)
The frequencies of germline mutations in CHEK2 gene ( Supplementary Figures S1 and S2 ), BRCA1 , and MUTYH were three times higher in patients over controls but marginally insignificant (all p = 0.051; Supplementary Table S4 ). 3.1.4.

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