Barely Significant
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Gene Polymorphisms of NOD2, IL23R, PTPN2 and ATG16L1 in Patients with Crohn's Disease: On the Way to Personalized Medicine?

Genes (Basel) · 2021 · PMC8227795 · PMID 34198814

Europe PMCDOI
1
hedged sentence
0.0640
closest p · 1.3× alpha
0.0640
boldest claim

The sentences

near-significantp = 0.064so close (0.05 < p ≤ 0.1)
In addition, we found a near-significant association of the NOD2 rs2066844 risk allele with a history of IBD-related surgery (65.2% vs. 52.8%, p = 0.064; or, if corrected to the number of operations per disease year, 0.05 vs. 0.03, p = 0.091).

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