Barely Significant
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Common polymorphisms of protein tyrosine phosphate non-receptor type 2 gene are not associated with risk of Crohn's disease in Indian.

World J Gastrointest Pathophysiol · 2022 · PMC9350595 · PMID 36161231

Europe PMCDOI
2
hedged sentences
0.0700
closest p · 1.4× alpha
0.0700
boldest claim

The sentences

close to being statistically significantP = 0.07so close (0.05 < p ≤ 0.1)
Among patients who underwent surgery for CD in past, 28.6% had the variant genotype (GT or GG) while 50% of patients without prior surgery had this variant and the difference was close to being statistically significant ( P = 0.07).

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did not reach statistical significanceno p-value reported
The PTPN2 SNP rs7234029 GG or GA genotype was more common in patients with perianal disease and less common in patients with disease onset after 40 years although the difference did not reach statistical significance.

also in 111,027 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.