Barely Significant
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The association of XRCC1 polymorphism with osteosarcoma risk, clinicopathologic features, and prognosis in a Chinese Han population.

Cancer Manag Res · 2018 · PMC6208551 · PMID 30464596

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

did not reach statistical significanceP >0.05actually significant
Under dominant, recessive, and additive models, a decreased risk of OS development could be observed in subjects carrying the A allele, but the difference did not reach statistical significance (all P >0.05).

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