Barely Significant
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Chemokine receptor CXCR6 gene polymorphism and treatment response of chronic hepatitis C virus in Egyptian patients.

Clin Exp Hepatol · 2021 · PMC8977876 · PMID 35402715

Europe PMCDOI
2
hedged sentences
0.0030
closest p · 0.1× alpha
0.0030
boldest claim

The sentences

highly significantp = 0.003actually significant
Genotype GG was associated with significant increased risk of not responding to treatment by 4.25 times as compared with TT genotype ( p = 0.019) and the G allele was associated with highly significant risk of not responding to treatment by 2.56 times compared with the T allele ( p = 0.003).

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