Barely Significant
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Association of XRCC1 p. Arg194Trp gene polymorphism with the risk of hepatocellular carcinoma in HCV Egyptian population: A pilot case-control study.

Int J Immunopathol Pharmacol · 2024 · PMC11189007 · PMID 38898405

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did not reach statistical significancep -values >0.05actually significant
The frequency of the T allele was higher among HCC participants (32%) compared to those with cirrhosis (23.5%) and carrying the T allele increased the risk of HCC by 1.532 times, however, these associations did not reach statistical significance ( p -values >0.05).

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