Abstract: The interaction of rs2299939 variant genotypes (GT+TT) with
A3054T mutation significantly increased
HCC risk (AOR = 2.41, 95% CI = 1.08-5.35); whereas its interaction with
C3116T mutation significantly reduced
HCC risk (AOR = 0.34, 95% CI = 0.18-0.66).
Result: Although the variant genotype of rs2299939 was significantly associated with a reduced risk of
HCC, the interaction of rs2299939 variant genotypes with
A3054T was significantly associated with an increased risk of
HCC.