Genetic variations in and genes are associated with lung cancer risk in a Chinese Han population.

The study was aimed to explore whether the and polymorphisms are associated with the lung cancer risk. Five and polymorphisms were genotyped from 554 lung cancer patients and 603 healthy controls. We used χ test, genetic model, linkage disequilibrium (LD) and haplotype analyses to evaluate the association between the polymorphisms and lung cancer risk. We found that the allele "C" of rs10936599 () and the allele "T" of rs10069690 () were associated with increased risk of lung cancer (OR = 1.32, 95% CI: 1.12-1.55, = 0.001; OR = 1.41, 95% CI: 1.14-1.76, = 0.002, respectively). The genotype of "CC" of rs10936599, genotype "CT" of rs10069690 and genotype "GG and "AG" of rs2853677 were also associated with increased the risk of lung cancer. In addition, rs10936599 under the dominant, recessive and log-additive models; rs10069690 under the dominant, overdominant and log-additive models; rs2853677 under the dominant and log-additive models were found to be associated with increased lung cancer risk. The SNP rs2242652 was found to be associated with an increased lung cancer risk under the dominant and overdominant models without adjustment. The haplotype "TA" of was also associated with an increased risk of lung cancer. Our study indicated that rs10936599 () and rs10069690, rs2242652 and rs2853677 in and haplotype "TA" of were revealed as risk factors of lung cancer in a Chinese Han population. However, it required to verify our result and investigate the function genetic variants and mechanism of lung cancer.