Single nucleotide polymorphisms associated with colorectal cancer susceptibility and loss of heterozygosity in a Taiwanese population.

We used permutation method (bootstrap n = 1,000) to adjust the p-values, and rs4631962 (adjusted p-value = 0.043) and rs1338565 (adjusted p-value = 0.015) showed marginal significance of allele frequency differences between 705 cases and 1,802 controls ( Table 1 ).

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