Association between single nucleotide polymorphisms in ERCC4 and risk of squamous cell carcinoma of the head and neck.

PLoS One · 2012 · PMC3407112 · PMID 22848636

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borderline significantno p-value reported

We found that the variant GG genotype of rs2276466 was significantly associated with a decreased risk of SCCHN (OR = 0.69, 95% CI 0.50–0.96), and that the variant TT genotype of rs3136038 showed a borderline significant decreased risk with SCCHN (OR = 0.76, 95% CI: 0.58–1.01) in the recessive model.

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