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. 2013 Jul 23;54(5):1158–1167. doi: 10.3349/ymj.2013.54.5.1158

Table 1.

Frequency of NQO1 and NQO2 Polymorphisms in Nodular Hyperplasia and Papillary Thyroid Microcarcinoma

graphic file with name ymj-54-1158-i001.jpg

NQO1, NAD(P)H:Quinone Oxidoreductase 1; NQO2, NRH:Quinone Oxidoreductase 2; NH, nodular hyperplasia; PTMC, papillary thyroid microcarcinoma. C/C: wild type NQO1. C/T: heterozygote C609T missense variant of NQO1. I29: 29 basepair insertion polymorphism of NQO2. D: 29 basepair deletion polymorphism of NQO2.

*The NQO1 polymorphisms of 25 cases of 73 NH and 45 cases of 170 PTMC were not able to be assessed.

Two cases of PTMC showing the I29/I16 genotype were not included.

Pair-wise comparisons from the Pearson χ2 test.

§Comparisons of three or four groups using linear by linear association.