Table 2.

Statistically significant association between genotypes and risk of PTC among whites (n = 760)

ChromosomeGene nameSNPGenotypeCasesControlsOR (95% CI)P
7HUS1rs2708896GG991081
TG1711990.92 (0.65–1.30)0.641180875
TT631200.55 (0.36–0.83)0.004611807
Ptrend0.00570544
TG & TT2343190.78 (0.56–1.08)0.133937371
7HUS1rs10951937TT1261421
TG1611850.98 (0.70–1.35)0.886392195
GG461000.51 (0.33–0.79)0.002373343
Ptrend0.00704081
GG & TG2072850.81 (0.60–1.10)0.182937296
10MGMTrs12769288CC2763171
TC551010.62 (0.43–0.90)0.012889857
TT290.23 (0.05–1.10)0.065342142
Ptrend0.0023066
TC & TT571100.59 (0.41–0.85)0.004426897