Association statistics for thyroid cancer risk and genetic variants at chromosomes 5q24, 8q24, 9q22 and 14q13
| SNP, genotypes and risk allele | Frequency (%) | ORs for genotype or per allele overall (95% CI) | p Value | |
| Cases | Controls | |||
| rs2910164 | ||||
| GG | 436 (0.578) | 3540 (0.584) | Reference | |
| CG | 271 (0.367) | 2179 (0.360) | 1.032 (0.876 to 1.214) | 0.728 |
| CC | 41 (0.054) | 339 (0.056) | 0.987 (0.682 to 1.384) | 0.985 |
| Risk allele (C) | 359 (0.238) | 2857 (0.236) | 1.013 (0.893 to 1.148) | 0.845 |
| rs6983267 | ||||
| TT | 164 (0.218) | 1441 (0.236) | Reference | |
| GT | 346 (0.461) | 3012 (0.493) | 1.010 (0.827 to 1.236) | 0.960 |
| GG | 241 (0.321) | 1662 (0.272) | 1.274 (1.027 to 1.583) | 0.026 |
| Risk allele (G) | 674 (0.449) | 5894 (0.518) | 1.140 (1.025 to 1.268) | 0.016 |
| rs965513 | ||||
| GG | 187 (0.249) | 2748 (0.449) | Reference | |
| AG | 394 (0.525) | 2729 (0.446) | 2.121 (1.763 to 2.559) | 9.08×10−17 |
| AA | 170 (0.226) | 643 (0.105) | 3.883 (3.081 to 4.893) | 1.30×10−30 |
| Risk allele (A) | 734 (0.489) | 4015 (0.328) | 1.981 (1.774 to 2.212) | 6.35×10−34 |
| rs1867277 | ||||
| GG | 159 (0.211) | 2290 (0.376) | Reference | |
| AG | 398 (0.529) | 2879 (0.473) | 1.991 (1.638 to 2.428) | 3.99×10−13 |
| AA | 196 (0.260) | 918 (0.151) | 3.074 (2.446 to 3.864) | 5.97×10−23 |
| Risk allele (A) | 790 (0.525) | 4715 (0.387) | 1.749 (1.569 to 1.950) | 5.90×10−24 |
| rs944289 | ||||
| CC | 87 (0.116) | 1003 (0.164) | Reference | |
| CT | 332 (0.441) | 2924 (0.478) | 1.309 (1.019 to 1.582) | 0.033 |
| TT | 334 (0.444) | 2193 (0.358) | 1.755 (1.365 to 2.276) | 4.36×10−6 |
| Risk allele (T) | 1000 (0.664) | 7310 (0.597) | 1.330 (1.188 to 1.489) | 6.95×10−7 |
SNP, single nucleotide polymorphism.