Thyroid cancer risk associated with different haplotypes, defined by rs965513 and rs1867277 alleles, at chromosome 9q22
| Haplotype | rs965513 | rs1867277 | Frequency | OR | p Value | |
| Cases | Controls | |||||
| 1 | G | G | 0.413 | 0.561 | Reference | |
| 2 | A | A | 0.429 | 0.276 | 2.139 (1.902 to 2.407) | 2.19×10−35 |
| 3 | A | G | 0.097 | 0.111 | 1.189 (0.978 to 1.485) | 0.077 |
| 4 | G | A | 0.061 | 0.052 | 1.612 (1.264 to 2.037) | 0.0001 |
Haplotype frequencies were estimated using Haploview (http://www.haploview.org/). Only samples with full data at both loci were used for the analyses (761 cases and 6085 controls).