Table 2.
Associations of ODC genotypes with risk of adenoma recurrence, Aspirin/Folate Polyp Prevention Study, 1994–2001
| SNP | Positiona | Location | Call rate | PHWE | MAF | RR (95% CI)c | P | Qd |
|---|---|---|---|---|---|---|---|---|
| rs13000916 | 10490304 | 3’ flanking | 0.995 | 0.09 | 0.449 | 0.89 (0.80–0.99) | 0.031 | 0.07 |
| rs11694911 | 10490649 | 3’flanking | 0.991 | 0.96 | 0.106 | 1.29 (1.10–1.51) | 0.002 | 0.027 |
| rs2430419 | 10493239 | 3’flanking | 1.000 | 0.59 | 0.247 | 1.09 (0.97–1.24) | 0.15 | 0.27 |
| rs2430420 | 10493677 | 3’flanking | 1.000 | 0.86 | 0.324 | 1.17 (1.05–1.31) | 0.005 | 0.027 |
| rs10929669 | 10493883 | 3’flanking | 0.997 | 0.61 | 0.115 | 1.22 (1.04–1.43) | 0.017 | 0.054 |
| rs28362434 | 10496095 | 3’flanking | 1.000 | 0.82 | 0.183 | 0.94 (0.81–1.08) | 0.36 | 0.52 |
| rs818162 | 10496675 | 3’flanking | 1.000 | 0.44 | 0.302 | 0.86 (0.76–0.97) | 0.012 | 0.048 |
| rs1049500 | 10498418 | Exon 12b | 1.000 | 0.57 | 0.041 | 1.38 (1.10–1.73) | 0.005 | 0.027 |
| rs28362416 | 10498720 | Intron 11 | 0.996 | 0.10 | 0.067 | 0.85 (0.67–1.07) | 0.18 | 0.29 |
| rs7559979 | 10500130 | Intron 8 | 0.985 | 0.61 | 0.347 | 1.05 (0.93–1.17) | 0.44 | 0.59 |
| rs28362380 | 10504231 | Intron 1 | 0.999 | 0.83 | 0.103 | 1.04 (0.88–1.23) | 0.67 | 0.77 |
| rs2302615e | 10505589 | Intron 1 | 0.998 | 0.50 | 0.254 | 1.02 (0.90–1.15) | 0.80 | |
| rs1728148 | 10508908 | 5’ flanking | 0.999 | 0.79 | 0.451 | 0.92 (0.83–1.02) | 0.12 | 0.24 |
| rs885815 | 10509079 | 5’ flanking | 0.992 | 0.32 | 0.214 | 0.96 (0.84–1.09) | 0.51 | 0.63 |
| rs2884211 | 10509623 | 5’ flanking | 1.000 | 0.70 | 0.077 | 1.01 (0.83–1.23) | 0.89 | 0.94 |
| rs2357551 | 10509631 | 5’ flanking | 1.000 | 0.73 | 0.342 | 1.13 (1.01–1.27) | 0.029 | 0.07 |
Abbreviations: SNP, single nucleotide polymorphism; MAF, minor allele frequency; HWE, Hardy-Weinberg equilibrium; RR, relative risk; CI, confidence interval.
Location on chromosome 2p25 according to NCBI Human Genome Map Build 36.
The substitution is synonymous.
Per allele relative risk and Wald test p-value using an additive genetic model adjusted for age and sex
False-discovery rate Q-values (27).
Previously genotyped SNP, not included in multiple testing correction (n=765)(17).