Table 2.
SNP | Coded allele | Position on chromosome 2 (NCBI build 37) | European Americans (N=711 cases and 6,384 controls) | African Americans (N=1,293 cases and 2,369 controls) | Meta-analysis | |||||
---|---|---|---|---|---|---|---|---|---|---|
Coded allele frequency (%) | P | OR (95% CI) | Coded allele frequency (%) | P | OR (95% CI) | P | OR (95% CI) | |||
rs7597593 | T* | 185,533,580 | 38.9 | 0.016 | 1.15 (1.03–1.29) | 63.8 | 0.67 | 0.98 (0.89–1.08) | 0.088 | 1.05 (0.97–1.13) |
rs1344706 | A | 185,778,428 | 61.1 | 0.029 | 1.14 (1.01–1.29) | 91.5 | 0.27 | 1.10 (0.93–1.32) | 0.016 | 1.13 (1.02–1.25) |
CI, confidence interval; OR, odds ratio
T is the complementary allele to the A allele reported by Sun et al. (in press).