TABLE 6.
Power of the association test based on the statistic Tgene assuming two interacting disease loci within one gene under different sample sizes and different simulation schemes
MS program
|
LD based (r2 = 0.9)
|
||||
---|---|---|---|---|---|
Disease model | (BL, GE) | n = 200 | n = 400 | n = 200 | n = 400 |
Model 1 | (1, 0.7) | 0.379 (0.160) | 0.564 (0.385) | 0.816 (0.709) | 0.994 (0.822) |
(1, 0.9) | 0.708 (0.272) | 0.874 (0.595) | 0.909 (0.817) | 1.000 (0.827) | |
Model 2 | (1, 0.7) | 0.269 (0.152) | 0.455 (0.387) | 0.468 (0.349) | 0.835 (0.641) |
(1, 0.9) | 0.458 (0.232) | 0.658 (0.559) | 0.621 (0.426) | 0.938 (0.733) |
The power for the single SNP analysis is given in parentheses. BL, baseline effect; GE, genotypic effect. For the MS program, we set the fourth and ninth SNPs as the two interacting loci. For the LD-based simulation, we simulate two LD blocks, one containing six SNPs and the other containing four SNPs, with pairwise r2 = 0.9 for SNPs within each block. Two interacting disease loci are from each block with allele frequency PD = 0.3. The significance level is 0.05. Models 1 and 2 are defined in Table 3.