Table 1. Spurious association rates in the exome data.
PC1 | |||||||
PC2 | OR 1/5 Fourth | OR 1/5 Half | OR 1/5 Full | OR 1 | OR 5 Full | OR 5 Half | OR 5 Fourth |
OR 1/5 Fourth | 0.0686 | 0.0548 | 0.0448 | 0.0400 | 0.0421 | 0.0501 | 0.0660 |
OR 1/5 Half | 0.0683 | 0.0543 | 0.0442 | 0.0402 | 0.0425 | 0.0521 | 0.0680 |
OR 1/5 Full | 0.0686 | 0.0544 | 0.0441 | 0.0397 | 0.0443 | 0.0524 | 0.0684 |
OR 1 | 0.0700 | 0.0555 | 0.0442 | 0.0389 | 0.0434 | 0.0527 | 0.0707 |
OR 5 Full | 0.687 | 0.0522 | 0.0434 | 0.0391 | 0.0454 | 0.0541 | 0.0684 |
OR 5 Half | 0.0683 | 0.0530 | 0.0441 | 0.0395 | 0.0444 | 0.0530 | 0.0689 |
OR 5 Fourth | 0.0641 | 0.0494 | 0.0401 | 0.0393 | 0.0448 | 0.0539 | 0.0667 |
The values are the average spurious association rate for ten run using 1,000 cases and controls from the European Americans in the Exome Sequencing Project. These are the rates at the 5% significance threshold for parameters defined as odds ratios (ORs) of 1/5, 1, or 5 for a fourth, half, or full distance between the minimum and maximum for each axis: PC1 are the columns, and PC2 are the probabilities calculated for each individual. Smaller values indicate larger differences in disease risk among individuals in PC space.