Table 1.
Study | Cases | Controls | Highest LOD score on chr. 1 case-only | Highest LOD score on chr. 1 cases + controls | Highest case–control Z-score on chr. 1 | Empirical p-value for admixture association | 95% CI for risk per European chromosome |
---|---|---|---|---|---|---|---|
2005 study | 605 | 1043 | 5.2 | 5.2 | 3.3 | N/A | 1.27–1.70 |
2007 follow-up | 1044 | 1161 | 9.2 | 9.3 | 4.2 | < 0.001 | 1.32–1.62 |
Full new cohort | 1305 | 1155 | 3.9 | 2.7 | 3.4 | 0.114 | 1.16–1.43 |
2007 subset of new cohort | 899 | 1155 | 9.8 | 9.3 | 4.5 | < 0.001 | 1.37–1.76 |
Samples added after 2007 | 406 | 1155 | − 3.6 | − 3.0 | 0.9 | 1 | 0.59–0.91 |
The highest LOD score results are computed by ANCESTRYMAP based on a prior on relative risk per European ancestry allele of 1.5. The 95% confidence intervals for risk per European allele are obtained by running on a uniformly spaced grid of models from 0.5 to 2.0-fold per European allele, assuming an equal prior probability of risk for each, and then taking the LOD score to the power of 10 and normalizing to obtain a posterior. The LOD scores for the grid of models for the 2005 study are from the original publication11; all LOD scores are given in Supplementary Table S3. Empirical p-values were found through permutation analysis; see “Materials and methods” section. p-values were listed as < 0.001 when 0 of the 1000 permutations had a score at least as large as that of the LOD score of that data subset.