Table 2.

Mean number of causal variants detected in top r ranked SNPs given by each method on different sample sizes at relative risk 1.25

Sample size	Mean r	χ2	SVM(2r)	RF(2r)
2000	2.1	1.2	1.2	1.2
4000	9.2	4.8	5.7	4.4
8000	31.7	11.0	12.1	8.5