Table 3.

Mean number of causal variants detected in top r ranked SNPs by each method on data with causal allele frequencies at most 5% and two different sample sizes and relative risks

Sample size and relative risk	χ2	SVM(2r)	RF(2r)
4000, 1.25	0.5	1	1
8000, 1.25	1.7	2.5	2.5
4000, 1.5	4.8	6.3	6.1
8000, 1.5	12.7	13.2	13.3