Fig. 3From: A comprehensive comparison of multilocus association methods with summary statistics in genome-wide association studiesEstimated power for the seven SNP-set methods in the case of rare variant association study under the sparse case with a significance level α of 10−5. Here, PVE = 0.3%, 0.5% or 1% at the right side, the number of causal SNPs = 0.05, 0.20 or 0.50 on the top, the number of the total analyzed SNPs = 50, 200 or 500 on the x-axis. The power was estimated across 103 replicationsBack to article page