Fig. 2From: Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing dataMapping precision of GWAS based on different genotyping strategies. Results are from 50,000 simulations for causal common (a) and rare (b) variants, respectively, based on the UK10K-WGS data. Shown on the y-axis is the proportion of causal variants that were mapped to variants within a certain distance as specified on the x-axisBack to article page