Fig. 1From: Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing dataDifferences in MAF between GWAS hits and causal variants for different genotyping strategies. Results are from 50,000 simulations based on the UK10K-WGS data for common (a) and rare (b) causal variants, respectively. Shown on the y-axis is the proportion of causal variants that were mapped to variants with MAF differences smaller than a value specified on the x-axisBack to article page