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Mapping precision of GWAS as measured by the squared LD correlations between causal variants and GWAS top SNPs 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 with LD r 2 smaller than a certain threshold as specified on the x-axis
