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If none of them are available, you might use data from the 1000 Genomes Project (you will need PLINK2 --vcf option to convert the data into PLINK binary PED format).

Please see Figure 1 of Bakshi et al. 2016 for a comparison of results using different reference sets for LD. This can be from a standard GWAS or from a meta-analysis. For example, you can create a SNP set which contains all the 1KGP SNPs in genes involved in a pathway listed in the file below.