genome-wide significant SNPs associated_with EUR

additional approximately 0.24% (P = 8.7 × 10−55) of phenotypic variance in EUR above what is explained by the VNTR alone

more than 85% of GWS SNPs detected in the non-EUR groups are in strong LD (rLD2 > 0.8) with at least one variant reaching marginal genome-wide significance in EUR

increasing the sample size from 2.5 million to 4 million by adding another 1.5 million EUR samples increased the number of GWS SNPs from 7,020 to 9,863