We also performed a look-up of the nine validated SNV associations in the non-European samples. Due to the lack of power, and different allele frequencies compared with Europeans, none of the SNVs had results with P < 0.05 within any ancestry (Supplementary Material, Fig. S6), and there was little concordance in effect directions: 56% and P = 0.246 for AA; 33% and P = 0.164 for HIS and CH.
