Our analyses use summary statistics from GWASs conducted by 23andMe in samples of European-ancestry volunteer research participants for 37 different phenotypes. Supplementary Table 6 provides an overview of these summary statistics. 28 out of the 37 are from previously published studies5,42–55. For these, we cite the original study in the column labelled “Citation”. The remaining 9 are based on previously unreported GWASs. Two of these GWASs are for phenotypes (Subjective Well-Being and Risk) for which GWASs had been previously published by 23andMe but with a smaller sample. The remaining summary statistics have not been previously published by 23andMe. Supplementary Table 6 describes the details of the association model used for each phenotype. For details on 23andMe’s genotyping and imputation, see Supplementary Tables 17 and 18 in Lee et al.5
