Table 1.

Whole-genome sequencing (WGS) datasets

Study	Ancestry	Mean depth	Sample size		Number of variants in 2,429 samples used in analyses
			total	unrelated	bi-allelic		multi-allelic		total
					SNV	indel	SNV	indel
InPSYght22, 23, 24, 25, 26, 27	African	27	7,717	7,169	72.6M	1.3M	5.3M	0.2M	79.3M
BioMe18	Hispanic/Latino	37	4,677	3,141	63.2M	0.9M	4.5M	0.1M	68.8M
MLOF21	European	39	2,987	2,429	57.3M	0.8M	4.1M	0.1M	62.2M
METSIM19,20	Finnish	24	3,045	2,703	20.5M	0.1M	1.4M	10K	22.0M

The study name, ancestry, mean sequencing depth, sample size (total and unrelated subset), and number of variants, including single-nucleotide variants (SNVs) and indels, for the four WGS datasets.