BOL

You can try the following --

1. gnomAD (https://gnomad.broadinstitute.org/)
gnomAD v3, have 602M SNVs + 105M indels using whole-genome sequencing of 71,702 samples mapped to the GRCh38 build of the human reference genome.

2. DiscoverEHR (http://www.discovehrshare.com/)
exomes >50,000 MyCode® participants, have >4M rare SNV and indels