Dear gnomAD enthusiasts,
We are happy to announce the release of v3.1.1. This release contains some minor variant annotation corrections and changes to the v3.1 data release. To read the full description of the corrections and changes, check the gnomAD changelog. The major annotations, including allele count, allele number, and allele frequency, as well as variant filtering status, remain unchanged for the entire callset and for all subsets of the callset (except for a minor change in the representation of absent variants noted in the readme).
If you have any questions or feedback on the latest release please contact us at our email address: gno...@broadinstitute.org.
Happy Exploring,
The gnomAD Production Team