Maverick Variant Pathogenicity Data Resources

<p>MAVERICK is a Mendelian Approach to Variant Effect pRedICtion built in Keras. It classifies protein-altering variants as either dominant disease-causing, recessive disease-causing, or benign. Here, we provide the pre-computed scores for all missense and nonsense SNVs in Gencode Basic V33 on GRCh37 and lifted over to GRCh38 as well as the datasets on which MAVERICK was trained and primarily evaluated.&nbsp;</p>