To access the data, click or select the words “Appendix 2.” Variants not found in the 1000Genomes, EVS6500, dbSNP v138 or ExAC databases that occurred in >1 sequenced case but no controls (i) or >1 controls and no cases (ii) where a) shows all exonic variants predicted to be damaging, and b) the most frequently observed variants (by allele count).