Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation.
Yuya KobayashiShan YangKeith NykampJohn GarciaStephen E LincolnScott E TopperPublished in: Genome medicine (2017)
The observations made in this study suggest that, with certain caveats, a very low allele frequency threshold can be adopted to more accurately interpret sequence variants.