A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes

A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes. Joseph Park AB, Michael G. Levin MD, Christopher M. Haggerty PhD, Dustin N. Hartzel BS, Renae Judy MS, Rachel L. Kember PhD & Nosheen Reza MD Regeneron Genetics Center, Marylyn D. Ritchie PhD, Anjali T. Owens MD, Scott M. Damrauer MD & Daniel J. Rader MD.