Abstract 15371: Prevalence and Electronic Health Record-Based Phenotype of Loss-Of-Function Genetic Variants in Arrhythmogenic Cardiomyopathy-Associated Genes in 61,000 Individuals

Introduction: Arrhythmogenic cardiomyopathy (ACM) is associated with genetic variants in desmosome genes. Incidental findings of pathogenic/likely pathogenic (P/LP) variants in these genes, primari...