Groundbreaking discoveries in the human genome along with advances in nextgeneration sequencing (NGS) technologies made the study of inherited cardiovascular conditions (ICCs) more powerful than ever. The increased availability of genetic testing potentiates the opportunity of early detection of ICC, enabling a multidisciplinary genetic team to provide timely care to patients and families. Additionally, recent advances in gene modulation through sophisticated techniques set the stage for a new era in therapeutics and translatability from bench-to-bedside. Although the benefits of cardiogenetics are evident, most fellows receive neither scarce exposure nor acquisition of tools to assess risk potential of such diseases.1

Despite the absence of a standardised training curriculum, multiple pathways to a career in cardiogenetics coexist (figure 1).2 The heterogeneity and complexity of ICC demands acquaintance in diverse areas of cardiology, including arrhythmias, heart failure, cardiovascular imaging (echocardiography, CT, MRI), preventive cardiology and paediatric cardiovascular medicine.3 Essential competencies for clinical practice, such as interpretation of genetic test results and polygenic risk scores, genotype–phenotype correlations, construction of pedigrees and familiarity with …