Table 1 provides demographic information for this cohort. All patients were adults with a median age of 31 years, and 75% of them were female. All had VTs induced during clinical EPS, where information about the patients’ VTs were recorded. Genetic testing for ARVC risk variants was performed for the entire cohort. Eight patients were found to have PKP2 loss-of-function variants, while the remaining eight did not test positive for variants in any of the known causal genes and were thus considered gene-elusive (GE; James et al., 2021). Here, PKP2 is linked to Arrhythmogenic right ventricular dysplasia.