Sudden Unexpected Death in Epilepsy (SUDEP) is the leading cause of premature mortality in epilepsy. Genetic cardiac risk factors, including loss-of-functionKCNH2variants, have been linked to SUDEP. We hypothesised that seizures and LQTS interact to increase SUDEP risk. To investigate this, we crossedKcnh2+/-andGabrg2R43Q/+mice that model LQTS and genetic epilepsy, respectively. Electrocorticography and electrocardiogram confirmed thatKcnh2+/-mice had a LQTS phenotype, whileGabrg2R43Q/+mice displayed spontaneous seizures. Double mutant mice (Kcnh2+/-/Gabrg2R43Q/+) had both seizure and LQTS phenotypes that were indistinguishable from the respective single mutant mice. Survival analysis revealed thatKcnh2+/-/Gabrg2R43Q/+mice experienced a disproportionate higher rate of seizure-related death. Long-term oral administration of atenolol, a cardiac-selective β-blocker, significantly improved survival in theKcnh2+/-/Gabrg2R43Q/+mice. Overall, the data implicates loss-of-functionKCNH2variants as an important risk factor, and the potential repurposing of β-blockers as a prevention strategy, for SUDEP in a subset of epilepsy patients.