In this subsetting, 22 variants in 15 genes associated with Brugada syndrome were identified in 21 patients (34%), including SCN5A, CACNA1S, CACNB2, CASQ2, DLG1, JUP, KCNE1, KCNH2, KCNJ5, KCNQ1, PKP2, SCN10A, DSP, MYBPC3, and LAMA2. The gene discussed is LAMA2; the disease is Brugada syndrome.