Fig. 2From: H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promotersFrequency of H558R in the BrS cases with or without VF history, The G allele (H558R) was not observed in BrS patients with a history of VF (P = 0.03)Back to article page