Even so, it is noteworthy the relatively homogeneous molecular base of the G6PD deficiency found in the analysed sample of Venezuelan population, contrasting with the high heterogeneity reported in several studies that revealed a substantial number of G6PD variants in LA populations, such as the G6PD A-376G/968C, G6PD Santamaría376G/542T, G6PD Seattle844C, G6PD Mediterranean563T, and G6PD Union1360T described in Mexico, Brazil and Cuba [20–22]. The gene discussed is G6PD; the disease is G6PD deficiency.