There were no statistically significant differences in the incidence of variants related to familial hypercholesterolemia (LDLR NM_001195800.2:c.667G>A, PCSK9 NM_182961.4:c.658−36G>A NM_174936.3:c.658−36G>A, and APOB NM_000384.3:c.12382G>A) between both cohorts. Here, PCSK9 is linked to familial hypercholesterolemia.