According to the HGMD, ClinVar, gnomAD, and LOVD databases, other LDLR variants at the same position, e.g., p.Glu179Lys, p.Glu179X, and p.Glu179Gly, have also been reported to cause FH in Italy, France, and Norway, respectively. The gene discussed is LDLR; the disease is familial hyperaldosteronism.