LDLR and familial hyperaldosteronism: Although they were identified in FH patients, p.(Gln378Pro), p.(Ala399Thr), p.(Thr413Met), p.(Ala606Ser), p.(His656Asn) and p.(Thr659Asn) LDLR variants were found to be non-pathogenic thereby indicating that the variants do not account for the clinical presentation.