Aside from ABC transporters (ABCC1, ABCC2, ABCC5, ABCB1, ABCB4), genetic variants of NOS3 [74], CBR3 [76,77], cytochrome B-245 alpha chain (CYBA) [78], GST protein 1 (GSTP1) [79], hydroxysteroid sulfotransferase 2B1 (SULT2B1) [80], p450 oxidoreductase (POR) [81], organic anion transporters (solute carrier family 22 members 7 and 17 (SLC22A7 and SCL22A17) and SLC family 8 member 3 (SLC28A3)) [80], iron-metabolism-regulating protein (human hemochromatosis (HFE)) [82], and retinoic acid receptor-gamma (RARG) [57] were associated with ACT. Here, RARG is linked to hemochromatosis type 1.