“…Of particular interest in the context of this review are works in which the NOS1, NOS2, and NOS3 genes SNVs were considered as risk factors for several comorbid disorders, including AH and M or associated conditions. + [23] rs2779249 - [11,12] +* [11] + [26,27] - [25] +* [25,26] rs2297518 - [11,12] +* [11,12] + [25,27] - [26] +* [25,26] NOS3 rs148554851 - [18] -* [18] rs1799983 + [13,17,20] - [8,10,12,14,15,18] -* [14,15,18] + [30,34] ± [24] - [28,29,[31][32][33]35] +* [30,32]-* [31] rs1800779…”