SFTA1P and Behcet disease: Additionally, the analyses revealed that four genes (CENPQ, STK19B, HLA-DRB6, and GSTM3) and fourteen genes (ERAP2, NBR2, TRMT61B, LRRC37A4P, WFDC3, SFTA1P, MAPK8IP1P2, HLA-DOB, NPIPB2, DND1P1, AMH, LRRC37A2, ZNF589, and LRRC37A) were associated with a potentially increased risk of comorbidity between BD and MI (Supplementary Table S8) and between SCZ and MI (Supplementary Table S9), respectively.