Skip to main content
. 2022 Oct 12;2(10):100190. doi: 10.1016/j.xgen.2022.100190

Table 1.

Drug targets and representative drugs prioritized in this study

Disease Overlap enrichment in disease-relevant ATC codes Endophenotype MR Negative correlation tests
Asthma ibudilast (IL6); omalizumab (FCER1A/FCER1G); alicaforsen (ICAM1) SAR164653 (CTSA); KHK-2866 (HBEGF); amediplase (PLAU) donepezil (ACHE); vorinostat (HDAC family); BRD-K50748030 (unknown)
POAG LY-288513 (unknown)
Gout probenecid (SLC22A6/SLC22A11); lesinurad (SLC22A11/SLC22A12) anfibatide (GP1BA); berotralstat (KLKB1) mesoridazine (DRD2/HTR2A); CP-724714 (unknown)a
COPD GMA-161 (FCGR3B) BRD-K48950795 (unknown); RAN-29 (unknown)
VTE alteplase (FGA); edoxaban (F10); ancrod (PROC); dabigatran etexilate (F2); abelacimab (F11); ecallantide (KLKB1); drotrecogin alfa (F5) abelacimab (F11); CR-002 (PDGFB) WH-4025 (unknown)
ThC tosedostat (XPNPEP2) (excluded from the analysis)
AAA MG-1102 (LPA); amediplase (PLAU) (excluded from the analysis)
HF MG-1102 (LPA)
IPF
Stroke
UtC Anfibatide (GP1BA)
AcApp GNF-PF-5434 (CTSB) (excluded from the analysis)
HCM

The diseases are sorted in the decreasing order of the number of the genome-wide significant loci in GBMI GWAS.

a

Drugs without known target genes were not shown except for the drug with the lowest p value, CP-724714. Full results can be found in Table S2.