The results suggested that TCL1A (PPH3+PPH4 = 59.65, 51.22, 64.99), TNFSF8 (PPH3+PPH4 = 68.62, 61.06, 71.63), WFDC1 (PPH3+PPH4 = 52.10, 65.62, 62.41), and TNFAIP8 (PPH3+PPH4 = 55.46, 53.92, 55.35) shared causal variants with AML across all three analyses (deCODE to FinnGen, deCODE to UK Biobank, and UKB-PPP to FinnGen, Figure 3). The gene discussed is TCL1A; the disease is acute myeloid leukemia.