Through a phenome-wide scan of multiple publicly available sources, we observed associations between SLC22A24 and conotruncal heart defect (p = 1x10-6)[77], lipid levels, and cardiovascular disease (p-values range from 1x10-5 to 9x10-5, data source Phenotype-Genotype Integrator, https://www.ncbi.nlm.nih.gov/gap/phegeni). Here, SLC22A24 is linked to Conotruncal defect.