Several SNPs associated with FH were annotated in members of the LAC family, including psu.G.00002202 (LAC9), psu.G.00002203 (LAC5), and psu.G.00013272 (LAC17) (Supplementary Data Fig. S8B, Supplementary Data Table S12). The gene discussed is LCT; the disease is familial hyperaldosteronism.