Meta-analyses of the European ancestry genome-wide association study (GWAS) suggested that variants of rs3846663 in HMGCR, rs1501908 between TIMD4 and HAVCR1, rs2650000 near HNF1A, and rs6102059 near MAFB were associated with dyslipidemia [19]. The gene discussed is HAVCR1; the disease is metabolic syndrome.