CCND1 and metabolic syndrome: Patients with dyslipidemia had a significantly higher frequency of the NR3C1 Bcl1 G allele (dyslipidemia, 25, nondyslipidemia, 23) than in those with the CC genotype (dyslipidemia, 19, nondyslipidemia, 59) (P = 0.001) (Table 3).