Ultrarapid drug metabolism mediated by CYP2D6 is associated with inheritance of alleles with duplicated or amplified functionalCYP2D6genes. However, genotyping for duplicatedCYP2D6alleles only explains a fraction (10–30%) of the ultrarapid metabolizer phenotypes observed in Caucasian populations. Using a sample ofCYP2D6duplication-negative ultrarapid metabolizer subjects and selected control subjects with extensive metabolism, we examined parts of theCYP2D7pseudogene, and the promoter region and 5′-coding sequence ofCYP2D6for polymorphisms possibly associated with the ultrarapid metabolizer phenotype. In an initial screening of 17 subjects (13 ultrarapid metabolizers and four extensive metabolizers), we identified three DNA variants in the 5′-end of theCYP2D7pseudogene and 29 variants in the 5′-end of theCYP2D6gene. Five variants were then selected for examination in a larger sample of subjects having the ultrarapid metabolizer (n= 27) or extensive metabolizer phenotype (n= 77). Subsequent statistical analyses of allele, genotype and estimated haplotype distributions showed that the 31A allele of the 31G > A (Val11Met) polymorphism was significantly more frequent in ultrarapid metabolizer subjects than in extensive metabolizer subjects (P= 0.04). Also, estimation of haplotype frequencies suggested that one of the haplotypes with the 31A variant was significantly more frequent among the ultrarapid metabolizers compared with the extensive metabolizers (P= 0.03). The average metabolic ratio was significantly lower in subjects possessing the 31A allele compared with subjects homozygous for the 31G allele (P= 0.02). We also observed a non-significant over-representation of the G-allele of a −1584 C > G promoter polymorphism in the ultrarapid metabolizer group. Since our results are based on a relatively low number of subjects, further studies on larger samples and functional analyses of the polymorphisms detected are necessary to determine the role of the 31G > A and −1584C > G variants inCYP2D6duplication-negative ultrarapid metabolizer subjects.