Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution

Figure 3

The distribution of variants in 60 patients with hyperbilirubinemias. Variants in UGT1A1 regulatory regions are shown as nucleotide changes. Variants in the UGT1A1 coding region are shown as amino acid substitutions. Novel variants are indicated in red.