| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity; drug response; other |
| | UGT1A, UGT1A5
+8 more (R341* +4 more) | Single nucleotide variant (nonsense) | Gilbert syndrome +2 more | |
| | UGT1A5, UGT1A6
+8 more (P361L +4 more) | Single nucleotide variant (missense variant) | Hyperbilirubinemia +7 more | GConflicting classifications of pathogenicity; other |
Click to view in NCBI Gene