| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity; drug response; other |
| | UGT1A, UGT1A1
+8 more (R209W) | Single nucleotide variant (missense variant +1 more) | UGT1A1-related condition +4 more | GPathogenic/Likely pathogenic |
| | UGT1A1, UGT1A10
+8 more (R341* +4 more) | Single nucleotide variant (nonsense) | not provided +2 more | |
| | UGT1A9, UGT1A
+8 more (D356N +4 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
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