| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | UGT1A, UGT1A1
+8 more (G276R) | Single nucleotide variant (missense variant +1 more) | Crigler-Najjar syndrome, type II | |
| | UGT1A, UGT1A5
+8 more (R341* +4 more) | Single nucleotide variant (nonsense) | Gilbert syndrome +2 more | |
| | UGT1A10, UGT1A3
+8 more (Y486D +4 more) | Single nucleotide variant (missense variant) | Crigler-Najjar syndrome type 1 +6 more | GPathogenic/Likely pathogenic |
| | UGT1A, UGT1A1
+8 more (R255* +4 more) | Single nucleotide variant (nonsense) | Crigler-Najjar syndrome +1 more | |
Click to view in NCBI Gene