| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | UGT1A, UGT1A1
+8 more (R108C) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | |
| | UGT1A5, UGT1A6
+8 more (I370V +4 more) | Single nucleotide variant (missense variant) | Gilbert syndrome +1 more | |
| | UGT1A7, UGT1A8
+8 more (M123I +4 more) | Single nucleotide variant (missense variant) | Crigler-Najjar syndrome type 1 | |
| | UGT1A3, UGT1A4
+8 more (R135L +4 more) | Single nucleotide variant (missense variant) | Crigler-Najjar syndrome type 1 | |
Click to view in NCBI Gene