| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | UGT1A3, UGT1A9
+8 more (L15R) | Single nucleotide variant (missense variant +1 more) | Crigler-Najjar syndrome, type II +4 more | |
| | UGT1A, UGT1A1
+8 more (K139fs +4 more) | Deletion (frameshift variant) | not provided +1 more | |
Click to view in NCBI Gene