| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | UGT1A, UGT1A1
+8 more (R108C) | Single nucleotide variant (missense variant +1 more) | Hyperbilirubinemia +4 more | |
| | UGT1A, UGT1A1
+8 more (S120P) | Single nucleotide variant (missense variant +1 more) | Crigler-Najjar syndrome, type II +1 more | |
| | UGT1A10, UGT1A
+8 more (L140fs) | Deletion (frameshift variant +1 more) | Crigler-Najjar syndrome, type II | |
| | UGT1A, UGT1A1
+8 more (Y486D +4 more) | Single nucleotide variant (missense variant) | Crigler-Najjar syndrome, type II +7 more | GPathogenic/Likely pathogenic |
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