| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | UGT1A, UGT1A10 +5 more (A232fs) | Deletion (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | UGT1A, UGT1A10 +6 more (E50D) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | Lucey-Driscoll syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity; drug response; other |
| | | Single nucleotide variant (synonymous variant +1 more) | UGT1A1-related condition +6 more | GConflicting classifications of pathogenicity |
| | UGT1A3, UGT1A4 +8 more (V59F) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | UGT1A, UGT1A1 +8 more (G71R) | Single nucleotide variant (missense variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity; drug response |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | UGT1A1, UGT1A10 +8 more (V231M +4 more) | Single nucleotide variant (missense variant) | not provided | |
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