| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130004614, SUFU (P24fs) | Deletion (frameshift variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Gorlin syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +5 more | |
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