| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | SUFU-related disorder +5 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial meningioma +4 more | |
| | | Single nucleotide variant (missense variant) | Familial meningioma +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial meningioma +5 more | GConflicting classifications of pathogenicity |
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