| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Familial adenomatous polyposis 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Familial multiple polyposis syndrome +6 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) | Familial adenomatous polyposis 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Deletion (frameshift variant +1 more) | Familial multiple polyposis syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity; association; risk factor |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Classic or attenuated familial adenomatous polyposis +4 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +5 more | |
| | | Single nucleotide variant (missense variant) | Diffuse midline glioma, H3 K27-altered +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +3 more | |
| | | Single nucleotide variant (missense variant) | APC-Associated Polyposis Disorders +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |