| | | Deletion (frameshift variant +1 more) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (splice donor variant) | Familial adenomatous polyposis 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary cancer-predisposing syndrome +8 more | |
| | | Indel (intron variant) | Familial adenomatous polyposis 1 | |
| | | Duplication (frameshift variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (nonsense) | Familial adenomatous polyposis 1 | |
| | | Duplication (frameshift variant) | Familial adenomatous polyposis 1 | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (nonsense) | Familial adenomatous polyposis 1 | |
| | | Deletion (nonsense) | Familial adenomatous polyposis 1 | |
| | | Deletion (nonsense) | Familial adenomatous polyposis 1 | |
| | | Deletion (frameshift variant +1 more) | Familial multiple polyposis syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | Colorectal cancer, susceptibility to +7 more | GConflicting classifications of pathogenicity; association; risk factor |
| | | Microsatellite (frameshift variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (nonsense) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (nonsense) | Familial adenomatous polyposis 1 +1 more | |
| | | Deletion (frameshift variant) | Familial adenomatous polyposis 1 +2 more | |