| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial adenomatous polyposis 2 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial adenomatous polyposis 2 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Diffuse midline glioma, H3 K27-altered +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +5 more | |
| | | Single nucleotide variant (nonsense +2 more) | Familial adenomatous polyposis 2 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +14 more | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +14 more | |
| | | Single nucleotide variant (missense variant) | Cowden syndrome +17 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | APC-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Familial adenomatous polyposis 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +4 more) | not provided +5 more | |
| | | Single nucleotide variant (nonsense +2 more) | Familial multiple polyposis syndrome +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Familial adenomatous polyposis 1 +7 more | |
| | | Single nucleotide variant (nonsense +2 more) | Familial multiple polyposis syndrome +8 more | |
| | | Single nucleotide variant (nonsense +2 more) | Desmoid disease, hereditary +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial adenomatous polyposis 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (splice donor variant) | Desmoid disease, hereditary +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Familial multiple polyposis syndrome +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Familial multiple polyposis syndrome +8 more | |
| | | Single nucleotide variant (nonsense) | Familial adenomatous polyposis 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | APC-Associated Polyposis Disorders +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hepatocellular carcinoma +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Desmoid disease, hereditary +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +7 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Acrocephalosyndactyly type I +11 more | |
| | | Single nucleotide variant (missense variant +2 more) | Beare-Stevenson cutis gyrata syndrome +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +2 more) | FGFR2-related craniosynostosis +15 more | |
| | | Single nucleotide variant (missense variant +2 more) | FGFR2-related craniosynostosis +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Crouzon syndrome +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | not provided +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not provided +13 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Bent bone dysplasia syndrome 1 +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome | |