| | | Single nucleotide variant (splice donor variant) | Colon cancer | |
| | | Deletion (frameshift variant) | Colon cancer | |
| | | Deletion | Colon cancer | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Deletion (frameshift variant +2 more) | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication (frameshift variant +2 more) | Colon cancer | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Familial adenomatous polyposis 1 | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (splice donor variant) | Colorectal cancer, hereditary nonpolyposis, type 2 +3 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | not provided | Gno classifications from unflagged records |
| | | Microsatellite (frameshift variant) | Colorectal cancer, hereditary nonpolyposis, type 2 +1 more | |
| | | Deletion (inframe_deletion) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial adenomatous polyposis 1 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | POLD1-related condition +5 more | |
| | | Single nucleotide variant (missense variant) | Polycystic kidney disease 4 +2 more | |
| | | Single nucleotide variant (intron variant) | MUTYH-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | CHEK2-related condition +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fanconi anemia complementation group U +4 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | CDH1-related diffuse gastric and lobular breast cancer syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | MUTYH-related condition +8 more | GPathogenic/Likely pathogenic |