| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, susceptibility to, 10 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | Colorectal cancer, susceptibility to, 10 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Colorectal cancer, susceptibility to, 10 +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene