| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Duplication (frameshift variant) | Fanconi anemia complementation group C +3 more | |
| | | Single nucleotide variant (missense variant) | Fanconi anemia | |
Click to view in NCBI Gene