| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | VRK2, FANCL (T372fs +3 more) | Duplication (frameshift variant +1 more) | FANCL-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Fanconi anemia complementation group L +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene