| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FANCF, LOC130005443 (Q363*) | Single nucleotide variant (nonsense) | Fanconi anemia +3 more | |
| | FANCF, LOC130005443 (R355C) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group F | |
| | FANCF, LOC130005443 (T331I) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | FANCF, LOC130005443 (P318S) | Single nucleotide variant (missense variant) | Fanconi anemia +1 more | |
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