| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Fanconi anemia, complementation group W +1 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi anemia, complementation group W +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Fanconi anemia, complementation group W +1 more | |
Click to view in NCBI Gene