| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (3 prime UTR variant +2 more) | Fanconi anemia +3 more | GPathogenic/Likely pathogenic |
| | FANCA, LOC130059837
+1 more | Copy number loss | Fanconi anemia complementation group A | |
| | | Deletion (frameshift variant) | Fanconi anemia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
Click to view in NCBI Gene