| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | LOC132090450, FANCA (T1131A) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group A +2 more | GPathogenic/Likely pathogenic |
| | FANCA, LOC132090450 (D1129H) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group A +2 more | |
| | FANCA, LOC132090450 (Q1128E) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group A +1 more | |
| | FANCA, LOC132090450 (A1125T) | Single nucleotide variant (missense variant) | Fanconi anemia +1 more | |
Click to view in NCBI Gene