| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (5 prime UTR variant) | Fanconi anemia complementation group E | |
| | | Single nucleotide variant (missense variant) | Fanconi anemia complementation group E | |
| | FANCE, LOC129996245 (A11T) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group E | |
| | FANCE, LOC129996245 (P18S) | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | FANCE, LOC129996245 (R41W) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group E | |
| | LOC129996245, FANCE (R69Q) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group E +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Fanconi anemia complementation group E | GConflicting classifications of pathogenicity |
| | FANCE, LOC129996245 (P77T) | Single nucleotide variant (missense variant) | FANCE-related condition +4 more | |
| | | Single nucleotide variant (intron variant) | Fanconi anemia +2 more | |