| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FANCD2, LOC107303338 (R119H) | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi anemia +4 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi anemia complementation group D2 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Fanconi anemia complementation group D2 +1 more | |
| | FANCD2, LOC107303338 (L456R) | Single nucleotide variant (missense variant) | Hereditary breast ovarian cancer syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | FANCD2, LOC107303338 (Q623P +1 more) | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (intron variant) | Fanconi anemia complementation group D2 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | FANCD2, LOC107303338 (P714L +1 more) | Single nucleotide variant (missense variant) | Hereditary breast ovarian cancer syndrome +5 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary breast ovarian cancer syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Fanconi anemia +4 more | |
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