| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RAD51D, RAD51L3-RFFL (R253* +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (C9fs) | Deletion (frameshift variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 | |
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