| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RAD51D, RAD51L3-RFFL (S207L +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Breast and/or ovarian cancer +4 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (S207P +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 +2 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (A190D +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 | |
| | RAD51D, RAD51L3-RFFL (E184K +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | RAD51L3-RFFL, RAD51D (R55W) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
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