| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Breast-ovarian cancer, familial, susceptibility to, 4 | |
| | RAD51D, RAD51L3-RFFL (S207L +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary breast ovarian cancer syndrome +4 more | GConflicting classifications of pathogenicity |
| | RAD51L3-RFFL, RAD51D (S207P +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary cancer-predisposing syndrome +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 | |
| | RAD51L3-RFFL, RAD51D (E184K +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 +3 more | |
| | RAD51L3-RFFL, RAD51D (N138D +1 more) | Single nucleotide variant (missense variant +2 more) | not specified +3 more | |
| | RAD51D, RAD51L3-RFFL (R108C) | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 4 +1 more | GConflicting classifications of pathogenicity |
| | RAD51D, RAD51L3-RFFL (R55W) | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
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