| | | Single nucleotide variant (nonsense) | PALB2-related disorder +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +8 more | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Deletion (frameshift variant) | not provided +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +3 more | |
| | | Single nucleotide variant (nonsense) | Familial cancer of breast +2 more | |
| | | Deletion (frameshift variant) | not provided +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (splice donor variant +1 more) | Familial cancer of breast +2 more | |
| | | Single nucleotide variant (nonsense) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Duplication (frameshift variant) | Breast and/or ovarian cancer +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Fanconi anemia complementation group N +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial cancer of breast +6 more | |
| | | Single nucleotide variant (nonsense) | Hereditary breast ovarian cancer syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | PALB2-related disorder +7 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Neoplasm of ovary +1 more | |
| | | Microsatellite (frameshift variant) | Familial cancer of breast +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Microsatellite (frameshift variant) | Pancreatic cancer, susceptibility to, 3 +4 more | |
| | | Deletion (frameshift variant) | Colorectal cancer +4 more | |