| | | Deletion (frameshift variant +2 more) | Fanconi anemia complementation group D1 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary breast ovarian cancer syndrome | |
| | | Deletion (intron variant) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary breast ovarian cancer syndrome | |
| | | Insertion (non-coding transcript variant +1 more) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (splice donor variant) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary breast ovarian cancer syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Malignant tumor of breast | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Deletion (inframe_indel +2 more) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Deletion (frameshift variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (nonsense +2 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Duplication (frameshift variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (nonsense +1 more) | Familial cancer of breast | |
| | | Duplication (frameshift variant +2 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Duplication (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Familial cancer of breast | |
| | | Insertion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (splice acceptor variant) | Familial cancer of breast | |
| | | Deletion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Insertion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Insertion | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (nonsense +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Duplication (nonsense +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +1 more) | Familial cancer of breast | |
| | | Duplication (frameshift variant +2 more) | Familial cancer of breast | |
| | | Indel (frameshift variant +1 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Deletion (frameshift variant +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Deletion (nonsense +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Familial cancer of breast | |
| | | Deletion (inframe deletion +2 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Duplication (frameshift variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | Familial cancer of breast | |
| | | Indel (frameshift variant +3 more) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Deletion (frameshift variant +2 more) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Single nucleotide variant (missense variant +2 more) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Insertion (inframe_insertion +1 more) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Deletion (frameshift variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (missense variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Deletion (frameshift variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Deletion (frameshift variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Duplication (inframe_insertion +1 more) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Duplication (frameshift variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Deletion (frameshift variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (intron variant) | Breast-ovarian cancer, familial, susceptibility to, 2 | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 2 | |