| | | Indel (nonsense +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | LOC126862571, BRCA1 (Q1312fs +21 more) | Deletion (frameshift variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 +1 more | |
| | | Deletion (nonsense +2 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (L1193fs +21 more) | Indel (frameshift variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (T1088fs +21 more) | Deletion (frameshift variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | | Deletion (frameshift variant +2 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (F1146fs +21 more) | Deletion (frameshift variant +1 more) | Hereditary breast ovarian cancer syndrome +1 more | |
| | BRCA1, LOC126862571 (P1190L +21 more) | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | BRCA1, LOC126862571 (E1172G +21 more) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | BRCA1, LOC126862571 (M1137T +21 more) | Single nucleotide variant (intron variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | BRCA1, LOC126862571 (P1126L +20 more) | Single nucleotide variant (intron variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | BRCA1, LOC126862571 (V1120D +20 more) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |