| | | Single nucleotide variant (intron variant) | not specified | |
| | BRCA1, LOC126862571 (R1347G +21 more) | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (S1321C +21 more) | Single nucleotide variant (missense variant +1 more) | Hereditary breast ovarian cancer syndrome +2 more | GConflicting classifications of pathogenicity |
| | BRCA1, LOC126862571 (I1275V +21 more) | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (L1261F +21 more) | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | BRCA1, LOC126862571 (P1238L +21 more) | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (K1183R +21 more) | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |
| | BRCA1, LOC126862571 (S1140G +21 more) | Single nucleotide variant (missense variant +1 more) | BRCA1-related cancer predisposition | |
| | BRCA1, LOC126862571 (P1099L +20 more) | Single nucleotide variant (missense variant +1 more) | Breast-ovarian cancer, familial, susceptibility to, 1 | |