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Variants called in agreement with Myriad results
| Variants | Clinical significance | Number of samples |
|---|---|---|
| BRCA1 c.5266dupC | Pathogenic | 2 |
| BRAC1 c.5095C>T | Pathogenic | 1 |
| BRCA1 c.3916_3917del | Pathogenic | 1 |
| BRCA2 c.6988A>G | VUS | 1 |
| BRCA2 c.8482A>G | VUS | 1 |
| BRCA2 c.8518A>G | VUS | 1 |
