Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV003466671 | SCV004212208 | likely pathogenic | Familial cancer of breast | 2022-09-27 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV003466671 | SCV004931718 | pathogenic | Familial cancer of breast | 2024-01-24 | criteria provided, single submitter | clinical testing | This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation. |