Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Myriad Genetics, |
RCV003454093 | SCV004189479 | pathogenic | Familial cancer of breast | 2023-09-06 | criteria provided, single submitter | clinical testing | This variant is considered pathogenic. This variant creates a termination codon and is predicted to result in premature protein truncation. |
BRCAlab, |
RCV003156022 | SCV002588983 | pathogenic | Hereditary breast ovarian cancer syndrome | 2022-08-26 | no assertion criteria provided | clinical testing |