Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Myriad Genetics, |
RCV003452251 | SCV004186154 | pathogenic | Familial cancer of breast | 2023-09-12 | criteria provided, single submitter | clinical testing | This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation. |
Baylor Genetics | RCV003452251 | SCV004202764 | likely pathogenic | Familial cancer of breast | 2022-01-01 | criteria provided, single submitter | clinical testing |