Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001575513 | SCV001802525 | uncertain significance | not provided | 2023-09-20 | criteria provided, single submitter | clinical testing | In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge |
Labcorp Genetics |
RCV001575513 | SCV002213868 | likely benign | not provided | 2023-05-22 | criteria provided, single submitter | clinical testing |