Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001506756 | SCV001711690 | likely benign | Nemaline myopathy 2 | 2022-10-27 | criteria provided, single submitter | clinical testing |