Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002106078 | SCV002435688 | likely benign | Myasthenic syndrome, congenital, 22 | 2023-11-14 | criteria provided, single submitter | clinical testing |