Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001503924 | SCV001708785 | likely benign | ALG2-congenital disorder of glycosylation; Congenital myasthenic syndrome 14 | 2024-01-15 | criteria provided, single submitter | clinical testing |