Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002198291 | SCV002487094 | likely benign | DPAGT1-congenital disorder of glycosylation; Congenital myasthenic syndrome 13 | 2022-03-18 | criteria provided, single submitter | clinical testing |