Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001483321 | SCV001687710 | likely benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2019-08-07 | criteria provided, single submitter | clinical testing |