Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000703008 | SCV000831887 | likely benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2022-12-02 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002507230 | SCV002814523 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-08-25 | criteria provided, single submitter | clinical testing |