Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000803084 | SCV000942943 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2022-09-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002495085 | SCV002782587 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2022-05-03 | criteria provided, single submitter | clinical testing |