Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000819828 | SCV000960510 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2023-11-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002478916 | SCV002792203 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-07-21 | criteria provided, single submitter | clinical testing |