Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000692930 | SCV000820781 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2023-07-16 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002499238 | SCV002775795 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-10-20 | criteria provided, single submitter | clinical testing |