Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000635031 | SCV000756409 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2022-03-19 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002483798 | SCV002780284 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-08-09 | criteria provided, single submitter | clinical testing |