Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000550688 | SCV000632135 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2024-01-27 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002506313 | SCV002802533 | likely benign | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2022-03-17 | criteria provided, single submitter | clinical testing |