Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000812866 | SCV000953196 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2022-12-06 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002501111 | SCV002775673 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-09-03 | criteria provided, single submitter | clinical testing |