Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000806109 | SCV000946091 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2024-01-07 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002507395 | SCV002815542 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-11-29 | criteria provided, single submitter | clinical testing |