Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000534570 | SCV000632197 | likely benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2023-08-05 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002497096 | SCV002813072 | likely benign | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2022-04-20 | criteria provided, single submitter | clinical testing |