Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001510492 | SCV001717537 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2020-08-15 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002497100 | SCV002794754 | likely benign | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2022-02-02 | criteria provided, single submitter | clinical testing |