Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001471925 | SCV001676048 | likely benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2023-09-28 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002503003 | SCV002811432 | likely benign | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-10-15 | criteria provided, single submitter | clinical testing |