Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000810742 | SCV000950975 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2022-09-06 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002507411 | SCV002814747 | uncertain significance | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2022-04-12 | criteria provided, single submitter | clinical testing |