Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002073846 | SCV002371877 | benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2024-01-25 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002494149 | SCV002796796 | likely benign | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2021-10-14 | criteria provided, single submitter | clinical testing |