Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002542243 | SCV001076740 | likely benign | Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV | 2022-08-21 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002502843 | SCV002804674 | likely benign | Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV | 2022-05-03 | criteria provided, single submitter | clinical testing |