Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000951526 | SCV001097931 | likely benign | not provided | 2018-03-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002488033 | SCV002803295 | likely benign | Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema | 2021-09-25 | criteria provided, single submitter | clinical testing |