Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000907757 | SCV001052482 | likely benign | not provided | 2018-03-29 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002479043 | SCV002795814 | likely benign | Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema | 2022-04-21 | criteria provided, single submitter | clinical testing |