Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002167964 | SCV002348975 | likely benign | not provided | 2022-11-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002498145 | SCV002812532 | likely benign | Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema | 2022-01-18 | criteria provided, single submitter | clinical testing |