Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV001816377 | SCV002062527 | likely benign | not provided | 2022-11-01 | criteria provided, single submitter | clinical testing | CLCN2: BP4, BP7 |
Labcorp Genetics |
RCV001816377 | SCV002402030 | likely benign | not provided | 2023-06-29 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002482349 | SCV002798624 | likely benign | Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema | 2021-11-13 | criteria provided, single submitter | clinical testing |