Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002104309 | SCV002432669 | likely benign | not provided | 2023-12-14 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002500152 | SCV002805934 | likely benign | Epilepsy, idiopathic generalized, susceptibility to, 11; Familial hyperaldosteronism type II; Leukoencephalopathy with mild cerebellar ataxia and white matter edema | 2021-09-05 | criteria provided, single submitter | clinical testing |