Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001484018 | SCV001688426 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2020-02-05 | criteria provided, single submitter | clinical testing |