Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003809164 | SCV004596630 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2023-12-28 | criteria provided, single submitter | clinical testing |