Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV000501656 | SCV000596755 | likely benign | not specified | 2017-02-28 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002060142 | SCV002491388 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2023-05-25 | criteria provided, single submitter | clinical testing |