Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001037908 | SCV001201344 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2023-10-03 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002505559 | SCV002816540 | uncertain significance | Epilepsy, familial temporal lobe, 1; Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2021-10-25 | criteria provided, single submitter | clinical testing |