Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001042042 | SCV001205700 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2022-09-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002489575 | SCV002775965 | uncertain significance | Epilepsy, familial temporal lobe, 1; Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2022-05-19 | criteria provided, single submitter | clinical testing |