Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001421553 | SCV001624079 | likely benign | Neuropathy, hereditary sensory and autonomic, type 2A; Generalized epilepsy with febrile seizures plus, type 7 | 2023-08-17 | criteria provided, single submitter | clinical testing | |
New York Genome Center | RCV001839043 | SCV002099020 | uncertain significance | Seizure | 2021-02-24 | criteria provided, single submitter | clinical testing |