Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000873658 | SCV001015691 | likely benign | Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 | 2024-01-06 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001593096 | SCV001816236 | likely benign | not provided | 2021-04-26 | criteria provided, single submitter | clinical testing |