Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
EGL Genetic Diagnostics, |
RCV000592715 | SCV000707711 | uncertain significance | not provided | 2017-05-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000653043 | SCV000774917 | likely benign | Norman-Roberts syndrome; Epilepsy, familial temporal lobe, 7 | 2019-12-31 | criteria provided, single submitter | clinical testing |