Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001439834 | SCV001642731 | likely benign | Hereditary spastic paraplegia 7 | 2020-01-24 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000465167 | SCV001756025 | likely benign | not provided | 2020-03-02 | criteria provided, single submitter | clinical testing |