Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001718922 | SCV000721403 | likely benign | not provided | 2021-01-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001496412 | SCV001701111 | likely benign | Combined oxidative phosphorylation defect type 27 | 2022-12-29 | criteria provided, single submitter | clinical testing |