Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000838622 | SCV000980496 | likely benign | not provided | 2020-01-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001080573 | SCV001092407 | likely benign | Combined oxidative phosphorylation defect type 27 | 2023-12-30 | criteria provided, single submitter | clinical testing |