Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001486192 | SCV001690646 | likely benign | Combined oxidative phosphorylation defect type 27 | 2023-12-30 | criteria provided, single submitter | clinical testing |