Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002165286 | SCV002339915 | likely benign | Peroxisome biogenesis disorder 2B | 2022-11-03 | criteria provided, single submitter | clinical testing |