Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002120934 | SCV002440260 | likely benign | Peroxisome biogenesis disorder 2B | 2025-01-23 | criteria provided, single submitter | clinical testing |