Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001890484 | SCV002151020 | likely benign | Joubert syndrome 23; Short-rib thoracic dysplasia 14 with polydactyly | 2023-11-27 | criteria provided, single submitter | clinical testing |