Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000951619 | SCV001098032 | likely benign | Joubert syndrome 23; Short-rib thoracic dysplasia 14 with polydactyly | 2023-12-11 | criteria provided, single submitter | clinical testing |