Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001403816 | SCV001605701 | likely benign | Cone-rod dystrophy 6; Leber congenital amaurosis 1 | 2023-12-13 | criteria provided, single submitter | clinical testing | |
Institute of Human Genetics, |
RCV004815529 | SCV005072136 | uncertain significance | Retinal dystrophy | 2012-01-01 | no assertion criteria provided | clinical testing |