Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002176220 | SCV002471545 | likely benign | Cone-rod dystrophy 6; Leber congenital amaurosis 1 | 2023-12-28 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004703247 | SCV005218698 | likely benign | not provided | criteria provided, single submitter | not provided |