Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001486092 | SCV001690542 | likely benign | Very long chain acyl-CoA dehydrogenase deficiency | 2023-12-09 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004704613 | SCV005218615 | likely benign | not provided | criteria provided, single submitter | not provided |