Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000671364 | SCV000796332 | likely benign | Very long chain acyl-CoA dehydrogenase deficiency | 2017-12-15 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001797123 | SCV002038932 | likely benign | not provided | 2021-06-14 | criteria provided, single submitter | clinical testing |