Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000646026 | SCV000767782 | benign | Familial acute necrotizing encephalopathy | 2023-08-28 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004708974 | SCV005246517 | benign | not provided | criteria provided, single submitter | not provided |