Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002077947 | SCV002324213 | benign | Brachyolmia-amelogenesis imperfecta syndrome | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004718990 | SCV005318457 | benign | not provided | criteria provided, single submitter | not provided |