Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Myriad Genetics, |
RCV001263569 | SCV001441660 | likely pathogenic | GNE myopathy | 2019-12-28 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV001263569 | SCV004191660 | likely pathogenic | GNE myopathy | 2023-03-06 | criteria provided, single submitter | clinical testing |