Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000210664 | SCV000262845 | pathogenic | Inborn genetic diseases | 2013-10-24 | criteria provided, single submitter | clinical testing | |
Molecular Diagnostics Lab, |
RCV003237344 | SCV003936048 | pathogenic | Microcephalic osteodysplastic primordial dwarfism type II | 2020-05-05 | criteria provided, single submitter | clinical testing |