Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000623747 | SCV000741207 | likely pathogenic | Inborn genetic diseases | 2015-11-16 | criteria provided, single submitter | clinical testing | |
Ce |
RCV002263835 | SCV002544374 | likely pathogenic | not provided | 2022-04-01 | criteria provided, single submitter | clinical testing |