Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV001267041 | SCV001445222 | uncertain significance | Inborn genetic diseases | 2019-04-29 | criteria provided, single submitter | clinical testing | |
University of Washington Center for Mendelian Genomics, |
RCV001257970 | SCV001434783 | uncertain significance | Cleft lip/palate | no assertion criteria provided | research |