Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Revvity Omics, |
RCV001175218 | SCV003811243 | likely pathogenic | Joubert syndrome 22 | 2022-04-05 | criteria provided, single submitter | clinical testing | |
Department Of Translational Genomics |
RCV001175218 | SCV001338742 | likely pathogenic | Joubert syndrome 22 | no assertion criteria provided | research |