Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001788934 | SCV002030031 | benign | Congenital disorder of glycosylation, type IAA | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001788935 | SCV002030032 | benign | Intellectual disability, autosomal dominant 55, with seizures | 2021-09-05 | criteria provided, single submitter | clinical testing |