Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001253221 | SCV001428830 | likely pathogenic | Intellectual disability, autosomal dominant 20 | 2018-12-20 | criteria provided, single submitter | clinical testing |