Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001253448 | SCV001429156 | likely pathogenic | Nicolaides-Baraitser syndrome | 2016-06-24 | criteria provided, single submitter | clinical testing | This variant was identified as de novo (maternity and paternity confirmed). |