Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001262396 | SCV001440244 | likely pathogenic | Syndromic X-linked intellectual disability Claes-Jensen type | 2019-01-01 | criteria provided, single submitter | clinical testing |