Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001262536 | SCV001440453 | likely benign | Intellectual disability, X-linked syndromic, Turner type | 2019-01-01 | criteria provided, single submitter | clinical testing |