Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000578420 | SCV000680428 | pathogenic | Intellectual disability, X-linked 99, syndromic, female-restricted | 2017-11-16 | criteria provided, single submitter | clinical testing |