Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001724740 | SCV001949999 | uncertain significance | Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold | 2021-07-28 | criteria provided, single submitter | clinical testing |