Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000190722 | SCV000244163 | uncertain significance | Inborn genetic diseases | 2014-11-13 | criteria provided, single submitter | clinical testing | |
Daan van Aalten Lab, |
RCV000991240 | SCV001142636 | pathogenic | Intellectual disability, X-linked 106 | no assertion criteria provided | literature only | ||
OMIM | RCV000991240 | SCV002576384 | pathogenic | Intellectual disability, X-linked 106 | 2022-09-25 | no assertion criteria provided | literature only |