Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Biochemical Molecular Genetic Laboratory, |
RCV000723311 | SCV000854702 | likely pathogenic | Syndromic X-linked intellectual disability Najm type | 2018-06-04 | no assertion criteria provided | clinical testing |