Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Biochemical Molecular Genetic Laboratory, |
RCV001283801 | SCV001469191 | likely pathogenic | X-linked intellectual disability-cerebellar hypoplasia syndrome | 2020-09-10 | no assertion criteria provided | clinical testing |