Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Department of Genetics, |
RCV001264731 | SCV001442962 | likely pathogenic | Intellectual disability-severe speech delay-mild dysmorphism syndrome | 2020-04-03 | no assertion criteria provided | clinical testing |