Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Genetics Laboratory, |
RCV000505245 | SCV000599237 | likely pathogenic | ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder | 2016-04-22 | no assertion criteria provided | clinical testing |