Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Biochemical Molecular Genetic Laboratory, |
RCV000985163 | SCV001133164 | likely pathogenic | ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder | 2019-09-26 | no assertion criteria provided | clinical testing |