Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001004819 | SCV001164312 | uncertain significance | Anophthalmia; Renal agenesis | 2019-07-10 | no assertion criteria provided | clinical testing |