Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV000984598 | SCV001132656 | uncertain significance | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | 2019-05-24 | no assertion criteria provided | clinical testing |