Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Molecular Medicine, |
RCV001078192 | SCV000998850 | pathogenic | Hypoparathyroidism, deafness, renal disease syndrome | 2019-10-23 | no assertion criteria provided | clinical testing |