Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000995739 | SCV001150067 | pathogenic | X-linked Alport syndrome | 2018-12-11 | criteria provided, single submitter | clinical testing | |
Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV000995739 | SCV001192609 | pathogenic | X-linked Alport syndrome | 2019-08-09 | no assertion criteria provided | clinical testing |