Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000625586 | SCV001149729 | pathogenic | X-linked Alport syndrome | 2019-06-13 | criteria provided, single submitter | clinical testing | |
Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV000625586 | SCV000746085 | pathogenic | X-linked Alport syndrome | 2017-09-18 | no assertion criteria provided | clinical testing |