Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV001029938 | SCV001192734 | likely pathogenic | Autosomal dominant Alport syndrome | 2019-11-24 | no assertion criteria provided | clinical testing |