Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV001004076 | SCV001162800 | pathogenic | Autosomal recessive Alport syndrome | 2017-09-11 | criteria provided, single submitter | clinical testing |