Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000995514 | SCV001149717 | pathogenic | Autosomal recessive Alport syndrome | 2018-03-16 | criteria provided, single submitter | clinical testing |