Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV001254145 | SCV001430094 | likely pathogenic | Autosomal recessive Alport syndrome | 2020-04-20 | criteria provided, single submitter | clinical testing |