Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center For Human Genetics And Laboratory Diagnostics, |
RCV001353238 | SCV001548381 | uncertain significance | Autosomal dominant Alport syndrome | 2021-03-03 | criteria provided, single submitter | clinical testing |