Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center For Human Genetics And Laboratory Diagnostics, |
RCV000678966 | SCV000805182 | pathogenic | X-linked Alport syndrome | 2018-05-22 | criteria provided, single submitter | clinical testing |