Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000995818 | SCV001150182 | pathogenic | Nephrotic syndrome, type 2 | 2019-05-08 | criteria provided, single submitter | clinical testing |