Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
The Shared Resource Centre "Genome", |
RCV002444385 | SCV002754445 | likely pathogenic | Usher syndrome type 2A | 2022-11-10 | criteria provided, single submitter | clinical testing |