Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001253092 | SCV001428621 | likely pathogenic | Hearing loss, X-linked 4 | 2017-10-04 | criteria provided, single submitter | clinical testing |