Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Athena Diagnostics Inc | RCV000993337 | SCV001146206 | benign | not provided | 2019-04-19 | criteria provided, single submitter | clinical testing | |
Institute of Human Genetics, |
RCV001253304 | SCV001428954 | uncertain significance | Autosomal dominant nonsyndromic hearing loss 56 | 2016-10-19 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000993337 | SCV002004493 | likely benign | not provided | 2020-03-24 | criteria provided, single submitter | clinical testing |