Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Medical Genetics and Applied Genomics, |
RCV001693506 | SCV001911528 | uncertain significance | Autosomal dominant nonsyndromic hearing loss; Autosomal dominant nonsyndromic hearing loss 64 | 2021-09-16 | criteria provided, single submitter | clinical testing |