Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Diagnostics Laboratory, |
RCV000761322 | SCV000891307 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 22 | 2017-04-11 | criteria provided, single submitter | clinical testing |