Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Diagnostics Laboratory, |
RCV000761233 | SCV000891189 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 36 | 2018-09-19 | criteria provided, single submitter | clinical testing |