Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV000415302 | SCV000492909 | likely pathogenic | Sensorineural hearing loss disorder | 2015-03-17 | criteria provided, single submitter | clinical testing |