Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Molecular Medicine, |
RCV001293015 | SCV001481784 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 102 | 2021-08-16 | criteria provided, single submitter | clinical testing |