Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Statistical Genetics, |
RCV000226627 | SCV000282037 | pathogenic | Autosomal recessive nonsyndromic hearing loss 3 | 2016-06-06 | no assertion criteria provided | research |