Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Testing Center for Deafness, |
RCV000770815 | SCV000902302 | likely pathogenic | Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 | 2019-02-26 | no assertion criteria provided | case-control |