Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Testing Center for Deafness, |
RCV000770814 | SCV000902300 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 12 | 2019-02-26 | no assertion criteria provided | case-control |