Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
National Institute on Deafness and Communication Disorders, |
RCV000417169 | SCV000494730 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 3 | 2016-03-01 | no assertion criteria provided | research |