Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Biesecker Lab/Clinical Genomics Section, |
RCV000211600 | SCV000268683 | likely benign | Autosomal dominant nonsyndromic hearing loss 48 | 2016-05-10 | no assertion criteria provided | research |