Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory of Prof. |
RCV000225012 | SCV000281992 | pathogenic | Autosomal recessive nonsyndromic hearing loss 77 | 2016-02-16 | no assertion criteria provided | research | Congenital, profound HL |