Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center For Human Genetics And Laboratory Diagnostics, |
RCV000678986 | SCV000805202 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 12 | 2018-04-25 | criteria provided, single submitter | clinical testing |