Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000623212 | SCV000741255 | likely pathogenic | Inborn genetic diseases | 2016-01-15 | criteria provided, single submitter | clinical testing | |
Vavilov Institute of General Genetics RAS, |
RCV000190539 | SCV000221289 | pathogenic | Spinocerebellar ataxia, X-linked | no assertion criteria provided | case-control |