Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000571861 | SCV000672673 | uncertain significance | Hereditary cancer-predisposing syndrome | 2016-08-30 | criteria provided, single submitter | clinical testing | Lines of evidence used in support of classification: Insufficient evidence,In silico models in agreement (benign) |