Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000165521 | SCV000216253 | uncertain significance | Hereditary cancer-predisposing syndrome | 2014-08-12 | criteria provided, single submitter | clinical testing | Lines of evidence used in support of classification: Detected in individual satisfying established diagnostic critera for classic disease without a clear mutation,Insufficient or conflicting evidence |