Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000130761 | SCV000185653 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-01-30 | criteria provided, single submitter | clinical testing | Lines of evidence used in support of classification: Co-occurence with a mutation in another gene that clearly explains a proband's phenotype,Insufficient evidence |