Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000573651 | SCV000662407 | likely benign | Hereditary cancer-predisposing syndrome | 2017-08-04 | criteria provided, single submitter | clinical testing | Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign |
Color | RCV000573651 | SCV000690214 | likely benign | Hereditary cancer-predisposing syndrome | 2016-03-02 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV000679217 | SCV000805848 | likely benign | not provided | 2017-09-22 | criteria provided, single submitter | clinical testing |