Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000461014 | SCV000562731 | likely benign | Hereditary Paraganglioma-Pheochromocytoma Syndromes | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001014772 | SCV001175526 | likely benign | Hereditary cancer-predisposing syndrome | 2018-05-09 | criteria provided, single submitter | clinical testing | Synonymous alterations with insufficient evidence to classify as benign |