Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000474580 | SCV000554473 | likely benign | Hereditary Paraganglioma-Pheochromocytoma Syndromes | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000568431 | SCV000673598 | likely benign | Hereditary cancer-predisposing syndrome | 2015-11-03 | criteria provided, single submitter | clinical testing | Synonymous alterations with insufficient evidence to classify as benign |