Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000557765 | SCV000637901 | likely benign | Hereditary Paraganglioma-Pheochromocytoma Syndromes | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000574509 | SCV000675046 | likely benign | Hereditary cancer-predisposing syndrome | 2017-06-15 | criteria provided, single submitter | clinical testing | Synonymous alterations with insufficient evidence to classify as benign |