Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000541980 | SCV000625298 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000563213 | SCV000662322 | likely benign | Hereditary cancer-predisposing syndrome | 2016-11-25 | criteria provided, single submitter | clinical testing | Synonymous alterations with insufficient evidence to classify as benign |
Color | RCV000563213 | SCV000912997 | likely benign | Hereditary cancer-predisposing syndrome | 2018-10-19 | criteria provided, single submitter | clinical testing |