Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000988572 | SCV000259317 | likely benign | Multiple endocrine neoplasia, type 1 | 2019-12-31 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV000506264 | SCV000604205 | likely benign | not specified | 2016-09-12 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000574517 | SCV000664496 | likely benign | Hereditary cancer-predisposing syndrome | 2015-12-04 | criteria provided, single submitter | clinical testing | Synonymous alterations with insufficient evidence to classify as benign |
Mendelics | RCV000988572 | SCV001138342 | likely benign | Multiple endocrine neoplasia, type 1 | 2019-05-28 | criteria provided, single submitter | clinical testing |