Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
University of Washington Department of Laboratory Medicine, |
RCV003157411 | SCV003851049 | likely benign | Hereditary cancer-predisposing syndrome | 2023-03-23 | criteria provided, single submitter | curation | Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673). |
Pathway Genomics | RCV000144579 | SCV000189886 | uncertain significance | Breast-ovarian cancer, familial, susceptibility to, 1 | 2014-07-24 | no assertion criteria provided | clinical testing |