Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Evidence- |
RCV000111863 | SCV000299768 | pathogenic | Breast-ovarian cancer, familial, susceptibility to, 1 | 2016-09-08 | reviewed by expert panel | curation | Variant allele predicted to encode a truncated non-functional protein. |
Department of Medical Genetics, |
RCV000111863 | SCV000564300 | pathogenic | Breast-ovarian cancer, familial, susceptibility to, 1 | 2015-07-01 | criteria provided, single submitter | clinical testing | |
Breast Cancer Information Core |
RCV000111863 | SCV000144437 | pathogenic | Breast-ovarian cancer, familial, susceptibility to, 1 | 2003-01-22 | no assertion criteria provided | clinical testing |