Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Evidence- |
RCV000239064 | SCV000783152 | pathogenic | Breast-ovarian cancer, familial, susceptibility to, 1 | 2017-12-15 | reviewed by expert panel | curation | Variant allele predicted to encode a truncated non-functional protein. |
Sharing Clinical Reports Project |
RCV000239064 | SCV000297485 | pathogenic | Breast-ovarian cancer, familial, susceptibility to, 1 | 2013-12-17 | no assertion criteria provided | clinical testing |