Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Evidence- |
RCV000495425 | SCV000578136 | likely benign | Breast-ovarian cancer, familial, susceptibility to, 1 | 2017-06-29 | reviewed by expert panel | curation | Synonymous substitution variant, with low bioinformatic likelihood to result in a splicing aberration (Splicing prior probability 0.02; http://priors.hci.utah.edu/PRIORS/). |
Invitae | RCV001434547 | SCV001637357 | likely benign | Hereditary breast ovarian cancer syndrome | 2021-08-20 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001524383 | SCV001734209 | likely benign | Hereditary cancer-predisposing syndrome | 2021-01-05 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000921915 | SCV001752035 | benign | not provided | 2015-06-08 | criteria provided, single submitter | clinical testing |