Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000663238 | SCV000786442 | uncertain significance | Familial cancer of breast | 2018-05-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000663238 | SCV001670266 | likely benign | Familial cancer of breast | 2018-02-08 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV000663238 | SCV004020074 | uncertain significance | Familial cancer of breast | 2023-03-07 | criteria provided, single submitter | clinical testing | This variant is classified as a variant of uncertain significance as there is insufficient evidence to determine its impact on protein function and/or cancer risk. |