Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000206858 | SCV000260963 | likely benign | Familial cancer of breast | 2023-12-26 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000583460 | SCV000688136 | likely benign | Hereditary cancer-predisposing syndrome | 2016-02-24 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV002229526 | SCV002511511 | uncertain significance | not specified | 2022-04-25 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003897450 | SCV004716851 | likely benign | BARD1-related condition | 2022-09-30 | criteria provided, single submitter | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |