ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.159-7C>T

gnomAD frequency: 0.00002  dbSNP: rs533403598
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
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, LLC DBA Color Health 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, LabCorp RCV002229526 SCV002511511 uncertain significance not specified 2022-04-25 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences 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).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.