ClinVar Miner

Submissions for variant NM_032043.2(BRIP1):c.2637A>G (p.Glu879=) (rs4986765)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 10
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000755226 SCV000602888 benign not provided 2017-05-01 criteria provided, single submitter clinical testing
Ambry Genetics RCV000162379 SCV000212689 benign Hereditary cancer-predisposing syndrome 2014-11-07 criteria provided, single submitter clinical testing
Color RCV000162379 SCV000537320 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
Counsyl RCV000410880 SCV000489871 benign Fanconi anemia, complementation group J 2016-06-18 criteria provided, single submitter clinical testing
Counsyl RCV000412411 SCV000489872 benign Neoplasm of ovary 2016-06-18 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000290016 SCV000404592 likely benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000347348 SCV000404593 likely benign Neoplasm of the breast 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000550975 SCV000633629 benign Familial cancer of breast; Fanconi anemia, complementation group J 2017-07-10 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000242120 SCV000538507 benign not specified 2016-03-29 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
PreventionGenetics RCV000242120 SCV000314838 benign not specified criteria provided, single submitter clinical testing

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.