ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1341-12A>G

gnomAD frequency: 0.00001  dbSNP: rs1441257544
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002112364 SCV002389943 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2023-12-17 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003585209 SCV004362942 likely benign Hereditary cancer-predisposing syndrome 2023-02-16 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004793728 SCV005406581 likely benign Familial cancer of breast 2024-08-27 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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.