ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2258-13T>C

dbSNP: rs1567779896
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
Color Diagnostics, LLC DBA Color Health RCV000776989 SCV000912664 likely benign Hereditary cancer-predisposing syndrome 2017-12-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067348 SCV002335856 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-08-19 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004788183 SCV005404067 likely benign Familial cancer of breast 2024-09-04 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.