ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.3392G>A (p.Arg1131Lys) (rs1555283214)

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
CeGaT Praxis fuer Humangenetik Tuebingen RCV000585336 SCV000692770 uncertain significance not provided 2017-10-31 criteria provided, single submitter clinical testing
Color RCV000678992 SCV000905655 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-04 criteria provided, single submitter clinical testing
True Health Diagnostics RCV000678992 SCV000805240 likely benign Hereditary cancer-predisposing syndrome 2018-05-29 no assertion criteria provided 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.