ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.441+8C>T

gnomAD frequency: 0.00001  dbSNP: rs756130118
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 RCV001180530 SCV001345470 uncertain significance Hereditary cancer-predisposing syndrome 2019-06-07 criteria provided, single submitter clinical testing
Genetics Program, Instituto Nacional de Cancer RCV002307691 SCV002515264 uncertain significance Hereditary breast ovarian cancer syndrome 2021-11-01 criteria provided, single submitter research
Labcorp Genetics (formerly Invitae), Labcorp RCV002307691 SCV003348157 likely benign Hereditary breast ovarian cancer syndrome 2022-05-06 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.