ClinVar Miner

Variants from Breast Cancer Information Core (BIC) (BRCA1)

Location: United States — Primary collection method: clinical testing
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
846 0 831 0 35 34 1742

Gene and significance breakdown #

Total genes and gene combinations: 3
Download table as spreadsheet
Gene or gene combination pathogenic uncertain significance benign not provided total
BRCA1 846 828 35 34 1739
​intergenic 0 2 0 0 2
BRCA1, LOC111589215 0 1 0 0 1

Condition and significance breakdown #

Total conditions: 1
Download table as spreadsheet
Condition pathogenic uncertain significance benign not provided total
Breast-ovarian cancer, familial 1 846 831 35 34 1742

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.