ClinVar Miner

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

Location: United States  Primary collection method: clinical testing
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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: 4
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Gene or gene combination pathogenic uncertain significance benign not provided total
BRCA1 703 724 27 32 1482
BRCA1, LOC126862571 143 104 8 2 257
​intergenic 0 2 0 0 2
BRCA1, LOC111589215 0 1 0 0 1

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic uncertain significance benign not provided total
Breast-ovarian cancer, familial, susceptibility to, 1 846 831 35 34 1742

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