ClinVar Miner

Variants from Cancer Genetics and Genomics Laboratory, British Columbia Cancer Agency

Location: Canada  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 total
24 0 29 17 69 139

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic uncertain significance likely benign benign total
BRCA2 17 20 2 46 85
BRCA1 6 7 15 21 49
BRCA1, LOC126862571 1 2 0 2 5

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic uncertain significance likely benign benign total
not specified 0 1 17 69 87
Hereditary breast ovarian cancer syndrome 24 28 0 0 52

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