ClinVar Miner

Variants from Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto

Location: Canada  Primary collection method: research
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
913 9 75 0 24 2 1023

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign not provided total
BRCA2 451 2 34 10 0 497
BRCA1 379 7 37 12 1 436
BRCA1, LOC126862571 83 0 4 2 1 90

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic likely pathogenic uncertain significance benign not provided total
Hereditary breast ovarian cancer syndrome 913 9 0 0 0 922
not specified 0 0 75 24 2 101

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