ClinVar Miner

Variants from Cancer Genetics Laboratory,Peter MacCallum Cancer Centre

Location: Australia — Primary collection method: case-control
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
0 19 42 35 0 96

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic uncertain significance likely benign total
PALB2 19 42 35 96

Condition and significance breakdown #

Total conditions: 1
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Condition likely pathogenic uncertain significance likely benign total
Familial cancer of breast 19 42 35 96

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