ClinVar Miner

Variants from Michigan Medical Genetics Laboratories,University of Michigan

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 total
90 2 46 43 140 321

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
BRCA2 48 2 34 32 91 207
BRCA1 42 0 12 11 49 114

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Breast-ovarian cancer, familial 2 48 2 34 32 91 207
Breast-ovarian cancer, familial 1 42 0 12 11 49 114

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