ClinVar Miner

Variants studied for Breast-ovarian cancer, familial 4

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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 risk factor total
34 27 198 104 12 6 360

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
RAD51D, RAD51L3-RFFL 33 27 197 104 12 2 354
RAD51D 1 0 0 0 0 4 5
FNDC8, RAD51D, RAD51L3-RFFL 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
Invitae 33 15 190 82 9 0 329
Counsyl 6 13 23 27 4 0 73
Fulgent Genetics 2 1 6 0 0 0 9
OMIM 0 0 0 0 0 6 6
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics 1 0 0 0 0 0 1
University of Washington Department of Laboratory Medicine,University of Washington 0 0 0 1 0 0 1

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