ClinVar Miner

Variants studied for Breast-ovarian cancer, familial 4

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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
37 35 256 54 5 6 379

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
RAD51D, RAD51L3-RFFL 36 35 254 54 5 4 374
RAD51D 1 0 0 0 0 2 3
FNDC8 0 0 1 0 0 0 1
FNDC8, RAD51D, RAD51L3-RFFL 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
Invitae 37 21 239 19 1 0 317
Counsyl 6 13 23 27 4 0 73
Mendelics 1 4 15 12 0 0 32
Fulgent Genetics,Fulgent Genetics 2 1 6 0 0 0 9
OMIM 0 0 0 0 0 6 6
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 1 0 2 0 3
University of Washington Department of Laboratory Medicine, University of Washington 0 0 0 1 0 0 1

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