ClinVar Miner

Variants studied for Familial cancer of breast; Fanconi anemia complementation group J

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 not provided total
457 170 2325 1236 44 1 4205

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
BRIP1 450 169 2316 1236 44 1 4188
BRIP1, LOC130061360 4 0 4 0 0 0 8
BRIP1, LOC110120932, LOC130061360 1 0 4 0 0 0 5
BRIP1, INTS2 2 0 0 0 0 0 2
BRIP1, LOC110120932 0 1 1 0 0 0 2

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 455 155 2311 1233 44 0 4198
Fulgent Genetics, Fulgent Genetics 15 14 75 4 2 0 110
Department of Pathology and Laboratory Medicine, Sinai Health System 2 2 1 3 1 0 9
Juno Genomics, Hangzhou Juno Genomics, Inc 1 3 0 0 0 0 4
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 1 1

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