ClinVar Miner

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

Coded as:
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
181 65 1168 243 28 1680

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
BRIP1 180 64 1163 243 28 1673
BRIP1, LOC110120932 1 1 5 0 0 7

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 180 65 1163 243 28 1679
Fulgent Genetics,Fulgent Genetics 4 0 17 0 0 21

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