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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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	not provided	total
401	149	2180	1116	43	1	3875

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	not provided	total
BRIP1	397	148	2170	1116	43	1	3860
BRIP1, LOC130061360	3	0	5	0	0	0	8
BRIP1, LOC110120932, LOC130061360	1	0	4	0	0	0	5
BRIP1, LOC110120932	0	1	1	0	0	0	2

Submitter and significance breakdown #

Total submitters: 3

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Invitae	400	146	2172	1114	43	0	3875
Fulgent Genetics, Fulgent Genetics	7	4	32	4	2	0	49
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	1	1

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