Variants studied for Breast-ovarian cancer, familial, susceptibility to, 3; Fanconi anemia complementation group O

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
16	15	92	18	1	3	143

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	not provided	total
RAD51C	14	14	83	17	1	2	129
LOC129390903, RAD51C	2	1	9	1	0	1	14

Submitter and significance breakdown #

Total submitters: 5

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	13	12	82	13	0	0	120
Counsyl	6	5	14	5	1	0	31
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	3	3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	2	0	0	0	2
Juno Genomics, Hangzhou Juno Genomics, Inc	0	1	0	0	0	0	1

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