Variants studied for Fanconi anemia complementation group L

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	total
10	35	76	18	10	140

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
FANCL	9	34	67	15	9	127
FANCL, VRK2	1	1	9	3	1	13

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	0	3	38	12	2	55
Illumina Laboratory Services, Illumina	0	1	32	4	7	44
Baylor Genetics	3	30	10	0	0	43
KCCC/NGS Laboratory, Kuwait Cancer Control Center	0	0	0	2	5	7
OMIM	5	0	0	0	0	5
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	1	4	0	0	5
Revvity Omics, Revvity	1	0	3	0	0	4
Leiden Open Variation Database	2	1	0	0	0	3
Center for Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong University	0	2	0	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	2	0	0	0	0	2
Genetic Services Laboratory, University of Chicago	1	0	0	0	0	1
Hadassah Hebrew University Medical Center	0	0	0	1	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	1	0	0	0	0	1
Daryl Scott Lab, Baylor College of Medicine	0	0	1	0	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
3billion	0	1	0	0	0	1

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