Variants studied for Cataract 18

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
18	3	154	54	74	282

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
FYCO1	18	3	154	54	74	282

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	116	20	59	195
Invitae	7	0	43	38	50	138
Genome-Nilou Lab	0	0	0	0	13	13
OMIM	6	0	0	0	0	6
Fulgent Genetics, Fulgent Genetics	0	0	1	2	0	3
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	2	0	0	0	0	2
Institute of Human Genetics, University of Leipzig Medical Center	1	1	0	0	0	2
Baylor Genetics	0	0	1	0	0	1
Revvity Omics, Revvity	1	0	0	0	0	1
MGZ Medical Genetics Center	1	0	0	0	0	1
Intergen, Intergen Genetics and Rare Diseases Diagnosis Center	0	0	0	1	0	1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	1	0	0	0	1
Laboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems	0	1	0	0	0	1

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