Variants studied for Senior-Loken syndrome 8

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
56	32	443	380	39	933

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
WDR19	56	32	443	380	39	933

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	51	22	431	373	35	912
Fulgent Genetics, Fulgent Genetics	1	7	74	31	1	114
Genome-Nilou Lab	0	0	0	0	21	21
OMIM	8	0	0	0	0	8
Ocular Genomics Institute, Massachusetts Eye and Ear	1	0	2	0	0	3
Molecular Biology Laboratory, Fundació Puigvert	1	2	0	0	0	3
Baylor Genetics	2	0	0	0	0	2
Institute of Human Genetics, Cologne University	0	0	2	0	0	2
Juno Genomics, Hangzhou Juno Genomics, Inc	0	1	1	0	0	2
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	0	2	0	0	2
Genomics And Bioinformatics Analysis Resource, Columbia University	1	1	0	0	0	2
MGZ Medical Genetics Center	0	1	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	0	0	0	0	1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City	0	1	0	0	0	1
Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University	0	0	1	0	0	1

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