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
55	31	442	380	39	930

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	55	31	442	380	39	930

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Invitae	50	22	431	373	35	911
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
Genomics And Bioinformatics Analysis Resource, Columbia University	1	1	0	0	0	2
MGZ Medical Genetics Center	0	1	0	0	0	1
Department Of Translational Genomics (developmental Genetics Section), King Faisal Specialist Hospital & Research Centre	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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