Variants studied for Osteochondritis dissecans

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
8	5	13	2	21	49

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
ACAN	8	5	13	2	21	49

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Genome-Nilou Lab	0	0	0	0	21	21
Institute of Human Genetics, University of Leipzig Medical Center	0	1	5	0	0	6
Mendelics	1	0	0	2	1	4
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	0	1	2	0	0	3
Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital	2	1	0	0	0	3
Baylor Genetics	0	0	2	0	0	2
Institute of Human Genetics, University of Goettingen	1	0	0	0	0	1
Fulgent Genetics, Fulgent Genetics	0	0	1	0	0	1
Illumina Laboratory Services, Illumina	1	0	0	0	0	1
Hadassah Hebrew University Medical Center	1	0	0	0	0	1
Bicknell laboratory, University of Otago	0	0	1	0	0	1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	1	0	0	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	1	0	0	0	0	1
Genetics and Molecular Pathology, SA Pathology	1	0	0	0	0	1
Breda Genetics srl	0	0	1	0	0	1
Shieh Lab, University of California, San Francisco	0	1	0	0	0	1
3billion	0	0	1	0	0	1

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