Variants studied for Oculodentodigital dysplasia

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
21	9	43	5	19	96

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
GJA1	21	9	43	5	19	96

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	41	5	19	65
OMIM	14	0	0	0	0	14
Genetic Services Laboratory, University of Chicago	2	2	0	0	0	4
Baylor Genetics	1	0	1	0	0	2
3billion	0	2	0	0	0	2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	0	1	0	0	0	1
MyeliNeuroGene Lab, McGill University Health Center Research Institute	1	0	0	0	0	1
Mendelics	0	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	1	0	0	0	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	0	0	0	1
Duke University Health System Sequencing Clinic, Duke University Health System	1	0	0	0	0	1
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	1	0	0	0	1
Daryl Scott Lab, Baylor College of Medicine	1	0	0	0	0	1
New York Genome Center	0	1	0	0	0	1
Paris Brain Institute, Inserm - ICM	1	0	0	0	0	1
Genomics England Pilot Project, Genomics England	0	1	0	0	0	1

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