Variants studied for Mirror movements 1

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	not provided	total
13	5	7	0	6	12	37

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	not provided	total
DCC	13	5	6	6	12	36
DCC, MIR4528	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	not provided	total
GeneReviews	1	0	0	0	12	13
OMIM	8	0	0	0	0	8
Genome-Nilou Lab	0	0	0	6	0	6
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	1	2	0	0	0	3
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	2	1	0	0	3
Baylor Genetics	0	0	2	0	0	2
Mendelics	0	0	1	1	0	2
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	1
Geisinger Autism and Developmental Medicine Institute, Geisinger Health System	0	0	1	0	0	1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota	0	1	0	0	0	1
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine	1	0	0	0	0	1
Institute of Medical Genetics, Medical University of Vienna	1	0	0	0	0	1
Molecular Genetics, Royal Melbourne Hospital	1	0	0	0	0	1

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