Variants studied for Mitochondrial complex III deficiency nuclear type 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
6	3	6	0	0	13

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
LYRM7	6	3	6	13

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
OMIM	5	0	0	5
Revvity Omics, Revvity	0	1	2	3
Baylor Genetics	0	0	1	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	0	1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen	0	1	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	1	0	0	1
Myelin Disorders Clinic-Children's Medical Center/Medical Genetics Lab-Tarbiat Modares University, Children's Medical Center, Pediatrics Center of Excellence,	0	0	1	1
Lifecell International Pvt. Ltd	0	1	0	1
3billion	0	0	1	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	1

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