Variants studied for Myofibrillar myopathy 5

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
6	5	19	2	0	1	33

Gene and significance breakdown #

Total genes and gene combinations: 1

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	not provided	total
FLNC	6	5	19	2	1	33

Submitter and significance breakdown #

Total submitters: 17

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	not provided	total
Baylor Genetics	1	3	5	0	0	9
OMIM	3	0	0	0	0	3
Mendelics	1	1	1	0	0	3
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	3	0	0	3
Phosphorus, Inc.	0	0	1	2	0	3
Centogene AG - the Rare Disease Company	0	0	2	0	0	2
Institute of Human Genetics, University of Leipzig Medical Center	2	0	0	0	0	2
Molecular Genetics, Royal Melbourne Hospital	0	0	2	0	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	1
Clinical Genomics Laboratory, Washington University in St. Louis	1	0	0	0	0	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	0	1	0	0	1
GenomeConnect, ClinGen	0	0	0	0	1	1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen	1	0	0	0	0	1
Breda Genetics srl	0	0	1	0	0	1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	1
Human Genetics Bochum, Ruhr University Bochum	0	0	1	0	0	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.