Variants studied for Autosomal recessive limb-girdle muscular dystrophy type 2F

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
31	12	196	251	25	505

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	benign	total
SGCD	31	12	196	251	25	505

Submitter and significance breakdown #

Total submitters: 10

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	29	10	144	231	15	429
Genome-Nilou Lab	2	3	98	36	12	151
OMIM	5	0	0	0	0	5
Mendelics	0	0	0	0	2	2
Baylor Genetics	0	0	1	0	0	1
Athena Diagnostics	0	0	0	0	1	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	1	0	0	0	0	1
CSER _CC_NCGL, University of Washington	0	0	0	1	0	1
Myriad Genetics, Inc.	0	1	0	0	0	1
New York Genome Center	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.