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
28	11	196	224	25	474

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	28	11	196	224	25	474

Submitter and significance breakdown #

Total submitters: 10

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Invitae	26	9	144	204	15	398
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
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	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.