ClinVar Miner

Variants studied for glycogen storage disease VI

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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
38 23 111 74 30 18 255

Gene and significance breakdown #

Total genes and gene combinations: 2
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
PYGL 38 23 111 74 29 18 254
LOC130055618, PYGL 0 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 25
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 21 5 66 67 24 0 183
Illumina Laboratory Services, Illumina 0 1 36 4 17 0 58
GeneReviews 1 0 0 0 0 18 19
Neuberg Centre For Genomic Medicine, NCGM 2 5 4 0 0 0 11
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 1 5 4 0 10
Baylor Genetics 2 0 6 0 0 0 8
Fulgent Genetics, Fulgent Genetics 0 0 6 0 2 0 8
Genome-Nilou Lab 0 0 0 0 7 0 7
Revvity Omics, Revvity 1 2 3 0 0 0 6
Molecular Diagnostics Laboratory, Seoul National University Hospital 1 5 0 0 0 0 6
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 4 1 0 0 0 6
OMIM 5 0 0 0 0 0 5
Mendelics 2 1 1 0 1 0 5
Centre for Human Genetics 3 0 2 0 0 0 5
3billion 1 0 4 0 0 0 5
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 3 1 0 0 0 0 4
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 1 0 0 0 2
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 1 0 0 0 0 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 1 0 0 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 0 0 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 0 1
Pathology and Clinical Laboratory Medicine, King Fahad Medical City 1 0 0 0 0 0 1
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 1 1
Suma Genomics, Suma Genomics 1 0 0 0 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.