ClinVar Miner

Variants studied for Polyglucosan body myopathy type 2

Coded as:
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Gene type:
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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
5 4 2 0 0 9

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
GYG1 5 2 2 7
GYG1, LOC129937737 0 2 0 2

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance total
OMIM 5 0 0 5
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 2 0 3
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 1 1 0 2
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 1 2
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 1 1 0 2
Baylor Genetics 1 0 0 1
MGZ Medical Genetics Center 0 1 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 1

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