ClinVar Miner

Variants studied for Glycogen storage disease XV

Coded as:
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 total
4 0 1 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance total
GYG1 4 1 5

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance total
OMIM 2 0 2
Undiagnosed Diseases Network, NIH 2 0 2
Baylor Genetics 1 0 1
MGZ Medical Genetics Center 1 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 1
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 1 0 1

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