ClinVar Miner

Variants studied for GM1 gangliosidosis type 2

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 not provided total
11 0 4 0 0 6 20

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance not provided total
GLB1 11 4 6 20

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic uncertain significance not provided total
Laboratory of Molecular Genetics MedGen 0 0 6 6
Mendelics 3 1 0 4
Counsyl 3 0 0 3
OMIM 2 0 0 2
Institute of Human Genetics,Klinikum rechts der Isar 2 0 0 2
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 2 0 0 2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 2 0 2
Baylor Genetics 1 0 0 1
Dr. Faghihi's Medical Genetic Center 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 1

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