ClinVar Miner

Variants studied for Gaucher disease type III

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
37 19 13 5 0 1 72

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign not provided total
GBA1, LOC106627981 35 19 10 5 1 67
GBA1 2 0 3 0 0 5

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance likely benign not provided total
Fulgent Genetics, Fulgent Genetics 23 6 10 4 0 43
Baylor Genetics 21 8 0 0 0 29
OMIM 12 0 0 0 0 12
Juno Genomics, Hangzhou Juno Genomics, Inc 4 3 1 0 0 8
3billion 1 0 0 1 0 2
Otogenetics 1 1 0 0 0 2
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) 1 0 0 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 0 1 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 1 0 0 1
GenomeConnect, ClinGen 0 0 0 0 1 1
Johns Hopkins Genomics, Johns Hopkins University 0 1 0 0 0 1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 1 0 0 0 0 1
PreventionGenetics, part of Exact Sciences 0 1 0 0 0 1

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