ClinVar Miner

Variants studied for Parkinson disease

Coded as:
Minimum submission review status: Collection method:
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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 risk factor total
7 1 10 0 2 2 22

Gene and significance breakdown #

Total genes and gene combinations: 7
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign risk factor total
LRRK2 1 0 2 1 1 5
TNR 0 0 5 0 0 5
VPS13C 5 0 0 0 0 5
TNK2 0 1 3 0 0 4
GBA1, LOC106627981 0 0 0 0 1 1
RFC1 1 0 0 0 0 1
VPS35 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic likely pathogenic uncertain significance benign risk factor total
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 1 8 0 0 9
Brain and Spine Institute, INSERM 5 0 0 0 0 5
Molecular Genetics, Royal Melbourne Hospital 1 0 2 2 0 5
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 0 0 0 0 2 2
Research Unit of Clinical Medicine, Medical Research Center Oulu, University of Oulu 1 0 0 0 0 1

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