ClinVar Miner

Variants studied for Parkinson disease 18, autosomal dominant, susceptibility to

Included ClinVar conditions (1):
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 risk factor total
0 0 6 3 3 2 14

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination uncertain significance likely benign benign risk factor total
EIF4G1 6 3 3 2 14

Submitter and significance breakdown #

Total submitters: 9
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Submitter uncertain significance likely benign benign risk factor total
Fulgent Genetics, Fulgent Genetics 1 3 0 0 4
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 3 0 3
OMIM 0 0 0 2 2
Baylor Genetics 1 0 0 0 1
Institute of Human Genetics, University of Goettingen 1 0 0 0 1
Suna and Inan Kirac Foundation Neurodegeneration Research Laboratory, Koc University 1 0 0 0 1
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 1 0 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 1 0 0 0 1

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