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 1 0 3 2 6

Gene and significance breakdown #

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

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance benign risk factor total
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 3 0 3
OMIM 0 0 2 2
Baylor Genetics 1 0 0 1

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