ClinVar Miner

Variants studied for Parkinson disease 11

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 risk factor total
0 1 0 3 7 5 13

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic likely benign benign risk factor total
GIGYF2 1 3 7 5 13

Submitter and significance breakdown #

Total submitters: 5
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Submitter likely pathogenic likely benign benign risk factor total
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 0 1 6 0 7
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam 0 2 4 0 6
OMIM 0 0 0 5 5
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 0 0 5 0 5
UCLA Clinical Genomics Center, UCLA 1 0 0 0 1

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