ClinVar Miner

Variants studied for Autosomal recessive Parkinson disease 14

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 total
8 3 2 0 0 12

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
PLA2G6 8 3 2 12

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance total
OMIM 6 0 0 6
Genomics England Pilot Project, Genomics England 1 3 0 4
Department of Neurology, Xijing Hospital, Fourth Military Medical University 1 0 1 2
Baylor Genetics 1 0 0 1
MGZ Medical Genetics Center 0 0 1 1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 1 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 1 0 1
Lifecell International Pvt. Ltd 1 0 0 1
3billion 1 0 0 1

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