Variants studied for autosomal recessive Parkinson disease 14

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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	total
14	8	26	1	0	45

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	total
PLA2G6	14	8	26	1	45

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	total
Fulgent Genetics, Fulgent Genetics	6	3	24	1	34
OMIM	6	0	0	0	6
Genomics England Pilot Project, Genomics England	1	3	0	0	4
Molecular Genetics Lab, CHRU Brest	0	2	0	0	2
Department of Neurology, Xijing Hospital, Fourth Military Medical University	1	0	1	0	2
Baylor Genetics	1	0	0	0	1
MGZ Medical Genetics Center	0	0	1	0	1
Mayo Clinic Laboratories, Mayo Clinic	1	0	0	0	1
Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München	1	0	0	0	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	1	0	0	1
Lifecell International Pvt. Ltd	1	0	0	0	1
3billion	1	0	0	0	1
Coban-Akdemir Lab, University of Texas Health Science Center	0	0	1	0	1

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