Variants studied for Parkinson Disease, Dominant

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
0	0	79	15	20	114

Gene and significance breakdown #

Total genes and gene combinations: 5

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Gene or gene combination	uncertain significance	likely benign	benign	total
SNCA	63	11	19	93
VPS35	16	1	0	17
ORC6, VPS35	0	1	1	2
LRRK2	0	1	0	1
UCHL1	0	1	0	1

Submitter and significance breakdown #

Total submitters: 1

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Submitter	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	79	15	20	114

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