List of variants in gene VPS35 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
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_018206.6(VPS35):c.*283del	rs886052005	0.07609
NM_018206.6(VPS35):c.259_260dup	rs886052011	0.00001
NM_018206.6(VPS35):c.*258del	rs886052012
NM_018206.6(VPS35):c.275_276insCAA	rs886052010
NM_018206.6(VPS35):c.276_277insCAA	rs886052008
NM_018206.6(VPS35):c.277_278insCA	rs886052007
NM_018206.6(VPS35):c.278_279insCAA	rs575317929
NM_018206.6(VPS35):c.279_280insCAAA	rs886052006
NM_018206.6(VPS35):c.*281CA[1]	rs879039152
NM_018206.6(VPS35):c.*281delinsAAAA	rs1555522775
NM_018206.6(VPS35):c.*281delinsAAAAA	rs1555522775
NM_018206.6(VPS35):c.285_287dup	rs369068093
NM_018206.6(VPS35):c.287_288insAAAC	rs1555522760
NM_018206.6(VPS35):c.287_288insAAC	rs1555522760
NM_018206.6(VPS35):c.*287dup	rs369068093
NM_018206.6(VPS35):c.761_762dup	rs34926621
NM_018206.6(VPS35):c.*762dup	rs34926621

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