List of variants in gene COQ2 reported as risk factor for synucleinopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001358921.2(COQ2):c.1010G>A (p.Arg337Gln)	rs763562410	0.00002
NM_001358921.2(COQ2):c.1009C>T (p.Arg337Ter)	rs751185256	0.00001
NM_001358921.2(COQ2):c.878T>C (p.Val293Ala)	rs397514727

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