List of variants in gene LRRK2 reported as benign by Fulgent Genetics, Fulgent Genetics

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:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.4939T>A (p.Ser1647Thr)	rs11564148	0.26687
NM_198578.4(LRRK2):c.6324G>A (p.Glu2108=)	rs10878405	0.26650
NM_198578.4(LRRK2):c.1653C>G (p.Asn551Lys)	rs7308720	0.10004
NM_198578.4(LRRK2):c.2857T>C (p.Leu953=)	rs7966550	0.08994
NM_198578.4(LRRK2):c.4269G>A (p.Lys1423=)	rs11175964	0.05959
NM_198578.4(LRRK2):c.3778-9C>T	rs114948984	0.01375
NM_198578.4(LRRK2):c.4541G>A (p.Arg1514Gln)	rs35507033	0.00526
NM_198578.4(LRRK2):c.3497-8del	rs201739149
NM_198578.4(LRRK2):c.6844-8dup	rs72546334

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