List of variants in gene LRRK2 reported as likely pathogenic for Autosomal dominant Parkinson disease 8

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.6055G>A (p.Gly2019Ser)	rs34637584	0.00036
NM_198578.4(LRRK2):c.3974G>A (p.Arg1325Gln)	rs72546338	0.00021
NM_198578.4(LRRK2):c.4322G>A (p.Arg1441His)	rs34995376	0.00001
NM_198578.4(LRRK2):c.4321C>A (p.Arg1441Ser)	rs33939927

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