List of variants in gene LRRK2 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 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.4321C>T (p.Arg1441Cys)	rs33939927	0.00003
NM_198578.4(LRRK2):c.4310A>G (p.Asn1437Ser)	rs1944946235
NM_198578.4(LRRK2):c.6059T>C (p.Ile2020Thr)	rs35870237

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