List of variants in gene LRRK2 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.4872C>A (p.Gly1624=)	rs1427263	0.70218
NM_198578.4(LRRK2):c.7190T>C (p.Met2397Thr)	rs3761863	0.61824
NM_198578.4(LRRK2):c.4911A>G (p.Lys1637=)	rs11176013	0.56443
NM_198578.4(LRRK2):c.5457T>C (p.Gly1819=)	rs10878371	0.56374
NM_198578.4(LRRK2):c.457T>C (p.Leu153=)	rs10878245	0.50692
NM_198578.4(LRRK2):c.1102-10C>A	rs7955902	0.31995
NM_198578.4(LRRK2):c.6324G>A (p.Glu2108=)	rs10878405	0.26650
NM_198578.4(LRRK2):c.4193G>A (p.Arg1398His)	rs7133914

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.