Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 GeneticVariation disease BEFREE While these results suggest that LRRK2 R1398H or N551K do not appear to modulate the risk of ET, it remains possible that a protective trend for both variants may be present in ET and a much larger sample size is required to identify this. 29593234 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 GeneticVariation disease BEFREE The data suggest that LRRK1 variant (rs2924835) and LRRK2 variants (rs34594498, rs34410987, and rs33949390) are not associated with ET in this Han Chinese population. 29812962 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 GeneticVariation disease BEFREE Using a case control methodology, we demonstrated an association between a known PD risk variant, LRRK2 R1628P, with ET. 25761573 2015
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 Biomarker disease BEFREE LRRK2 mutations were not found in any ET cases or ET brains and none of the LRRK2 SNPs was associated with ET. 19527940 2010
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 Biomarker disease LHGDN Common mutations in the LRRK2 exon 41 are not responsible for essential tremor in Italian patients. 18556235 2009
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 GeneticVariation disease BEFREE The LRRK2 Gly2385Arg variant is not a significant risk factor for ET in our population. 18316234 2008
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 GeneticVariation disease BEFREE To evaluate the frequency of the LRRK2 P755L variant in North American Caucasian patients with PD, we screened 426 PD patients and 37 additional patients with the combination of PD and essential tremor (ET) from our Parkinson Disease Center and Movement Clinic at Baylor College of Medicine. 17482357 2007
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2
0.080 GeneticVariation disease BEFREE Since phenotypes of PD overlap with essential tremor (ET), we investigated LRRK2 G2019S, I2012T, and I2020T mutations in a cohort of 272 patients with ET. 16939701 2006