rs34637584, LRRK2

N. diseases: 78
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
0.040 GeneticVariation BEFREE The G2019S mutation in leucine-rich repeat kinase 2 (<i>LRRK2</i>) is a prevalent cause of late-onset Parkinson's disease, producing psychiatric and motor symptoms, including depression, that are indistinguishable from sporadic cases. 30249796 2018
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
0.040 GeneticVariation BEFREE G2019S carriers do not manifest changes in gray matter volume or diffusivity parameters in Parkinson's disease-related structures prior to the appearance of motor symptoms. 24482120 2014
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
0.040 GeneticVariation BEFREE Like in IPD, disturbances such as hyposmia, depression, constipation and excessive daytime sleepiness may antedate the onset of classical motor symptoms in LRRK2-G2019S-PD. 25330404 2014
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
0.040 GeneticVariation BEFREE At the age of 80 years only one-half of G2019S mutation carriers manifest motor symptoms of PD. 21954089 2011