rs34637584, LRRK2

N. diseases: 78
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.040 GeneticVariation BEFREE The results showed that LRRK2 variants (p.R1628P, p.G2385R, p.N551K, p.G2019S, and p.I2020T) were not associated with the risk of AD and were not a common cause of AD in populations. 31038182 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.040 GeneticVariation BEFREE Such suggestions are relevant mainly for people at putatively high risk of developing AD (i.e., older adults with mild cognitive impairment subtypes) or PD (i.e., older adults with either Mild Parkinsonian signs or LRRK2 G2019S mutation). 28588547 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.040 GeneticVariation BEFREE We screened the most common LRRK2 mutation (p.G2019S) in a series of 180 consecutive patients clinically diagnosed with Alzheimer Disease (AD). 19822953 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
0.040 GeneticVariation BEFREE No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 17846883 2007