Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35870237
rs35870237
0.010 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 a</span>nd were not a common cause of AD in populations. 31038182

2019