Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2395163
rs2395163 		0.820 GeneticVariation GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012
dbSNP: rs2395163
rs2395163 		0.820 GeneticVariation BEFREE Similarly, rs3129882 and the closely linked rs9268515 and rs2395163 remained significant irrespective of HLA alleles. rs3129882 and rs2395163 are expression quantitative trait loci (eQTLs) for HLA-DR and HLA-DQ (9 × 10(-5) ≥ PeQTL ≥ 2 × 10(-79)), suggesting that HLA gene expression might influence PD. 24183452

2013
dbSNP: rs2395163
rs2395163 		0.820 GeneticVariation GWASCAT Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012
dbSNP: rs2395163
rs2395163 		0.820 GeneticVariation BEFREE The frequency of rs2395163 C allele (8.65%) in male patients with PD was significantly lower than in male control subjects (14.02%; OR = 0.58, 95% CI: 0.39-0.88, p = 0.009). 31818508

2020
dbSNP: rs2338971
rs2338971 		C 0.810 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014
dbSNP: rs2338971
rs2338971 		0.810 GeneticVariation BEFREE This study revealed the first evidence of the association of rs2338971 with increased risk of PD in the Iranian population. 26732583

2016
dbSNP: rs2338971
rs2338971 		C 0.810 GeneticVariation GWASCAT Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014
dbSNP: rs12063142
rs12063142 		0.800 GeneticVariation GWASCAT Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
dbSNP: rs12063142
rs12063142 		0.800 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
dbSNP: rs1296028
rs1296028 		0.800 GeneticVariation GWASCAT Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012
dbSNP: rs1296028
rs1296028 		0.800 GeneticVariation GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012
dbSNP: rs1630500
rs1630500 		0.800 GeneticVariation GWASCAT Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889

2014
dbSNP: rs1630500
rs1630500 		0.800 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889

2014
dbSNP: rs6532194
rs6532194 		0.800 GeneticVariation GWASCAT Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs6532194
rs6532194 		0.800 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs6532197
rs6532197 		G 0.800 GeneticVariation GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs6532197
rs6532197 		G 0.800 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs6532197
rs6532197 		0.800 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012
dbSNP: rs823118
rs823118 		0.730 GeneticVariation BEFREE However, we could not confirm the association of rs12456492 and rs823118 with PD. 31818509

2020
dbSNP: rs823118
rs823118 		0.730 GeneticVariation BEFREE Here, in order to discover potential AD-related loci, we investigated the association between late-onset AD (LOAD) susceptibility and nine single-nucleotide polymorphisms (SNPs) (rs11724635 of BST1, rs12637471 of MCCC1, rs15553999 of TMEM229, rs17649553 of MAPT, rs34311866 of TMEM175-GAK-DGKQ, rs356182 of SNCA, rs6430538 of ACMSD-TMEM163, rs76904798 of LRRK2 and rs823118 of RAB7L1-NUCKS1) which were reported to have genome-wide significant associations with PD risk in a recent Genome Wide Association Study performed among white population. 26738859

2017
dbSNP: rs823118
rs823118 		0.730 GeneticVariation BEFREE Our study provides strong support for the susceptibility role of rs823118 and rs12637471 in sporadic PD in a Han Chinese population. 26914237

2016
dbSNP: rs823118
rs823118 		T 0.730 GeneticVariation GWASCAT A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. 28892059

2017
dbSNP: rs823118
rs823118 		0.730 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs823118
rs823118 		T 0.730 GeneticVariation GWASCAT Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. 25064009

2014
dbSNP: rs9468199
rs9468199 		0.720 GeneticVariation BEFREE Therefore, we performed a replication study of 5 of the most commonly identified candidate variants, including SORBS3 rs2280104, SCN3A rs353116, TOX3 rs4784227, GLAC rs8005172, and ZNF184 rs9468199, in a large sample of patients with PD (1506) and multiple system atrophy (MSA, 496) in a Chinese population. 29691093

2018