Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE The results of this meta-analysis suggest that HLA-DRA rs3129882 A/G polymorphism was not responsible for PD in Chinese-based populations. 24849299

2015
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE In current meta-analysis, no significant association was found for rs3129882 and PD risk. 25720714

2015
dbSNP: rs3129882
rs3129882
HLA-DRA
G 0.900 GeneticVariation GWASDB HLA_rs3129882 was more strongly associated with Sporadic-PD (OR = 1.38, P = 5 × 10(-10)) than Familial-PD (OR = 1.12, P = 0.15). 24511991

2014
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE HLA_rs3129882 was more strongly associated with Sporadic-PD (OR = 1.38, P = 5 × 10(-10)) than Familial-PD (OR = 1.12, P = 0.15). 24511991

2014
dbSNP: rs3129882
rs3129882
HLA-DRA
G 0.900 GeneticVariation GWASCAT HLA_rs3129882 was more strongly associated with Sporadic-PD (OR = 1.38, P = 5 × 10(-10)) than Familial-PD (OR = 1.12, P = 0.15). 24511991

2014
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE The results suggest that rs3129882 polymorphism may be a risk factor for PD in Iranian. 25319953

2014
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE Genetic interaction analysis revealed that subjects simultaneously carrying the T allele (TC or TT) of rs11248051 and the A allele (AG or AA) of rs3129882 had an aggravated risk (OR 1.91; p=0.016) of PD. 24373818

2014
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 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: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE A variant (rs3129882) in the genome-wide association study (GWAS)-linked variant [in the human leukocyte antigen (HLA) gene region] has been reported to associate with an increased risk of Parkinson's disease (PD) in Caucasian population.Studies among Chinese are limited. 23083294

2013
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE We observed no association between PD risk and GAK rs1564282 or HLA-DRA rs3129882 variant. 24039160

2013
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE A recent genome-wide association study (GWAS) reported an association between HLA-DRA rs3129882 and the development of PD in Caucasian populations. 22243834

2012
dbSNP: rs3129882
rs3129882
HLA-DRA
0.900 GeneticVariation BEFREE Herein, we evaluated the association between rs3129882 and PD in </span>three different Caucasian patient-control series (combined 1313 patients and 1305 controls) from the US, Ireland, and Poland. 21482477

2011
dbSNP: rs3129882
rs3129882
HLA-DRA
G 0.900 GeneticVariation GWASCAT Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs3129882
rs3129882
HLA-DRA
G 0.900 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010