Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3129882
rs3129882
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
0.900 GeneticVariation BEFREE In current meta-analysis, no significant association was found for rs3129882 and PD risk. 25720714 2015
dbSNP: rs3129882
rs3129882
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
0.900 GeneticVariation BEFREE The results suggest that rs3129882 polymorphism may be a risk factor for PD in Iranian. 25319953 2014
dbSNP: rs3129882
rs3129882
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
0.900 GeneticVariation BEFREE We observed no association between PD risk and GAK rs1564282 or HLA-DRA rs3129882 variant. 24039160 2013
dbSNP: rs3129882
rs3129882
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
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
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0030567
Disease:
Parkinson Disease
G 0.900 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177 2010
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE DNA was extracted from blood in order to analyse EBV and HHV-6 viral load by quantitative real-time polymerase chain reaction and to genotype MS-related single nucleotide polymorphisms (rs3135388, rs2248359 and rs12368653) when possible. 29996002 2018
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE Presence of the rs3135388 polymorphism tagging the major MS risk allele HLA-DRB1*15:01 allele was determined as well. 28130760 2017
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE We genotyped a cohort of 1033 MS patients and 644 healthy controls with a consistent genetic background for the 57 non-MHC variants reported to be associated with MS by the first large GWAS as well as the HLA DRB1*1501 tagging SNP rs3135388. 26011527 2015
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE Our findings show for the first time that the rs3135388</span> polymorphism is a strong risk factor for MS in the Slovak population. 25958306 2015
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
A 0.890 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE Our results indicate that the distribution of the rs3135388 gene polymorphism is a risk factor for MS susceptibility in the Czech female population. 23186557 2013
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE We analyzed the allelic and genotype frequency of VDR rs2228570, rs731236, and HLADRB1*1501 (rs3135388) in 303 patients with MS and 310 healthy controls, using TaqMan Assays. 23840333 2013
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE We observed a trend for association of rs3135388 (HLA-DRB1*1501, p < 0.01), rs7090530 (IL2RA, p < 0.026) and rs1841770 (ZIC1, p < 0.017) with a younger age at MS onset and of rs12044852 (CD58, p < 0.035) with shorter time to reach EDSS6. 22411505 2012
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
0.890 GeneticVariation BEFREE In quantitative terms, the MS-risk AA genotype carriers of rs3135388 were associated with 15.7-, 5.2- and 8.3-fold higher expression of DQB1, DRB5 and DRB1, respectively, than the non-risk GG carriers. 22253788 2012
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
A 0.890 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953 2009
dbSNP: rs3135388
rs3135388
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease:
Multiple Sclerosis
A 0.890 GeneticVariation GWASCAT Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953 2009