Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11931074
rs11931074
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs11931074
rs11931074
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs11931074
rs11931074
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

dbSNP: rs11931074
rs11931074
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
G 0.900 GeneticVariation GWASDB Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576

2009

dbSNP: rs3129882
rs3129882
CUI: C0030567
Disease: Parkinson 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
CUI: C0030567
Disease: Parkinson 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: rs34637584
rs34637584
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889

2014

dbSNP: rs34637584
rs34637584
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
A 0.900 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs34778348
rs34778348
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs356219
rs356219
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014

dbSNP: rs356219
rs356219
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs356219
rs356219
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
G 0.900 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011

dbSNP: rs356219
rs356219
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.900 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs12456492
rs12456492
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.890 GeneticVariation GWASDB A novel PD susceptibility locus, RIT2, on chromosome 18 (rs12456492; p=5×10(-5) Discovery Sample; p=1.52×10(-7) Replication sample; p=2×10(-10) Combined Sample) was replicated. 22451204

2012

dbSNP: rs11724635
rs11724635
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.880 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs11724635
rs11724635
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.880 GeneticVariation GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012

dbSNP: rs11724635
rs11724635
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
A 0.880 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011

dbSNP: rs6812193
rs6812193
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
C 0.880 GeneticVariation GWASDB We discovered two novel, genome-wide significant associations with PD-rs6812193 near SCARB2 (p = 7.6 × 10(-10), OR = 0.84) and rs11868035 near SREBF1/RAI1 (p = 5.6 × 10(-8), OR = 0.85)-both replicated in an independent cohort. 21738487

2011

dbSNP: rs6812193
rs6812193
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
T 0.880 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009

dbSNP: rs1564282
rs1564282
GAK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.870 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs1564282
rs1564282
GAK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.870 GeneticVariation GWASDB Microarray expression analysis of post-mortem frontal cortex from PD and control brains demonstrates a significant association between rs1564282 and higher α-synuclein expression, a known cause of early onset PD. 21258085

2011

dbSNP: rs2736990
rs2736990
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.860 GeneticVariation GWASDB Identification of a novel Parkinson's disease locus via stratified genome-wide association study. 24511991

2014

dbSNP: rs2736990
rs2736990
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.860 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs2736990
rs2736990
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.860 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs2736990
rs2736990
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.860 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010