Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs356168
rs356168
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010

dbSNP: rs356168
rs356168
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.710 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs3857053
rs3857053
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs3796661
rs3796661
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs3775423
rs3775423
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs356200
rs356200
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs356188
rs356188
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs2298728
rs2298728
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs2197120
rs2197120
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

dbSNP: rs2197120
rs2197120
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs10516845
rs10516845
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011

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
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: 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: 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
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
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: rs356220
rs356220
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.850 GeneticVariation GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012

dbSNP: rs356220
rs356220
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.850 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs356220
rs356220
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
T 0.850 GeneticVariation GWASDB SNCA_ rs356220 was associated with both Sporadic-PD (OR = 1.37, P = 1 × 10(-9)) and Familial-PD (OR = 1.40, P = 2 × 10(-5)). 24511991

2014

dbSNP: rs356220
rs356220
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
T 0.850 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010

dbSNP: rs356220
rs356220
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
A 0.850 GeneticVariation GWASDB Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. 21044948

2011

dbSNP: rs356220
rs356220
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
T 0.850 GeneticVariation GWASDB Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. 21084426

2011