rs356219
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.900 |
GeneticVariation |
GWASDB |
Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
|
24511991 |
2014 |
rs11931074
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.900 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs356219
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.900 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs356219
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.900 |
GeneticVariation |
GWASCAT |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs11931074
|
SNCA;LOC105377329
|
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 |
rs356219
|
SNCA;LOC105377329
|
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 |
rs356219
|
SNCA;LOC105377329
|
Parkinson Disease
|
G |
0.900 |
GeneticVariation |
GWASCAT |
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
|
21292315 |
2011 |
rs356219
|
SNCA;LOC105377329
|
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 |
rs11931074
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.900 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.
|
19915576 |
2009 |
rs11931074
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|
19915575 |
2009 |
rs11931074
|
SNCA;LOC105377329
|
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 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
|
0.860 |
GeneticVariation |
GWASDB |
Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
|
24511991 |
2014 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
|
0.860 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
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 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
|
0.860 |
GeneticVariation |
GWASDB |
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
|
20070850 |
2010 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
|
0.860 |
GeneticVariation |
GWASDB |
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
|
20711177 |
2010 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
|
0.860 |
GeneticVariation |
GWASCAT |
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
|
20070850 |
2010 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
C |
0.860 |
GeneticVariation |
GWASCAT |
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|
19915575 |
2009 |
rs2736990
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Parkinson Disease
|
C |
0.860 |
GeneticVariation |
GWASDB |
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|
19915575 |
2009 |
rs104893875
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Lewy Body Disease
|
|
0.860 |
GeneticVariation |
UNIPROT |
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.
|
14755719 |
2004 |
rs104893875
|
Entrez Id: |
6622 |
Gene Symbol: |
SNCA |
SNCA
|
Lewy Body Disease
|
T |
0.860 |
CausalMutation |
CLINVAR |
|
|
|
rs356220
|
SNCA;LOC105377329
|
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 |
rs356220
|
SNCA;LOC105377329
|
Parkinson Disease
|
T |
0.850 |
GeneticVariation |
GWASCAT |
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 |
rs356220
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.850 |
GeneticVariation |
GWASCAT |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
|
22451204 |
2012 |
rs356220
|
SNCA;LOC105377329
|
Parkinson Disease
|
|
0.850 |
GeneticVariation |
GWASDB |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
|
22451204 |
2012 |