rs356220
|
|
|
0.850 |
GeneticVariation |
BEFREE |
We provided further evidence that rs356220 is associated with increased risk of PD supporting previous studies in Caucasian-based and Japanese populations.
|
26732583 |
2016 |
rs356220
|
|
|
0.850 |
GeneticVariation |
BEFREE |
Our results show that rs2736990 and rs356220 in SNCA decreased the risk for PD in a Chinese population.
|
25129240 |
2014 |
rs356220
|
|
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
|
|
|
0.850 |
GeneticVariation |
BEFREE |
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
|
|
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
|
|
|
0.850 |
GeneticVariation |
BEFREE |
The additive interactions between SNPs rs356219 and rs356220 and smoking with respect to sporadic PD were significant although the multiplicative interactions were not significant.
|
22425546 |
2012 |
rs356220
|
|
|
0.850 |
GeneticVariation |
GWASCAT |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
|
22451204 |
2012 |
rs356220
|
|
|
0.850 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs356220
|
|
|
0.850 |
GeneticVariation |
GWASDB |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
|
22451204 |
2012 |
rs356220
|
|
|
0.850 |
GeneticVariation |
BEFREE |
Compared with subjects with the CC or CA genotype of UCHL1 S18Y and the CC or CT genotype of SNCA SNP rs356220, those with the AA genotype of UCHL1 S18Y and the TT genotype of SNP rs356220 had a significantly increased risk of sporadic PD; the interaction, however, was not significant.
|
22839974 |
2012 |
rs356220
|
|
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 |
rs356220
|
|
T |
0.850 |
GeneticVariation |
GWASDB |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
|
21738487 |
2011 |
rs356220
|
|
A |
0.850 |
GeneticVariation |
GWASCAT |
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
|
21044948 |
2011 |
rs356220
|
|
T |
0.850 |
GeneticVariation |
GWASCAT |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
|
21738487 |
2011 |
rs356220
|
|
T |
0.850 |
GeneticVariation |
GWASCAT |
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 |
rs356220
|
|
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 |
rs356220
|
|
T |
0.850 |
GeneticVariation |
GWASCAT |
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
|
20711177 |
2010 |
rs356220
|
|
T |
0.850 |
GeneticVariation |
GWASDB |
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
|
20711177 |
2010 |