Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
rs356220
0.850 GeneticVariation GWASCAT Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204

2012

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

2012

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

2012

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

dbSNP: rs356220
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

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

2010

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

2010