Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs947211
rs947211
0.840 GeneticVariation BEFREE Therefore, our meta-analysis sug</span>gested that rs947211 variants (A allele, AG and GG genotypes) may decrease the risk of PD in overall population, particularly in Northeast Asian population; and T allele, TC and TT genotypes of rs1572913 variants contributed to decrease the risk of PD. 28807727

2017

dbSNP: rs947211
rs947211
0.840 GeneticVariation BEFREE Compared with the AA genotype of SNP rs947211, both the AG genotype and the GG genotype were significantly related to an increased risk of sporadic PD. 26944116

2016

dbSNP: rs947211
rs947211
0.840 GeneticVariation BEFREE Our study suggests a higher chance to detect the association between rs947211 and PD in Chinese, Malay, and other Caucasian groups because of the similar linkage disequilibrium pattern around rs947211. 25758099

2015

dbSNP: rs947211
rs947211
0.840 GeneticVariation BEFREE Our results show that minor allele frequencies of rs11248051 (odds ratio [OR] 1.522; p=0.016) and rs3129882 (OR 1.294; p=0.03), but not rs823128 and rs947211, were associated with risk for PD. 24373818

2014

dbSNP: rs947211
rs947211
0.840 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs947211
rs947211
0.840 GeneticVariation GWASCAT Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576

2009

dbSNP: rs947211
rs947211
A 0.840 GeneticVariation GWASDB Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576

2009