Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs823156
rs823156
0.850 GeneticVariation BEFREE SNPs rs11240569, rs708727, and rs823156 in <i>SLC41A1</i> Do Not Discriminate Between Slovak Patients with Idiopathic Parkinson's Disease and Healthy Controls: Statistics and Machine-Learning Evidence. 31546642

2019

dbSNP: rs823156
rs823156
0.850 GeneticVariation BEFREE Through meta-analysis, we confirmed that minor variants of rs823128A>G, rs1572931C>T, and rs823156A>G played protective roles in PD. 28749816

2017

dbSNP: rs823156
rs823156
0.850 GeneticVariation BEFREE Through bioinformatic analysis, we predicted that rs823128, rs1572931, and rs823156 as noncoding variants of NUCKS1, RAB29, and SLC41A1, respectively, might affect PD risk by altering the transcription factor-binding capability of the genes. 28749816

2017

dbSNP: rs823156
rs823156
0.850 GeneticVariation BEFREE The PARK16 SNPs rs823128, rs947211, and rs823156 and the CAAAC, TGAGA, and CAGAC haplotypes may be significantly associated with sporadic PD in Japan. 26944116

2016

dbSNP: rs823156
rs823156
0.850 GeneticVariation BEFREE The associations between rs823128/rs823156/rs708730 and PD are more likely to be replicated in Chinese and Malay populations. 25758099

2015

dbSNP: rs823156
rs823156
0.850 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815

2012

dbSNP: rs823156
rs823156
A 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: rs823156
rs823156
A 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: rs823156
rs823156
0.850 GeneticVariation BEFREE Genome-wide association studies (GWAS) have identified several single-nucleotide polymorphisms (SNPs) at the PARK16 locus that can modulate the risk of Parkinson's disease (PD), including rs16856139, rs823128, rs823122, rs947211, rs823156, rs708730 and rs11240572. 21840748

2011