rs8070723
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
|
24842889 |
2014 |
rs8070723
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs8070723
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
|
21738487 |
2011 |
rs8070723
|
|
|
0.800 |
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 |
rs8070723
|
|
|
0.800 |
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 |
rs8070723
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|
19915575 |
2009 |
rs62063857
|
|
|
0.730 |
GeneticVariation |
BEFREE |
The four previously reported Parkinson's disease (PD)-related single-nucleotide polymorphisms (SNPs) - rs1775143, rs823114, rs2071746 and rs62063857 - have rarely been studied in Chinese Han populations.
|
28535700 |
2017 |
rs62063857
|
|
|
0.730 |
GeneticVariation |
BEFREE |
Consequently, the rs62063857 polymorphism of the saitohin gene is a genetic risk factor for Parkinson's disease.
|
25168738 |
2015 |
rs1052553
|
|
|
0.730 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs62063857
|
|
|
0.730 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs1052553
|
|
|
0.730 |
GeneticVariation |
BEFREE |
All 4 SNCA SNPs and the MAPT H1-haplotype-defining SNP (rs1052553) displayed a highly significant marginal association with PD at the significance level adjusted for multiple comparisons.
|
21391235 |
2011 |
rs1052553
|
|
|
0.730 |
GeneticVariation |
BEFREE |
Our findings indicate that as previously reported, the SNCA rs356219-G allele and MAPT rs1052553 (H1 haplotype) were both associated with an increased risk of PD, whilst contrary to previous reports, GSK3B variants were not.
|
21159074 |
2011 |
rs1052553
|
|
|
0.730 |
GeneticVariation |
BEFREE |
We identified a significant association between H1/H2 and risk of PD (rs1052553 OR: 1.43, CI: 1.23-1.64; rs62063857 OR: 1.45, CI: 1.27-1.67), but no effect of the H1-specific SNP rs242557 (OR: 0.92, CI: 0.82-1.03).
|
19912324 |
2010 |
rs62063857
|
|
|
0.730 |
GeneticVariation |
BEFREE |
We identified a significant association between H1/H2 and risk of PD (rs1052553 OR: 1.43, CI: 1.23-1.64; rs62063857 OR: 1.45, CI: 1.27-1.67), but no effect of the H1-specific SNP rs242557 (OR: 0.92, CI: 0.82-1.03).
|
19912324 |
2010 |
rs17649553
|
|
|
0.720 |
GeneticVariation |
BEFREE |
Five out of the 13 tested SNPs (rs12185268, rs6599389, rs356220, rs13312, and rs17649553) were confirmed to be nominally significantly associated (<i>P</i> < 0.05) with PD risk in the Cypriot population.
|
31681140 |
2019 |
rs17649553
|
|
C |
0.720 |
GeneticVariation |
GWASCAT |
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
|
28892059 |
2017 |
rs17649553
|
|
|
0.720 |
GeneticVariation |
BEFREE |
Here, in order to discover potential AD-related loci, we investigated the association between late-onset AD (LOAD) susceptibility and nine single-nucleotide polymorphisms (SNPs) (rs11724635 of BST1, rs12637471 of MCCC1, rs15553999 of TMEM229, rs17649553 of MAPT, rs34311866 of TMEM175-GAK-DGKQ, rs356182 of SNCA, rs6430538 of ACMSD-TMEM163, rs76904798 of LRRK2 and rs823118 of RAB7L1-NUCKS1) which were reported to have genome-wide significant associations with PD risk in a recent Genome Wide Association Study performed among white population.
|
26738859 |
2017 |
rs17649553
|
|
C |
0.720 |
GeneticVariation |
GWASCAT |
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
|
25064009 |
2014 |
rs1800547
|
|
|
0.720 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs1800547
|
|
|
0.720 |
GeneticVariation |
BEFREE |
Single-nucleotide polymorphisms in MAPT (rs1800547; P = 3.1 × 10(-4) ) and SNCA (rs356219; P = 5.5 × 10(-4) ) were significantly associated with Parkinson's disease.
|
21425343 |
2011 |
rs1800547
|
|
|
0.720 |
GeneticVariation |
GWASDB |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
|
21738487 |
2011 |
rs1800547
|
|
|
0.720 |
GeneticVariation |
BEFREE |
After adjusting for multiple comparisons, SNP rs1800547 was significantly associated with PD affection.
|
18509094 |
2008 |
rs17563986
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
|
24842889 |
2014 |
rs10445337
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |
rs10445338
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|
22438815 |
2012 |