Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation GWASCAT Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. 30805717

2019

dbSNP: rs6656401
rs6656401
CR1
A 0.900 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. 30617256

2019

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation GWASCAT Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. 31473137

2019

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Three genotypes significantly associated with reduced AD risk relative to PART in the PENN (<i>N</i> = 377) and NACC (<i>N</i> = 1189) cohorts including <i>APOE ε</i>4, <i>APOE ε</i>2, and rs6656401 in the <i>CR1</i> gene. 30128317

2018

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Altogether, five loci (rs6656401 at CR1, rs983392within MS4A6A, rs11218343 at SORL1, rs6733839 at BIN1, and APOE ε4) have been detected to be associated with one or a few established AD-related neuroimaging measures. 26732597

2017

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Our analysis further supports previous findings that the CR1 rs6656401 polymorphism contributes to AD susceptibility. 24878768

2015

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Our prevalent case study comparing prevalent AD cases (n = 428) with participants with no cognitive impairment (n = 524) revealed a significant association of rs6656401 and rs3818361 (CR1), rs2075650 (TOMM40), rs7561528 (BIN1), and rs3865444 (CD33) with late-onset AD that were robust to adjustment with age and apolipoprotein E ε4 genotype. 24176626

2014

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE It did not explain (part of) the association of genome wide association top single-nucleotide polymorphisms rs3818361/rs6656401, nor of the CR1 CNV, with AD in our cohort, whereas the CR1 CNV and rs3818361/rs6656401 represented the same association signal. 23582656

2013

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE We investigated the influence of the rs6656401 single nucleotide polymorphisms (SNP) of the CR1 gene, the rs3851179 SNP of the PICALM gene, and the rs11136000 SNP of the CLU gene on risk of AD in a Polish population. 23650005

2013

dbSNP: rs6656401
rs6656401
CR1
A 0.900 GeneticVariation GWASDB Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. 24162737

2013

dbSNP: rs6656401
rs6656401
CR1
A 0.900 GeneticVariation GWASCAT Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. 24162737

2013

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Using 1709 subjects (697 deceased) from the Religious Orders Study and the Rush Memory and Aging Project, we tested 41 single-nucleotide polymorphisms (SNPs) within the linkage disequilibrium block containing the published CR1 AD SNP (rs6656401) for associations with episodic memory decline, and then examined the functional consequences of the top result. 22343410

2012

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Here, we show that two Alzheimer's disease-associated CR1 variants, rs6656401 and rs3818361, are associated with major recurrent depression in females in a population-based cohort using individuals from the Generation Scotland: Scottish Family Health Study. 22244847

2012

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Accumulated evidence suggests that a variant within the CR1 gene (single nucleotide polymorphism rs6656401), known to increase risk for Alzheimer disease (AD), influences β-amyloid (Aβ) deposition in brain tissue. 22262751

2012

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE Gene-brain structure associations of 3 recently discovered risk genes for Alzheimer's disease, CLU (rs11136000C>T), CR1 (rs6656401G>A), and PICALM (rs3851179G>A), were investigated in 2 independent cohorts of young healthy adults (n = 430 and n = 492, respectively). 21726919

2011

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation GWASDB Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. 21460841

2011

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation BEFREE A recent large genome-wide association study (GWAS) has identified significant association of two single nucleotide polymorphisms (SNPs) (rs6656401 and rs3818361) in the CR1 gene with AD in Caucasians. 20558149

2010

dbSNP: rs6656401
rs6656401
CR1
0.900 GeneticVariation GWASDB Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. 19734903

2009

dbSNP: rs6656401
rs6656401
CR1
A 0.900 GeneticVariation GWASCAT Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. 19734903

2009