Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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 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
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 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 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 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 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 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: rs3818361
rs3818361
CR1
0.880 GeneticVariation BEFREE The aim of this study was to examine whether the variants of some candidate genes involved in the development of AD, namely BIN1 (rs744373), CLU (rs11136000), CR1 (rs3818361), and PICALM (rs3851179), are related to several disorders of glucose metabolism-gestational diabetes (GDM), T2DM and impaired glucose tolerance (IGT). 28316001

2017

dbSNP: rs3818361
rs3818361
CR1
0.880 GeneticVariation BEFREE In summary, this is the first study to show significan</span></span>t association between rs3818361 polymorphism and AD in Chinese population by a meta-analysis method. 26189835

2016

dbSNP: rs3818361
rs3818361
CR1
0.880 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: rs3818361
rs3818361
CR1
0.880 GeneticVariation BEFREE We also independently replicate our observation of lower brain amyloid burden in risk allele carriers of rs3818361 in the Alzheimer's Disease Neuroimaging Initiative sample. 23022416

2013

dbSNP: rs3818361
rs3818361
CR1
0.880 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: rs3818361
rs3818361
CR1
0.880 GeneticVariation BEFREE Meta-analysis of available studies (n = 31,771 individuals), including previous studies and public genome-wide association study resources (Alzheimer's Disease Neuroimaging Initiative, Translational Genomics Research Institute, and Multi-site Collaborative Study for Genotype-Phenotype Associations in Alzheimer's Disease), strongly supports the effect of rs3818361 (odds ratio = 1.180, 95% confidence interval: 1.113-1.252, P < 2.99E-8) and suggests the existence of between-study heterogeneity (P < .05). 21784344

2011

dbSNP: rs3818361
rs3818361
CR1
0.880 GeneticVariation BEFREE The results revealed that there were significant differences in genotype (P=0.02) and allele (P=0.007) frequencies of the SNP rs6656401 but no in rs3818361 between AD patients and controls. 20558149

2010

dbSNP: rs3818361
rs3818361
CR1
0.880 GeneticVariation BEFREE Unadjusted, CLU (odds ratio [OR], 0.91; 95% confidence interval [CI], 0.85-0.96 for single-nucleotide polymorphism [SNP] rs11136000), CR1 (OR, 1.14; 95% CI, 1.07-1.22; SNP rs3818361), and PICALM (OR, 0.89; 95% CI, 0.84-0.94, SNP rs3851179) were associated with AD in white individuals. 20697030

2010

dbSNP: rs6701713
rs6701713
CR1
0.810 GeneticVariation BEFREE In this case-control study, we aimed to investigate whether single nucleotide polymorphisms in MTHFR (rs1801133), PICALM (3851719), CLU (rs11136000), and CR1 (rs6701713) are associated with AD. 25359311

2015

dbSNP: rs4844610
rs4844610
CR1
0.710 GeneticVariation BEFREE Individuals with F/S genotype had a 1.8 times increased risk for AD compared with F/F genotype (p-adjusted = 0.003), while rs4844610 was only marginally significant (p-adjusted = 0.024). 22819390

2012

dbSNP: rs1344800847
rs1344800847
CR1
0.010 GeneticVariation BEFREE In AD patients carrying the H allele (<i>Hin</i>dIII polymorphism) or the Q allele (Q981H polymorphism), CR1/E was significantly lower when compared with controls carrying the same alleles (<i>p</i> < 0.01), contrary to sCR1, which was significantly higher (<i>p</i> < 0.001). 30044434

2018

dbSNP: rs3738467
rs3738467
CR1
0.010 GeneticVariation BEFREE In AD patients carrying the H allele (<i>Hin</i>dIII polymorphism) or the Q allele (Q981H polymorphism), CR1/E was significantly lower when compared with controls carrying the same alleles (<i>p</i> < 0.01), contrary to sCR1, which was significantly higher (<i>p</i> < 0.001). 30044434

2018

dbSNP: rs4844609
rs4844609
CR1
0.010 GeneticVariation BEFREE The Ser1610Thr variant was not associated with AD</span>, memory impairment, total tau, amyloid β(1-42) or tau phosphorylated at threonine 181 levels. 23582656

2013