Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASDB Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286

2014

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation GWASDB Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556

2013

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASDB Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. 18372901

2008

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASDB Across the four sample sets, the association between rs4939827 and CRC was highly statistically significant (P(trend) = 1.0 x 10(-12)). 17934461

2007

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation GWASDB Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. 19011631

2008

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation GWASDB Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138

2012

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASCAT Across the four sample sets, the association between rs4939827 and CRC was highly statistically significant (P(trend) = 1.0 x 10(-12)). 17934461

2007

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

2019

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821

2015

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119

2019

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556

2013

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138

2012

dbSNP: rs4939827
rs4939827
T 0.900 GeneticVariation GWASCAT Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. 18372901

2008

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE In the end, we identified the T allele of rs4939827 to be significantly related with an increase CRC risk (P=2.22E-05, OR=1.14, 95% CI 1.07-1.21) in Chinese population. 28467803

2017

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE In conclusion, our data suggest that SMAD7 rs4939827 and CHI3L1 rs4950928 SNPs have no significant association with CRC. 26779637

2016

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Results from our case-control study and the meta-analysis collectively confirmed the significant association of the variant rs4939827 with increased risk of colorectal cancer. 22457752

2012

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE A decreased risk for CRC cancer was observed for the CC compared to the TT genotype (OR = 0.65 and 95% CI = 0.51-0.81) of the rs4939827 SNP Also, we could show an association between the Mediterranean diet pattern (protective factor) and rs4939827. 29084532

2017

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Our results show association of rs4939827 with colorectal cancer</span> risk in Croatian population. 24066093

2013

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Two recent genome-wide association studies (GWAS) identified three common variants in SMAD7 (rs4464148, rs4939827 and rs12953717) that confer modest susceptibility to colorectal cancer. 19357349

2009

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE We confirmed the association of CRC risk with four SNPs, with odds ratio (OR) higher than previously reported: rs16892766 on 8q23.3 (OR: 1.88, 95% confidence interval (CI): 1.30-2.72; P=0.0007); rs4779584 on 15q13.3 (OR: 1.42, CI: 1.11-1.83; P=0.0061) and rs4939827 and rs58920878/Novel 1 on 18q21.1 (OR: 1.49, CI: 1.13-1.98; P=0.007 and OR: 1.49, CI: 1.14-1.95; P=0.0035). 25873010

2016

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Subgroup analysis according to ethnicity showed rs4464148 and rs12953717 were associated with the risk of CRC in both Caucasians and Asians, whereas rs4939827 was a risk polymorphism for CRC specifically in Caucasians. 28070019

2016

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Among those with CRC, the minor allele (G) in rs4939827 was significantly associated with poorer overall survival (hazards ratio, 1.20; 95% CI, 1.02-1.42). 23104301

2013

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Two previous genome-wide association studies identified three single nucleotide polymorphisms (SNPs) (rs4939827, rs12953717 and rs4464148) in SMAD7 to be associated with colorectal cancer in a Western population. 21221812

2011

dbSNP: rs4939827
rs4939827
0.900 GeneticVariation BEFREE Moreover, we found cumulative effects of three genetic factors (rs7758229, rs6983267, and rs4939827 in SMAD7) and one environmental factor (alcohol drinking) which appear to increase CRC risk approximately twofold. 21242260

2011