Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation GWASDB Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556

2013

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation GWASDB Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. 19011631

2008

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation BEFREE An association between SNP rs3802842 on chromosome 11q23.1 and rs16892766 on chromosome 8q23.3 and the risk of developing CRC and age of diagnosis was found in MLH1 mutation carriers. 21097774

2011

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation BEFREE Collectively, our analysis further supports previous findings that the rs16892766</span> polymorphism is significantly associated with CRC susceptibility. 25609216

2015

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation BEFREE In addition to the previously reported 8q24, 15q13 and 18q21 CRC risk loci, we identified two previously unreported associations: rs10795668, located at 10p14 (P = 2.5 x 10(-13) overall; P = 6.9 x 10(-12) replication), and rs16892766, at 8q23.3 (P = 3.3 x 10(-18) overall; P = 9.6 x 10(-17) replication), which tags a plausible causative gene, EIF3H. 18372905

2008

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation BEFREE Our findings demonstrated that rs16892766-C allele might be risk-conferring factors for the development of CRC, but not for CRA. 25293934

2015

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation GWASDB Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population. 22532847

2012

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821

2015

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation BEFREE The aim of this study was to perform an association study between risk variants: rs10795668, rs16892766, rs3802842 and rs4939827 and CRC risk in Croatian population. 24066093

2013

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119

2019

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 GeneticVariation BEFREE Overall, the association of most CRC susceptibility loci identified in initial GWAS seems to be invariant to the other risk factors considered; however, our results suggest potential modification of the rs16892766 effect by vegetable consumption. 22367214

2012

dbSNP: rs16892766
rs16892766
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
A 0.900 GeneticVariation GWASCAT In addition to the previously reported 8q24, 15q13 and 18q21 CRC risk loci, we identified two previously unreported associations: rs10795668, located at 10p14 (P = 2.5 x 10(-13) overall; P = 6.9 x 10(-12) replication), and rs16892766, at 8q23.3 (P = 3.3 x 10(-18) overall; P = 9.6 x 10(-17) replication), which tags a plausible causative gene, EIF3H. 18372905

2008

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation BEFREE We used meta-analysis of an efficient empirical-Bayes estimator to detect potential multiplicative interactions between each of the SNPs [rs16892766 at 8q23.3 (EIF3H/UTP23), rs6983267 at 8q24 (MYC), rs10795668 at 10p14 (FLJ3802842), rs3802842 at 11q23 (LOC120376), rs4444235 at 14q22.2 (BMP4), rs4779584 at 15q13 (GREM1), rs9929218 at 16q22.1 (CDH1), rs4939827 at 18q21 (SMAD7), rs10411210 at 19q13.1 (RHPN2), and rs961253 at 20p12.3 (BMP2)] and select major CRC risk factors (sex, body mass index, height, smoking status, aspirin/nonsteroidal anti-inflammatory drug use, alcohol use, and dietary intake of calcium, folate, red meat, processed meat, vegetables, fruit, and fiber). 22367214

2012

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation BEFREE This meta-analysis demonstrated that the rs4779584 and rs10318 polymorphism at 15q13.3 is a risk factor associated with increased CRC/CRA susceptibility, but these associations vary in different ethnic populations. 25475391

2015

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation GWASCAT A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. 18372905

2008

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation GWASCAT Meta-analysis of new genome-wide association studies of colorectal cancer risk. 21761138

2012

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation BEFREE GREM1-SCG5 rs4779584 polymorphisms may increase the risk of developing colorectal cancer. 24586997

2014

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
T 0.870 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821

2015

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 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: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation BEFREE In a large series of colorectal cancer cases and controls, SNPs near GREM1 and SCG5 were strongly associated with increased CRC risk (for rs4779584, P = 4.44 x 10(-14)). 18084292

2008

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation BEFREE Near GREM1, we found using fine-mapping that the previously-identified association between tagSNP rs4779584 and CRC actually resulted from two independent signals represented by rs16969681 (P = 5.33×10(-8)) and rs11632715 (P = 2.30×10(-10)). 21655089

2011

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation GWASDB Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556

2013

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation GWASDB A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. 18372905

2008

dbSNP: rs4779584
rs4779584
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 GeneticVariation GWASDB Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. 19011631

2008