Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12646351
rs12646351
0.700 GeneticVariation GWASCAT Genome wide association study to identify predictors for severe skin toxicity in colorectal cancer patients treated with cetuximab. 30557370

2018

dbSNP: rs17806780
rs17806780
0.700 GeneticVariation GWASCAT Genome wide association study to identify predictors for severe skin toxicity in colorectal cancer patients treated with cetuximab. 30557370

2018

dbSNP: rs704017
rs704017
G 0.700 GeneticVariation GWASCAT Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. 24836286

2014

dbSNP: rs704017
rs704017
G 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142

2019

dbSNP: rs704017
rs704017
G 0.700 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119

2019

dbSNP: rs704017
rs704017
G 0.700 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

2019

dbSNP: rs704017
rs704017
G 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs704017
rs704017
G 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016

dbSNP: rs1250567
rs1250567
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs10511330
rs10511330
C 0.700 GeneticVariation GWASCAT Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. 29942513

2018

dbSNP: rs1912804
rs1912804
0.700 GeneticVariation GWASCAT Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. 29228715

2017

dbSNP: rs10506868
rs10506868
T 0.700 GeneticVariation GWASCAT Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. 26965516

2016

dbSNP: rs12241008
rs12241008
C 0.700 GeneticVariation GWASCAT GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12. 29471430

2018

dbSNP: rs12241008
rs12241008
C 0.700 GeneticVariation GWASCAT Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. 25105248

2014

dbSNP: rs12241008
rs12241008
C 0.700 GeneticVariation GWASCAT Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. 30529582

2019

dbSNP: rs12246635
rs12246635
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs12255141
rs12255141
G 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142

2019

dbSNP: rs117079142
rs117079142
A 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs76316943
rs76316943
A 0.700 GeneticVariation GWASCAT A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. 25990418

2015

dbSNP: rs11168936
rs11168936
C 0.700 GeneticVariation GWASCAT Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. 27197191

2016

dbSNP: rs12143541
rs12143541
G 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142

2019

dbSNP: rs12144319
rs12144319
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs2186607
rs2186607
T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241

2019

dbSNP: rs1131691039
rs1131691039
A 0.700 GeneticVariation CLINVAR

dbSNP: rs11540652
rs11540652
T 0.700 CausalMutation CLINVAR