Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE (1) When men and women were assessed together, the frequencies of the MTHFR C677T and A1298 genotypes or their alleles were not significantly different between controls and co</span>lon cancer or rectal cancer cases. 18712959

2009

dbSNP: rs67376798
rs67376798
0.010 GeneticVariation BEFREE 5-fluorouracil toxicity in the treatment of colon cancer associated with the genetic polymorphism 2846 A>G (rs67376798). 27122156

2017

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Colon carcinoma BRAF V600E HT29 cells exhibited poor response to radiation compared to BRAF wild-type COLO320 and HCT116 cells. 29663854

2018

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Colon carcinoma BRAF V600E HT29 cells exhibited poor response to radiation compared to BRAF wild-type COLO320 and HCT116 cells. 29663854

2018

dbSNP: rs1380087059
rs1380087059
APC
0.010 GeneticVariation BEFREE A636P is associated with early-onset colon cancer in Ashkenazi Jews. 12595050

2003

dbSNP: rs1418586322
rs1418586322
0.010 GeneticVariation BEFREE A636P is associated with early-onset colon cancer in Ashkenazi Jews. 12595050

2003

dbSNP: rs587781394
rs587781394
APC
0.010 GeneticVariation BEFREE A636P is associated with early-onset colon cancer in Ashkenazi Jews. 12595050

2003

dbSNP: rs63750875
rs63750875
0.010 GeneticVariation BEFREE A636P is associated with early-onset colon cancer in Ashkenazi Jews. 12595050

2003

dbSNP: rs1443465532
rs1443465532
0.010 GeneticVariation BEFREE P125A-endostatin also localised into tumour tissue to a higher degree than the native protein, and displayed greater inhibition of growth of colon cancer in athymic mice. 15083196

2004

dbSNP: rs760891242
rs760891242
XPC
0.010 GeneticVariation BEFREE P125A-endostatin also localised into tumour tissue to a higher degree than the native protein, and displayed greater inhibition of growth of colon cancer in athymic mice. 15083196

2004

dbSNP: rs2032582
rs2032582
0.010 GeneticVariation BEFREE G2677T and C3435T polymorphisms are not associated with colon cancer risk and prognosis in a selected patient population. 19192650

2009

dbSNP: rs779066883
rs779066883
0.010 GeneticVariation BEFREE S100P/RAGE signaling regulates microRNA-155 expression via AP-1 activation in colon cancer. 23693020

2013

dbSNP: rs35301225
rs35301225
0.010 GeneticVariation BEFREE rs35301225 in miR-34a was highly associated with a decreased risk of CRC in a Chinese population and might serve as a novel biomarker for colon cancer. 28293146

2017

dbSNP: rs187960998
rs187960998
0.010 GeneticVariation BEFREE rs187960998 in miR-211 was highly associated with a decreased risk of CC in the Chinese population by deregulating a tumor suppressive gene CHD5. 30655677

2019

dbSNP: rs1057519822
rs1057519822
0.010 GeneticVariation BEFREE V211D Mutation in MEK1 Causes Resistance to MEK Inhibitors in Colon Cancer. 31227518

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE A colon cancer cell line with RNF43-G659Vfs*41 and BRAF-V600E mutations was sensitive to activation of Wnt/β-catenin signaling. 31811196

2019

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE A colon cancer cell line with RNF43-G659Vfs*41 and BRAF-V600E mutations was sensitive to activation of Wnt/β-catenin signaling. 31811196

2019

dbSNP: rs1801394
rs1801394
0.020 GeneticVariation BEFREE A haplotype of A66G and A1298C polymorphisms, A/A, proved to be protective (OR=0.775; 95% CI=0.603-0.996; p=0.04), whereas haplotype A/G was a risk factor for colon cancer (OR=1.270; 95% CI=1.007-1.602; p=0.04). 21438757

2011

dbSNP: rs397507444
rs397507444
0.090 GeneticVariation BEFREE A haplotype of A66G and A1298C polymorphisms, A/A, proved to be protective (OR=0.775; 95% CI=0.603-0.996; p=0.04), whereas haplotype A/G was a risk factor for colon cancer (OR=1.270; 95% CI=1.007-1.602; p=0.04). 21438757

2011

dbSNP: rs121913314
rs121913314
SRC
0.010 GeneticVariation BEFREE A recent report suggested that the risk of colon cancer is higher for those who carry a C-->T transition mutation on codon 531 (Gln-531-->Amber-531) of src gene. 10704743

2000

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE A set of 668 stage II and III CC samples from the PETACC-3 (Pan-European Trails in Alimentary Tract Cancers) clinical trial were used to assess differential gene expression between c.1799T>A (p.V600E) BRAF mutant and non-BRAF, non-KRAS mutant cancers (double wild type) and to construct a gene expression-based classifier for detecting BRAF mutant samples with high sensitivity. 22393095

2012

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE A set of 668 stage II and III CC samples from the PETACC-3 (Pan-European Trails in Alimentary Tract Cancers) clinical trial were used to assess differential gene expression between c.1799T>A (p.V600E) BRAF mutant and non-BRAF, non-KRAS mutant cancers (double wild type) and to construct a gene expression-based classifier for detecting BRAF mutant samples with high sensitivity. 22393095

2012

dbSNP: rs4950928
rs4950928
0.010 GeneticVariation BEFREE A significant association of SNP in SMAD7 rs4939827 and CHI3L1 rs4950928 was revealed between the rectal cancer and colon cancer patients. 26779637

2016

dbSNP: rs1042821
rs1042821
0.020 GeneticVariation BEFREE A study was conducted to examine whether MLH1 (-93G>A and Ile219Val) and MSH6 (Gly39Glu) polymorphisms were associated with risk of colon cancer in data from 1609 colon cancer cases and 1972 controls. 18523027

2009

dbSNP: rs16892766
rs16892766
0.010 GeneticVariation BEFREE A total of 927 MMR gene mutation carriers (360 MLH1, 442 MSH2, 85 MSH6 and 40 PMS2) from 315 families enrolled in the Colon Cancer Family Registry, were genotyped for the single nucleotide polymorphisms (SNPs): rs16892766 (8q23.3), rs6983267 (8q24.21), rs719725 (9p24), rs10795668 (10p14), rs3802842 (11q23.1), rs4444235 (14q22.2), rs4779584 (15q13.3), rs9929218 (16q22.1), rs4939827 (18q21.1), rs10411210 (19q13.1) and rs961253 (20p12.3). 23434150

2013