Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1017621656
rs1017621656
0.010 GeneticVariation BEFREE We now show that stable expression of oncogenic Ki-ras(G12V) c</span>onverts the HD6-4 colon cancer cell line from insensitive to TGF-beta1 to growth-promoted by TGF-beta1. 11029459

2001

dbSNP: rs10222633
rs10222633
0.010 GeneticVariation BEFREE Haplotype analysis within linkage blocks of CASR revealed the G-G-G-G-G-A-C haplotype (rs10222633-rs10934578-rs3804592-rs17250717-A986S-R990G-rs1802757) to be associated with a decreased OS of colon cancer (HR, 3.15; 95% CI, 1.66-5.96). 28765616

2017

dbSNP: rs1039659576
rs1039659576
MTR
0.010 GeneticVariation BEFREE Neither MTR D919G nor RFC 80G>A polymorphisms were associated with altered colon cancer risk. 16284371

2005

dbSNP: rs10411210
rs10411210
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

dbSNP: rs1042522
rs1042522
0.010 GeneticVariation BEFREE PIA identified SNPs that may interact with the GSTT1 polymorphism, including coding polymorphisms in TP53 (Arg72Pro in p53) and CASP8 (Asp302His in caspase 8), which may modify the association between this polymorphism and colon cancer. 16217767

2006

dbSNP: rs1042636
rs1042636
0.010 GeneticVariation BEFREE Haplotype analysis within linkage blocks of CASR revealed the G-G-G-G-G-A-C haplotype (rs10222633-rs10934578-rs3804592-rs17250717-A986S-R990G-rs1802757) to be associated with a decreased OS of colon cancer (HR, 3.15; 95% CI, 1.66-5.96). 28765616

2017

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: rs1042821
rs1042821
0.020 GeneticVariation BEFREE In microsatellite stable tumors, homozygous carriers of the G39E polymorphism had an increased risk of CIMP+ colon cancer (odds ratio (OR) 2.2, 95% confidence interval (CI) 1.1, 4.2) and BRAF V600E mutation (OR 3.1, 95% CI 1.01, 9.7) in a case-control comparison. 19582761

2009

dbSNP: rs1044129
rs1044129
0.010 GeneticVariation BEFREE Among seven target variants, rs1044129 at the miR-367 binding site of calcium channel ryanodine receptor gene 3 (RYR3) was associated with relapse-free survival (RFS) for colon cancer patients as a recessive model in a univariate analysis. 23393343

2013

dbSNP: rs10450310
rs10450310
0.010 GeneticVariation BEFREE Four SNPs in the 3'-untranslated region (UTR) of the gene (rs10082466, rs2120132, rs2099902, and rs10450310) were associated with an increased risk of colon cancer in African Americans. 22282660

2012

dbSNP: rs1045485
rs1045485
0.010 GeneticVariation BEFREE PIA identified SNPs that may interact with the GSTT1 polymorphism, including coding polymorphisms in TP53 (Arg72Pro in p53) and CASP8 (Asp302His in caspase 8), which may modify the association between this polymorphism and colon cancer. 16217767

2006

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE MDR1 C3435T polymorphism influences the development of colon cancer and adult acute myeloid leukemia by the association with transporting carcinogen. 18644389

2008

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE Genetic testing for C3435T MDR1 gene polymorphism may be a suitable test to evaluate the risk for colon cancer in patients under 50 years of age. 15912392

2005

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE The present study suggests that MDR1 2677G>T and 3435C>T polymorphism is not a risk factor for sporadic colon cancer among Bulgarians and that somatic mutation at these sites is not involved in the genesis of colon tumors. 17674045

2008

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE G2677T and C3435T polymorphisms are not associated with colon cancer risk and prognosis in a selected patient population. 19192650

2009

dbSNP: rs1051753269
rs1051753269
0.010 GeneticVariation BEFREE Through biochemical and cellular pharmacologic studies, we have determined that cells harboring the colon cancer-derived G719S and G724S mutants are responsive to cetuximab therapy in vitro and found that the requirement for asymmetric dimerization of these mutant EGFR to promote cellular transformation may explain their greater inhibition by cetuximab than small-molecule kinase inhibitors. 24894453

2014

dbSNP: rs1052133
rs1052133
0.040 GeneticVariation BEFREE The association of the Ser326Cys polymorphism in the 8-oxoguanine glycosylase (OGG1) gene with a colon carcinoma and diabetes mellitus has been examined. 23368532

2013

dbSNP: rs1052133
rs1052133
0.040 GeneticVariation BEFREE In a study of 1,604 incident colon cancer cases and 1,969 matched population-based controls genotyped for BER variants OGG1 (S326C) and XRCC1 (R194W, R280H, and R399Q), we found no associations with colon cancer overall. 19959686

2009

dbSNP: rs1052133
rs1052133
0.040 GeneticVariation BEFREE These results suggest that the hOGG1 Ser326Cys polymorphism is probably not a major contributor to individual colon cancer susceptibility overall, but the Cys/Cys genotype may alter the impact of some environmental factors on colon cancer development. 12717837

2003

dbSNP: rs1052133
rs1052133
0.040 GeneticVariation BEFREE There was no significant association between OGG1 Ser326Cys polymorphism and CRC, but the homozygous Cys/Cys variant genotype was associated with an increased risk of colon cancer (p<0.05). 21899442

2012

dbSNP: rs1057519725
rs1057519725
0.010 GeneticVariation BEFREE Furthermore, we characterized KRAS A146V biologically using colon cancer cells. 30448735

2019

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

2019

dbSNP: rs1060503118
rs1060503118
0.010 GeneticVariation BEFREE From the Colon Cancer Family Registry, we identified 10 carriers who had both a MUTYH mutation (6 with c.1187G>A p.(Gly396Asp), 3 with c.821G>A p.(Arg274Gln), and 1 with c.536A>G p.(Tyr179Cys)) and a MMR gene mutation (3 in MLH1, 6 in MSH2, and 1 in PMS2), 375 carriers of a single (monoallelic) MUTYH mutation alone, and 469 carriers of a MMR gene mutation alone. 26202870

2015

dbSNP: rs10741657
rs10741657
0.010 GeneticVariation BEFREE In the present study, we investigated the association of three functional gene variants in GC (rs2282679 T>G), DHCR7 (rs12785878 G>T) and CYP2R1 (rs10741657 A>G) with time to recurrence (TTR) in patients with stages II and III colon cancer. 23793229

2013

dbSNP: rs10759932
rs10759932
0.010 GeneticVariation BEFREE In contrast, the rs2770150 is associated with colon cancer in women aged over 50 years and is closely linked with the decreased levels of female sex hormones during the post-menopausal period (OR = 0.188, CI: 0.074-0.48, P = <0.00084). rs10759932 and rs4986790 appear to have any association with colon cancer. 26771524

2016