Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12490683
rs12490683
0.010 GeneticVariation BEFREE Genotyping studies identified two MYLKP1 SNPs (rs12490683; rs12497343) that significantly increase risk of colon cancer in African Americans compared to African American controls. 30161129

2018

dbSNP: rs12497343
rs12497343
0.010 GeneticVariation BEFREE Genotyping studies identified two MYLKP1 SNPs (rs12490683; rs12497343) that significantly increase risk of colon cancer in African Americans compared to African American controls. 30161129

2018

dbSNP: rs12778366
rs12778366
0.010 GeneticVariation BEFREE Sex- and subsite-specific Cox hazard ratios (HRs) showed that the rs12778366 CC versus TT genotype decreased CRC and colon cancer risks in women (HR<sub>CRC</sub> = 0.53, 95% confidence interval: 0.30-0.94) but not men. 30410074

2018

dbSNP: rs1383147053
rs1383147053
DLD
0.010 GeneticVariation BEFREE We examined the anti-proliferative effect of miR-143#12 and the mechanism in human colon cancer DLD-1 cell (G13D) and other cell types harboring K-Ras mutations. 29498789

2018

dbSNP: rs147740818
rs147740818
0.010 GeneticVariation BEFREE Colon cancers carrying BRAF V600E and β-catenin T41A activating mutations are resistant to numerous common anticancer drugs. 29541216

2018

dbSNP: rs16840252
rs16840252
0.010 GeneticVariation BEFREE In addition, we found the CTLA-4 rs16840252 C>T polymorphism was associated with the risk of colon cancer. 30122952

2018

dbSNP: rs1799853
rs1799853
0.010 GeneticVariation BEFREE Site-specific analysis showed association between SNPs rs1799853 and rs2302615 with reduced colon cancer risk only (P = 0.01 and P = 0.004, respectively), however neither reached significance threshold following multiple test correction. 29425227

2018

dbSNP: rs2302615
rs2302615
0.010 GeneticVariation BEFREE Site-specific analysis showed association between SNPs rs1799853 and rs2302615 with reduced colon cancer risk only (P = 0.01 and P = 0.004, respectively), however neither reached significance threshold following multiple test correction. 29425227

2018

dbSNP: rs283415
rs283415
0.010 GeneticVariation BEFREE In female drinkers, ADH1C rs283415 increased proximal colon cancer risk. 29390059

2018

dbSNP: rs3804100
rs3804100
0.010 GeneticVariation BEFREE Real-time PCR and immunohistochemistry were used to investigate <i>TLR2</i> gene expression and to evaluate the potential risk of predisposition to colon cancer caused by three tagging single-nucleotide polymorphisms (SNPs) on <i>TLR2</i>, including rs3804100, rs4696480, and rs3804099. 30532554

2018

dbSNP: rs3811802
rs3811802
0.010 GeneticVariation BEFREE ADH1B rs3811802 and ADH1C rs4147542 significantly modified the alcohol-colon cancer association in women. 29390059

2018

dbSNP: rs4147536
rs4147536
0.010 GeneticVariation BEFREE In male drinkers, ADH1B rs4147536 increased (distal) colon cancer risk. 29390059

2018

dbSNP: rs4147542
rs4147542
0.010 GeneticVariation BEFREE ADH1B rs3811802 and ADH1C rs4147542 significantly modified the alcohol-colon cancer association in women. 29390059

2018

dbSNP: rs4696480
rs4696480
0.010 GeneticVariation BEFREE Thus, <i>TLR2</i> rs4696480 appear to be not involved in colon cancer in our study population. 30532554

2018

dbSNP: rs730881834
rs730881834
0.010 GeneticVariation BEFREE We report a MUTYH variant, p.C306W (c.918C>G), with a tryptophan residue in place of native cysteine, that ligates the [4Fe4S] cluster in a patient with colonic polyposis and family history of early age colon cancer. 29915346

2018

dbSNP: rs752021744
rs752021744
0.010 GeneticVariation BEFREE We examined the anti-proliferative effect of miR-143#12 and the mechanism in human colon cancer DLD-1 cell (G13D) and other cell types harboring K-Ras mutations. 29498789

2018

dbSNP: rs773442580
rs773442580
EGF
0.010 GeneticVariation BEFREE Furthermore, EGF‑ETA was just as potent in HCT116 (KRAS G13D) and SW480 (KRAS G12V) colon cancer cell lines harbouring KRAS hyperactivating mutations when compared to KRAS wild‑type HT29 colon cancer cells. 30226622

2018

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: 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: rs17250717
rs17250717
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: rs1799929
rs1799929
0.010 GeneticVariation BEFREE High fried red meat intake associated with NAT2-T341C, G590A, G857A, A845C, and C48</span>1T rapid acetylator allele determines a risk of 2.39 (P=.002), 2.39 (P=.002), 2.37 (P=.002), 2.28 (P=.004), and 2.51 (P=.001), respectively, for colon cancer, whereas in the case of rectal cancer, the risk increased to 7.55 (P<.001), 7.7 (P<.001), 7.83 (P<.001), 7.51 (P<.001), and 8.62 (P<.001), respectively. 27883249

2017

dbSNP: rs1800734
rs1800734
0.010 GeneticVariation BEFREE Our aim was to determine the effect of the single nucleotide polymorphisms (SNP) -93G>A of the MLH1 gene (rs1800734) and Gly322Asp of the MSH2 gene (rs4987188) on the risk of colon cancer (CC) and identify any relationship with clinical factors. 29181059

2017

dbSNP: rs1801133
rs1801133
0.010 GeneticVariation BEFREE However, <i>MTHFR</i> rs1801133 G>A polymorphism conferred a decreased risk to colon cancer. 28969008

2017

dbSNP: rs1801725
rs1801725
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: rs1802757
rs1802757
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