Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs118049207
rs118049207
0.010 GeneticVariation BEFREE Stratification and interaction analyses showed that SND1 rs118049207</span> multiplicatively interacted with the sex and drinking status of the patients to enhance their colorectal cancer risk (P = 1.56×10-3 and 1.41×10-2, respectively). 31579913

2020

dbSNP: rs1267969615
rs1267969615
ACE
0.010 GeneticVariation BEFREE Our findings suggest that the angiotensin-converting enzyme I/D and angiotensinogen M235T polymorphisms are unlikely to correlate with colorectal cancer. 31642377

2020

dbSNP: rs2070804
rs2070804
0.010 GeneticVariation BEFREE We demonstrated the association of HSPB1 genetic polymorphisms rs2070804 with tumor depth with colorectal cancer. 31364192

2020

dbSNP: rs2279744
rs2279744
0.010 GeneticVariation BEFREE The polymorphism T309G (rs2279744) in the MDM2 gene was studied in patients with colorectal cancer (n=135) and healthy control subjects (n=145) using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method. 31424672

2020

dbSNP: rs2470151
rs2470151
0.010 GeneticVariation BEFREE These findings suggest that <i>RP11-108K3.2</i> rs2470151 had a significant association with the risk of colorectal cancer; this may help to predict the susceptibility of colorectal cancer in Chinese populations. 31789575

2020

dbSNP: rs2555639
rs2555639
0.010 GeneticVariation BEFREE Single nucleotide polymorphism rs2555639 in 15-PGDH and colorectal cancer metastasis. 31646799

2020

dbSNP: rs699
rs699
AGT
0.010 GeneticVariation BEFREE Our findings suggest that the angiotensin-converting enzyme I/D and angiotensinogen M235T polymorphisms are unlikely to correlate with colorectal cancer. 31642377

2020

dbSNP: rs1057519860
rs1057519860
0.010 GeneticVariation BEFREE Growth suppression of colorectal cancer expressing S492R EGFR by monoclonal antibody CH12. 30671888

2019

dbSNP: rs1063169
rs1063169
FOS
0.010 GeneticVariation BEFREE The rs7101 and rs1063169 polymorphisms in the noncoding region of FOS are associated with the risk of developing colorectal cancer and the progression of colorectal cancer, which may be because the mutation enhances the expression of c-Fos protein to promote the incidence and development of colorectal cancer. 31261535

2019

dbSNP: rs1064795841
rs1064795841
0.010 GeneticVariation BEFREE Association between KRAS G13D mutations and anastomotic recurrence in colorectal cancer: Two case reports. 30896620

2019

dbSNP: rs10889677
rs10889677
0.010 GeneticVariation BEFREE Single nucleotide polymorphism rs10889677 in miRNAs Let-7e and Let-7f binding site of IL23R gene is a strong colorectal cancer determinant: Report and meta-analysis. 31546198

2019

dbSNP: rs1282801317
rs1282801317
0.010 GeneticVariation BEFREE In the present study, two novel non-hotspot <i>KRAS</i> mutations were functionally characterized <i>in vitro</i>: KRAS E31D was identified from a genetic screen of colorectal cancer specimens at the UP-National Institutes of Health. 31289513

2019

dbSNP: rs13072632
rs13072632
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167

2019

dbSNP: rs1428
rs1428
0.010 GeneticVariation BEFREE Overall analysis found that rs7336610 and rs1428 and haplotype CTAGA were significantly associated with increased risk of colorectal cancer. 30941921

2019

dbSNP: rs1456315
rs1456315
0.010 GeneticVariation BEFREE The genotyping analysis for SNP rs1456315 showed increased association with colorectal cancer with the homozygous CC variant allele (OR: 2.09; χ2 = 4.95; CI: 1.08-4.02; p = 0.02), the minor allele frequency, and additive genotype, respectively (OR: 1.55; χ2 = 6.24; CI: 1.09-2.19; p = 0.01) & (OR: 1.64; χ2 = 4.04; CI: 1.01-2.67; p = 0.04). 31487296

2019

dbSNP: rs146639652
rs146639652
0.010 GeneticVariation BEFREE Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma. 30368636

2019

dbSNP: rs1590
rs1590
0.010 GeneticVariation BEFREE Based on these findings, the rs1590 variant in the 3'-UTR of TGFBR1 may contribute to the susceptibility to colorectal cancer, predominantly by altering miR-532-5p binding. 29971498

2019

dbSNP: rs16917496
rs16917496
0.010 GeneticVariation BEFREE The rs16917496 polymorphism including CC, CT and TT genotypes was analyzed in patients with colorectal cancer; the CC genotype was identified to be independently associated with longer post-operative survival times using multivariate analysis (relative risk, 2.406; 95% confidence interval, 1.017-5.691; P=0.046). 30881512

2019

dbSNP: rs17026425
rs17026425
0.010 GeneticVariation BEFREE We observed suggestive evidence (<i>P</i> < 0.05) for eight variants (rs17026425, rs17057166, rs6854845, rs1728400, rs17693104, rs202280, rs6797464, and rs823920) in all colorectal cancer and two variants (rs17026425 and rs6854845) in rectal cancer that were concordant with previous reports. 31488414

2019

dbSNP: rs1725459
rs1725459
0.010 GeneticVariation BEFREE In overall and subgroup (defined via body mass index, exercise, and dietary-fat intake) analyses, we identified 2 SNPs (<i>LINC00460</i> rs1725459 and <i>MTRR</i> rs722025) and lifetime cumulative exposure to estrogen (oral contraceptive use) and cigarette smoking as the most common and strongest predictive markers for colorectal cancer risk across the analyses. 31554631

2019

dbSNP: rs17735387
rs17735387
0.010 GeneticVariation BEFREE Gender stratification analysis found that rs7336610, rs7318578, rs17735387, and rs1428 were significantly associated with colorectal cancer risk in males. 30941921

2019

dbSNP: rs2075241
rs2075241
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167

2019

dbSNP: rs2281611
rs2281611
0.010 GeneticVariation BEFREE Genetic associations between the miRNA polymorphisms miR-130b (rs373001), miR-200b (rs7549819), and miR-495 (rs2281611) and colorectal cancer susceptibility. 31117970

2019

dbSNP: rs2284396
rs2284396
0.010 GeneticVariation BEFREE We studied thirteen single nucleotide polymorphisms (SNPs) located in SFRP3 (rs7775), CTNNB1 (β-catenin) [rs4135385, rs13072632], APC (rs454886, rs459552), LRP6 (rs2075241, rs2284396), DKK4 (rs3763511), DKK3 (rs6485350), TCF4 (rs12255372) and AXIN2 (rs3923086, rs3923087, rs4791171) in patients with colorectal cancer (n = 122) and controls (n = 110). 31485167

2019

dbSNP: rs2632159
rs2632159
0.010 GeneticVariation BEFREE lncRNA-<i>PCAT1</i> rs2632159 polymorphism could be a biomarker for colorectal cancer susceptibility. 31253700

2019