Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16906252
rs16906252
0.010 GeneticVariation BEFREE Other SNPs associated with the risk of colon cancer (e.g., rs16906252 in MGMT) were found to affect mRNA expression levels in colon transverse and therefore working as possible cis-eQTL suggesting possible mechanisms of carcinogenesis. 31209889

2020

dbSNP: rs11646171
rs11646171
0.010 GeneticVariation BEFREE We found looping chromatin interactions between non-coding regions at 6p25.3 (rs11646171) with the IRF4 promoter and at 8q24.21 (rs13254990) with the MYC promoter, both genes with strong relevance to B-cell tumorigenesis. 31102405

2019

dbSNP: rs119484086
rs119484086
0.010 GeneticVariation BEFREE One rare missense variant associated with the occurrence of prostate cancer (p.Arg781His) impairs the mitochondrial RNase Z activity of ELAC2, suggesting a functional link between tumorigenesis and mitochondrial RNA metabolism. 31045291

2019

dbSNP: rs121912660
rs121912660
0.010 GeneticVariation BEFREE The K120R mutation renders the p53 protein disabled for acetylation and, as a result, defective for apoptotic function, which provides a mechanistic link between the missense mutation and tumorigenesis. 30348990

2019

dbSNP: rs13254990
rs13254990
0.010 GeneticVariation BEFREE We found looping chromatin interactions between non-coding regions at 6p25.3 (rs11646171) with the IRF4 promoter and at 8q24.21 (rs13254990) with the MYC promoter, both genes with strong relevance to B-cell tumorigenesis. 31102405

2019

dbSNP: rs13428812
rs13428812
0.010 GeneticVariation BEFREE However, rs13428812 was not associated with severe gastric mucosal atrophy or gastric carcinogenesis. 30867787

2019

dbSNP: rs1400826115
rs1400826115
0.010 GeneticVariation BEFREE Our results suggest that XPD G751A, hOGG1 C326G and XRCC4 G1394T gene polymorphisms might play an important role in colorectal carcinogenesis and increase the risk of developing CRC in the Chinese Han population. 30429230

2019

dbSNP: rs1453340173
rs1453340173
0.010 GeneticVariation BEFREE We substituted Val285 with Ala (V285A) in an Ala-Val dipeptide, to mimic the conserved Ala-Ala in many members of the basic leucine-zipper family of transcription factors, important in gene regulation, cell proliferation and oncogenesis. 30566668

2019

dbSNP: rs17878467
rs17878467
0.010 GeneticVariation BEFREE What's more, rs17878467 polymorphism may play a protect role in the tumorigenesis of urinary cancer, shown in heterozygote comparison model (MW vs. WW: OR = 0.882, 95% CI = 0.78-0.999, P = 0.048). 30463805

2019

dbSNP: rs1799983
rs1799983
0.010 GeneticVariation BEFREE In conclusion, although eNOS SNPs rs2070744 and rs1799983 do not display significant associations with cervical carcinogenesis and patient survival, cervical cancer patients with genotypes TC/CC in rs2070744 carry less risk of advanced stage, parametrium invasion and pelvic lymph node metastasis in Taiwan. 31258766

2019

dbSNP: rs2001389
rs2001389
0.010 GeneticVariation BEFREE By integrating analysis on multiomics data, association studies and functional assays, we proposed that the common variant rs2001389 and the gene MFSD13A might be genetic modifiers of PC tumorigenesis. 31237042

2019

dbSNP: rs2070744
rs2070744
0.010 GeneticVariation BEFREE In conclusion, although eNOS SNPs rs2070744 and rs1799983 do not display significant associations with cervical carcinogenesis and patient survival, cervical cancer patients with genotypes TC/CC in rs2070744 carry less risk of advanced stage, parametrium invasion and pelvic lymph node metastasis in Taiwan. 31258766

2019

dbSNP: rs2073859
rs2073859
0.010 GeneticVariation BEFREE As the mechanisms of LIMK-associated tumorigenesis are still unclear, we analyzed the tumorigenic functions of LIM kinase 2 (LIMK2) in human bladder cancer (BC) and explored whether the newly identified LIMK2 3´-UTR SNP rs2073859 (G-to-A allele) is correlated with clinical features. 30006972

2019

dbSNP: rs2276466
rs2276466
0.010 GeneticVariation BEFREE The rs2276466 polymorphism might play different roles in carcinogenesis of various cancer types. 31040199

2019

dbSNP: rs2423279
rs2423279
0.010 GeneticVariation BEFREE Our results suggest that SNP rs4444235 at 14q22.2 and SNP rs2423279 at 20p12.3 may interact with regular exercise and aspirin use in colorectal carcinogenesis. 31849324

2019

dbSNP: rs2682818
rs2682818
0.010 GeneticVariation BEFREE Piles of evidence have supported the relationship between miR-618 rs2682818 polymorphism and tumorigenesis, but the conclusion remains inconsistent. 31383788

2019

dbSNP: rs3819102
rs3819102
0.010 GeneticVariation BEFREE The C allele of rs3819102 is the risk allele for lung carcinogenesis in a dominant model (OR, 1.435; 95% CI, 1.188-1.735). 30180988

2019

dbSNP: rs4444235
rs4444235
0.010 GeneticVariation BEFREE Our results suggest that SNP rs4444235 at 14q22.2 and SNP rs2423279 at 20p12.3 may interact with regular exercise and aspirin use in colorectal carcinogenesis. 31849324

2019

dbSNP: rs5743836
rs5743836
0.010 GeneticVariation BEFREE Our findings show that TLR9 rs5743836 and rs187084 polymorphisms are associated with a higher risk of carcinogenesis gastric, and that TLR9 mRNA levels can be modulated by TLR9-1237 TC + CC variant genotypes and <i>H. pylori</i> infection. 31798780

2019

dbSNP: rs664589
rs664589
0.010 GeneticVariation BEFREE <i>In vitro</i> and <i>in vivo</i> experiments showed that the rs664589 C to G mutation facilitated carcinogenesis and metastasis of colorectal cancer. 31311811

2019

dbSNP: rs764803020
rs764803020
0.010 GeneticVariation BEFREE The K120R mutation renders the p53 protein disabled for acetylation and, as a result, defective for apoptotic function, which provides a mechanistic link between the missense mutation and tumorigenesis. 30348990

2019

dbSNP: rs7717457
rs7717457
0.010 GeneticVariation BEFREE <b>Conclusions</b>: SNP rs7717457 is associated with the selection of HBV BCP double mutations, providing an important clue to understanding the mechanisms of oncogenesis of HBV BCP double mutations. 31341412

2019

dbSNP: rs7726159
rs7726159
0.010 GeneticVariation BEFREE In conclusion, the functional variant rs7726159 confers lung cancer susceptibility might by affecting MYC binding and inducing telomere lengthening, which provides a new insight into the crucial role of telomere biology in tumorigenesis. 30680798

2019

dbSNP: rs781490101
rs781490101
0.010 GeneticVariation BEFREE The K120R mutation renders the p53 protein disabled for acetylation and, as a result, defective for apoptotic function, which provides a mechanistic link between the missense mutation and tumorigenesis. 30348990

2019

dbSNP: rs1057519853
rs1057519853
0.010 GeneticVariation BEFREE Whereas Q209L accounts for approximately half of GNAQ mutations in UM, Q209P is as frequent as Q209L and also promotes oncogenesis, but has not been characterized at the molecular level. 30352874

2018