Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3731249
rs3731249
0.030 GeneticVariation BEFREE The obtained results allow us to conclude: (i) survival times of 500 C/G carriers vs. cumulating proportion surviving was not statistically significant; (ii) CDKN2a polymorphism 500 C/G correlated with Ala148Thr; (iii) no correlation was observed between the 500 C/G polymorphism and age of diagnosis, localization of primary melanoma and survival time; (iv) we did not find correlation between 500 C/G and type of cancer in the family; (v) changes in the CDKN2a gene were not found in patients with second cancer. 17351674

2007

dbSNP: rs3731249
rs3731249
0.030 GeneticVariation BEFREE These results suggest that A148T variant may be associated with a multi-organ cancer risk in the Polish population. 16395703

2006

dbSNP: rs3731249
rs3731249
0.030 GeneticVariation BEFREE The A148T carrier population (heterozygous G/A alleles) was more likely to have a relative with malignancy compared with the noncarrier population (57% versus 36%, respectively; P = 0.03). 15705881

2005

dbSNP: rs11515
rs11515
0.010 GeneticVariation BEFREE In addition, CDKN2A rs11515 polymorphism might associate with cancer risk in Asians. 28466822

2017

dbSNP: rs200863613
rs200863613
0.010 GeneticVariation BEFREE Dysfunction of individual annexin and S100A proteins is associated with cancer progression, metastasis and cancer drug resistance. 28068434

2017

dbSNP: rs3088440
rs3088440
0.010 GeneticVariation BEFREE Overall, we found that rs3731249, rs11515, and rs3088440 polymorphisms were not associated with cancer risk (OR=1.27, 95%CI: 0.79-2.03; OR=0.91, 95%CI: 0.79-1.03; OR=1.02, 95%CI: 0.95-1.09). 28466822

2017

dbSNP: rs1444669684
rs1444669684
0.010 GeneticVariation BEFREE In conclusion, our results illustrate that the K-Ras(V14I) activating protein is able to induce cancer, although at a much lower level than the classical K-Ras(G12V) oncogene, and that it can be significantly modulated by both genetic and non-genetic events. 27174785

2016

dbSNP: rs771138120
rs771138120
0.010 GeneticVariation BEFREE The importance of the CDK4 locus in human cancer first became evident following the identification of a germ line CDK4-Arg24Cys (R24C) mutation, which abolishes the ability of CDK4 to bind to p16(INK4a). 11756559

2002