Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1427471466
rs1427471466
0.010 GeneticVariation BEFREE Variants that disrupted RPS20 were detected in a Finnish family with early-onset CRC (p.Val50SerfsTer23), a 39-year old individual with metachronous CRC (p.Leu61GlufsTer11 mutation), and a 41-year-old individual with CRC (missense p.Val54Leu), but not in controls. 27713038

2017

dbSNP: rs1800371
rs1800371
0.020 GeneticVariation BEFREE TP53 Pro47Ser and Arg72Pro polymorphisms and colorectal cancer predisposition in an ethnic Kashmiri population. 20449797

2010

dbSNP: rs1800371
rs1800371
0.020 GeneticVariation BEFREE On the contrast, all genetic models showed no statistical association of TP53 Pro47Ser polymorphism among CRC patients compared with healthy controls. 29560751

2019

dbSNP: rs28934575
rs28934575
0.010 GeneticVariation BEFREE The other three mutations (Arg175Gly, DeltaPro190, and Gly245Ser) have been found in colorectal carcinomas, the last commonly. 12010886

2002

dbSNP: rs28934576
rs28934576
0.740 GeneticVariation BEFREE We therefore investigated the anti-tumor properties of a gold(I) <i>N</i>-heterocyclic carbene (NHC) complex-termed MC3-in human colorectal cancer (CRC) cell lines encompassing three different p53 variations: HCT116 wild-type (WT), HCT116 p53<sup>-/-</sup>, and HT-29 (mutant; R273H). 31231607

2019

dbSNP: rs28934576
rs28934576
0.740 GeneticVariation BEFREE Finally, lnc273-31 and lnc273-34 were significantly highly expressed in CRC tissues with p53-R273H mutation compared to those with wildtype p53. 31455383

2019

dbSNP: rs28934576
rs28934576
T 0.740 CausalMutation CLINVAR

dbSNP: rs28934576
rs28934576
0.740 GeneticVariation BEFREE Our findings indicate the R270H/R273H p53 mutant protein does not manifest definite GOF biological effects in mouse and human CRCs, suggesting possible GOF effects of mutant p53 in cancer phenotypes are likely allele-specific and/or context-dependent. 31148594

2019

dbSNP: rs28934576
rs28934576
0.740 GeneticVariation BEFREE The CRC colorectal cancer (CRC) cell lines HCT116 wild-type (wt), HCT116 p53-/-, and HT-29 (mutant; R273H) were employed, covering three different p53 variations. 28618116

2017

dbSNP: rs28934578
rs28934578
T 0.700 CausalMutation CLINVAR

dbSNP: rs55832599
rs55832599
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587780071
rs587780071
0.010 GeneticVariation BEFREE Our study is the first study that investigates the relationship among variants of CDKN2 p16 540 C>G, 580 C>T, and MDM2 SNP309 T>G risk of CRC and the development and progression in the Turkish population. 23777425

2013

dbSNP: rs746504075
rs746504075
0.010 GeneticVariation BEFREE Variants that disrupted RPS20 were detected in a Finnish family with early-onset CRC (p.Val50SerfsTer23), a 39-year old individual with metachronous CRC (p.Leu61GlufsTer11 mutation), and a 41-year-old individual with CRC (missense p.Val54Leu), but not in controls. 27713038

2017

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE We searched multiple electronic databases to identify studies investigating the association between the Arg72Pro polymorphism and colorectal cancer. 20615891

2010

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Our data suggest that R72P variant seems to be associated with high risk for development of CRC but carries low risk for development of UC. 20309662

2010

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Association of Arg72Pro of P53 polymorphism with colorectal cancer susceptibility risk in Malaysian population. 22393962

2011

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE We conclude that Arg72Pro SNP is associated with susceptibility to developing CRC in this ethnic Kashmiri population. 20449797

2010

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE The gene-gene interaction between TP53 Arg72Pro and MDM2 T309G may interact in carcinogenesis of CRC in Chinese, especially in smokers, and this kind of interaction is associated with onset age of CRC. 22744426

2012

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE The SNP rs4938723 and diabetes mellitus (DM) together were associated with an increased CRC risk, but the SNP TP53 Arg72Pro CC with DM showed a protective effect against CRC. 24337371

2014

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Unexpectedly no significant association was found between this potential marker TP53 Arg72Pro and CRC (p > 0.05). 25537146

2015

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE We found that the TP53 Arg72Pro polymorphism was not significantly associated with CRC risk in the overall population. 27901479

2017

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE We assessed the association of TP53 Arg72Pro and p53PIN3 polymorphisms with colorectal cancer risk and their possible interaction with nonsteroidal anti-inflammatory drug use. 17622940

2007

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Thus, our current meta-analysis indicates no evidence for the association between the p53 Arg72Pro polymorphism and CRC risk in the Asian population, but significant association in Chinese population, especially for rectal cancer and in men. 30316510

2018

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE The p53 R72P genotype was identified by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method in 78 consecutive colorectal cancer patients with liver metastases and 214 age- and sex-matched cases with nonmetastatic colorectal cancer. 18988302

2008

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Age of diagnosis of CRC in HNPCC patients is therefore more complex than that predicted by the R72P TP53 polymorphism alone, suggesting an inter-relationship with other genetic and/or environmental factors. 16353134

2006