Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13181
rs13181
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE However, no significant difference was found between the ERCC2 rs13181 polymorphism and the risk of pancreatic cancer in the codominant, dominant, and recessive models. 27051038

2016

dbSNP: rs13181
rs13181
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE The increasing evidence of XPD-Lys751Gln impact on the outcome of gemcitabine-cisplatin-based polychemotherapy leads to plan prospective studies to validate the role of this polymorphism as a new tool for optimization of the currently available treatments in pancreatic cancer. 23390054

2013

dbSNP: rs13181
rs13181
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE The XPD Asp312Asn and Lys751Gln polymorphisms, corresponding haplotype, and pancreatic cancer risk. 16458430

2007

dbSNP: rs1799782
rs1799782
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE The present meta-analysis showed significant associations between deoxyribonucleic acid (DNA) repair gene (X-ray repair cross-complementing group 1 (XRCC1) Arg399GIn and Arg194Trp, excision repair cross complementation 1 (ERCC1) rs11615 and rs3212986, ERCC2 rs13181) polymorphisms and PC risk. 31393355

2019

dbSNP: rs1799782
rs1799782
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE This study examined the main and interactive effect of 9 single-nucleotide polymorphisms (SNPs) (Arg194Trp, Arg280His, Arg399Gln, c.1254C>T, c.1517G>C, c.1471G>A, C310T, 539del542, and T1915C) of XRCC1 in contribution to pancreatic cancer (PC). 26418909

2016

dbSNP: rs1799782
rs1799782
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE In conclusion, we found that XRCC1 Arg399Gln genetic variations are associated with pancreatic cancer development, whereas the XRCC1 Arg280His and Arg194Trp polymorphisms did not affect pancreatic cancer risk. 27323136

2016

dbSNP: rs1799782
rs1799782
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE In the subgroup analysis based on ethnicity, there was no statistically significant association between XRCC1 rs1799782 genetic polymorphism and pancreatic cancer risk in Asians/Caucasians under all genetic models (all P values > 0.05). 24435745

2014

dbSNP: rs1799782
rs1799782
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE Yet only one polymorphism, XRCC1 Arg194Trp, appears to be involved in smoking-related cancers and in early onset pancreatic cancer. 17397816

2007

dbSNP: rs1799782
rs1799782
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 GeneticVariation BEFREE We investigated the association between polymorphisms of MGMT (Leu(84)Phe and Ile(143)Val), APE1 (Asp(148)Glu), and XRCC1 (Arg(194)Trp and Arg(399)Gln) and risk of pancreatic cancer in a case-control study. 16844323

2006

dbSNP: rs1217691063
rs1217691063
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE MTHFR gene C677T rather than A1298C polymorphism may be associated with PC. 31701291

2020

dbSNP: rs1217691063
rs1217691063
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE We performed a meta-analysis of all relevant case-control studies that examined the association between MTHFR C677T polymorphism and pancreatic cancer risk. 23098468

2012

dbSNP: rs1217691063
rs1217691063
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE The risk for PC was higher in individuals with MTHFR C677T or TT polymorphisms and a smoking habit (OR = 2.52, 95% CI = 1.05-6.09, P = 0.04). 21441790

2011

dbSNP: rs1217691063
rs1217691063
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE We conducted a case-control study to assess the effect of alcohol on pancreatic cancer in conjunction with polymorphisms in one-carbon metabolism enzymes, methylenetetrahydrofolate reductase (MTHFR C677T), methionine synthase (MTR A2756G), methionine synthase reductase (MTRR A66G), and thymidylate synthase (TS) variable number of tandem repeat. 18843018

2008

dbSNP: rs1217691063
rs1217691063
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE Joint effect between MTHFR C677T polymorphism and smoking or drinking increased risk of pancreatic cancer in a super-multiplicative manner. 16234002

2005

dbSNP: rs397507444
rs397507444
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE MTHFR gene C677T rather than A1298C polymorphism may be associated with PC. 31701291

2020

dbSNP: rs397507444
rs397507444
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE This meta-analysis indicated that MTHFR polymorphisms (C667T and A1298C) were not associated with pancreatic cancer risk. 22901202

2012

dbSNP: rs397507444
rs397507444
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE This meta-analysis indicated that MTHFR polymorphisms (C667T and A1298C) are not associated with pancreatic cancer risk. 23167392

2012

dbSNP: rs397507444
rs397507444
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE We found that the C667T (but not the A1298C) polymorphism had a significant main effect on the risk of pancreatic cancer. 15941958

2005

dbSNP: rs397507444
rs397507444
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE First, we performed a case-control study of germline MTHFR polymorphisms (C677T, A1298C) in 303 patients with pancreatic cancer and 305 matched control subjects. 16234003

2005

dbSNP: rs762846821
rs762846821
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE Importantly, FGTI-2734 inhibited the growth of xenografts derived from four patients with pancreatic cancer with mutant KRAS (2 G12D and 2 G12V) tumors. 31227505

2019

dbSNP: rs762846821
rs762846821
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE K-ras<sup>LSL-G12D/+</sup>:: p53<sup>LSL-R172H/+</sup>:: Pdx-1-Cre (KPC) mice are an established model of pancreatic cancer that specifically express mutants of both K-ras and p53 in the pancreas by using Pdx-1-Cre. 28971839

2018

dbSNP: rs762846821
rs762846821
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE These results suggest that tsTAg synergistically promotes Kras(G12D) -associated PDAC formation, and our study identifies a new mouse model of PDAC that may allow a better understanding of the mechanism of carcinogenesis in pancreatic carcinoma, which shows a catastrophic clinical course. 25042889

2014

dbSNP: rs762846821
rs762846821
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE The concomitant expression of oncogenic Kras(G12D) and mutant p53 (Trp53(R172H)) in the murine pancreas results in metastatic PDA that recapitulates the cognate features of human pancreatic cancer providing an excellent animal model to identify genes required for tumor progression. 22158044

2012

dbSNP: rs762846821
rs762846821
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.050 GeneticVariation BEFREE Using the whole-cell recording mode of the patch-clamp technique, functional ion channels were electrophysiologically characterized in PANC-1 (K-ras G12D (+/-), p53 R273C, Deltap16), BxPC-3 (smad4-, p53 Y220C, Deltap16), and MiaPaCa-2 [transforming growth factor-beta receptor type II defect, K-ras G12C(-/-), p53 R248W, Deltap16] human pancreatic cancer cell lines. 14978241

2004

dbSNP: rs17107315
rs17107315
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.040 GeneticVariation BEFREE Patients with the N34S mutation presented with earlier symptom onset and more dilatation of the main pancreatic duct, followed by more frequent surgical and/or endoscopic intervention and pancreatic cancer development than those without SPINK1 mutations. 17238043

2007