Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs401681
rs401681
0.740 GeneticVariation BEFREE A small number of common susceptibility loci have been identified for pancreatic cancer, one of which is marked by rs401681 in the TERT-CLPTM1L gene region on chromosome 5p15.33. 25940397

2015

dbSNP: rs401681
rs401681
0.740 GeneticVariation BEFREE This meta-analysis suggests that T allele of CLPTM1L-telomerase reverse transcriptase rs401681 polymorphism is associated with an increased PC risk, especially among Chinese. 25284078

2015

dbSNP: rs505922
rs505922
ABO
0.740 GeneticVariation BEFREE This study provided evidence of SNP rs505922 C allele as a strong risk factor of cancer susceptibility, specifically for pancreatic cancer. 25656610

2015

dbSNP: rs401681
rs401681
0.740 GeneticVariation BEFREE Our data suggests that the T allele of rs401681 in CLPTM1L-TERT locus predisposes its carriers to pancreatic cancer, and further research into the function of CLPTM1L-TERT locus and its potential biological mechanism association may be warranted. 24577890

2014

dbSNP: rs401681
rs401681
0.740 GeneticVariation BEFREE These findings suggested that rs401681 C allele was a low-penetrance risk allele for the development of cancers of lung, bladder, prostate and basal cell carcinoma, but a potential protective allele for melanoma and pancreatic cancer. 23226346

2012

dbSNP: rs505922
rs505922
ABO
0.740 GeneticVariation BEFREE SNP rs505922, located within the first intron of the ABO gene, has been associated with the adenocarcinoma subtype of pancreatic cancer. 22642827

2012

dbSNP: rs505922
rs505922
ABO
0.740 GeneticVariation BEFREE Consistent with earlier reports showing a higher risk of PC for individuals with the non-O blood type, the previously reported protective allele (T) for rs505922 was found to be strongly correlated (r(2) = 0.96) with the O allele. 21306478

2011

dbSNP: rs401681
rs401681
T 0.740 GeneticVariation GWASDB A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. 20101243

2010

dbSNP: rs505922
rs505922
ABO
C 0.740 GeneticVariation GWASDB We identified an association between a locus on 9q34 and pancreatic cancer marked by the SNP rs505922 (combined P = 5.37 x 10(-8); multiplicative per-allele odds ratio 1.20; 95% confidence interval 1.12-1.28). 19648918

2009

dbSNP: rs505922
rs505922
ABO
0.740 GeneticVariation BEFREE We identified an association between a locus on 9q34 and pancreatic cancer marked by the SNP rs505922 (combined P = 5.37 x 10(-8); multiplicative per-allele odds ratio 1.20; 95% confidence interval 1.12-1.28). 19648918

2009

dbSNP: rs3790844
rs3790844
0.730 GeneticVariation BEFREE Our results showed that the rs3790843 (GA vs GG: OR=0.86, CI=0.76-0.98, <i>P</i>=0.992; GA+AA vs GG: OR=0.83, CI=0.73-0.94, <i>P</i>=0.950; A vs G: OR=0.85, CI=0.78-0.93, <i>P</i>=0.802), rs3790844 (CC vs TT: OR=0.65, CI=0.54-0.78, <i>P</i>=0.617; CC vs TT+CT: OR=0.73, CI=0.62-0.85, <i>P</i>=0.742; C vs T: OR=0.78, CI=0.73-0.84, <i>P</i>=0.555) and rs12029406 (TT vs CC: OR=0.73, CI=0.61-0.89, <i>P</i>=0.483; TT vs CC+CT: OR=0.78, CI=0.66-0.92, <i>P</i>=0.648; T vs C: OR=0.87, CI=0.79-0.95, <i>P</i>=0.837) polymorphisms were associated statistically with the risk of pancreatic cancer. 29785120

2018

dbSNP: rs3790844
rs3790844
0.730 GeneticVariation BEFREE In previously reported pancreatic cancer-associated SNPs, rs3790844 (NR5A2) showed a significant correlation with PDAC in our cohort. 28639428

2018

dbSNP: rs3790844
rs3790844
0.730 GeneticVariation BEFREE Our case-control study found that rs3790843 and rs3790844 in the NR5A2 gene are associated with pancreatic cancer risk in Japanese subjects. 26592175

2015

dbSNP: rs3790844
rs3790844
T 0.730 GeneticVariation GWASDB A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. 20101243

2010

dbSNP: rs10500715
rs10500715
T 0.700 GeneticVariation GWASDB Genome-wide association study of survival in patients with pancreatic adenocarcinoma. 23180869

2014

dbSNP: rs12362504
rs12362504
0.700 GeneticVariation GWASDB Genome-wide association study of survival in patients with pancreatic adenocarcinoma. 23180869

2014

dbSNP: rs12456874
rs12456874
G 0.700 GeneticVariation GWASDB Genome-wide association study of survival in patients with pancreatic adenocarcinoma. 23180869

2014

dbSNP: rs7106914
rs7106914
0.700 GeneticVariation GWASDB Genome-wide association study of survival in patients with pancreatic adenocarcinoma. 23180869

2014

dbSNP: rs1153280
rs1153280
0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. 22158540

2011

dbSNP: rs1153287
rs1153287
0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. 22158540

2011

dbSNP: rs1153294
rs1153294
0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. 22158540

2011

dbSNP: rs117214
rs117214
0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. 22158540

2011

dbSNP: rs12413624
rs12413624
T 0.700 GeneticVariation GWASDB Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. 22158540

2011

dbSNP: rs1447826
rs1447826
0.700 GeneticVariation GWASDB Including additional controls from public databases improves the power of a genome-wide association study. 21849791

2011

dbSNP: rs1455311
rs1455311
0.700 GeneticVariation GWASDB Including additional controls from public databases improves the power of a genome-wide association study. 21849791

2011