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 |
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 |
rs10500715
|
|
T |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of survival in patients with pancreatic adenocarcinoma.
|
23180869 |
2014 |
rs12413624
|
|
T |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs2255280
|
|
T |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs372883
|
|
T |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs80358683
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Nonsense-mediated mRNA decay: terminating erroneous gene expression.
|
15145354 |
2004 |
rs12456874
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of survival in patients with pancreatic adenocarcinoma.
|
23180869 |
2014 |
rs5768709
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs9502893
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of pancreatic cancer in Japanese population.
|
20686608 |
2010 |
rs9573163
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs505922
|
|
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 |
rs397507851
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Nonsense-mediated mRNA decay: terminating erroneous gene expression.
|
15145354 |
2004 |
rs4269383
|
|
C |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs587776416
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs9543325
|
|
C |
0.700 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.
|
20101243 |
2010 |
rs1555461176
|
|
AT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1547374
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs4927850
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
rs6464375
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of pancreatic cancer in Japanese population.
|
20686608 |
2010 |
rs708224
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of pancreatic cancer in Japanese population.
|
20686608 |
2010 |
rs80359584
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Nonsense-mediated mRNA decay: terminating erroneous gene expression.
|
15145354 |
2004 |
rs9363918
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
|
22158540 |
2011 |
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 |
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 |