rs965513
|
|
|
0.860 |
GeneticVariation |
BEFREE |
The A allele of rs965513 polymorphism was shown to be highly associated with risk of thyr</span>oid cancer, with odds ratios of 1.58 (95% CI 1.32-1.90) in all populations, 1.65 (95% CI 1.31-2.07)) in Caucasian populations and 1.49 in Asian populations.
|
27191655 |
2016 |
rs965513
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations.
|
25855579 |
2015 |
rs965513
|
|
|
0.860 |
GeneticVariation |
BEFREE |
These results explain the mechanism by which the risk allele of rs965513 predisposes to thyroid cancer.
|
25918370 |
2015 |
rs965513
|
|
|
0.860 |
GeneticVariation |
BEFREE |
For rs965513, individuals carrying the risk A allele, compared to individuals with the G allele, had 31 % higher risk of thyroid cancer (A vs. G: OR 1.31, 95 % CI 1.17-1.46).
|
26206751 |
2015 |
rs965513
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
Genome-wide association study on differentiated thyroid cancer.
|
23894154 |
2013 |
rs965513
|
|
A |
0.860 |
GeneticVariation |
GWASDB |
Genome-wide association study on differentiated thyroid cancer.
|
23894154 |
2013 |
rs965513
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Five single nucleotide polymorphisms (SNPs) were previously reported to be associated with thyroid cancer in European populations in two genome-wide association studies (GWAS): rs965513 (9q22.33), rs944289 (14q13.3), rs116909374 (14q13.3), rs966423 (2q35) and rs2439302 (8p12).
|
23847140 |
2013 |
rs965513
|
|
|
0.860 |
GeneticVariation |
BEFREE |
The four validated TC SNPs accounted for a relatively large proportion (∼11%) of the sibling relative risk of TC, principally owing to the large effect size of rs965513 (OR 1.74).
|
22282540 |
2012 |
rs965513
|
|
|
0.860 |
GeneticVariation |
BEFREE |
Of those, rs965513 has previously been shown to associate with thyroid cancer.
|
22267200 |
2012 |
rs965513
|
|
|
0.860 |
GeneticVariation |
GWASDB |
Of those, rs965513 has previously been shown to associate with thyroid cancer.
|
22267200 |
2012 |
rs965513
|
|
|
0.860 |
GeneticVariation |
GWASDB |
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.
|
20350937 |
2010 |
rs965513
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.
|
20350937 |
2010 |
rs965513
|
|
A |
0.860 |
GeneticVariation |
GWASCAT |
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
|
19198613 |
2009 |
rs965513
|
|
A |
0.860 |
GeneticVariation |
GWASDB |
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
|
19198613 |
2009 |