4.8 Article

Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

Journal

NATURE GENETICS
Volume 42, Issue 11, Pages 973-U89

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ng.670

Keywords

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Funding

  1. Cancer Research UK
  2. Oxford Comprehensive Biomedical Research Centre
  3. EU
  4. Core infrastructure
  5. Centre for Human Genetics, Oxford [075491/Z/04]
  6. Medical Research Council [G0000657-53203]
  7. CORE and Scottish Executive Chief Scientist's Office [K/OPR/2/2/D333, CZB/4/449]
  8. Cancer Research UK [C31250/A10107]
  9. Cancer Research Wales, Tenovus and Wales Gene Park
  10. Academy of Finland
  11. Finnish Cancer Society
  12. Sigrid Juselius Foundation
  13. MRC [MC_U122861325, MC_U127527198, G0301096] Funding Source: UKRI
  14. Cancer Research UK
  15. The Francis Crick Institute [10124] Funding Source: researchfish
  16. Chief Scientist Office [CZB/4/449] Funding Source: researchfish
  17. Medical Research Council [MC_U122861325, MC_U127527198, G0301096] Funding Source: researchfish
  18. Tenovus Cancer Care [PhD2009/L27] Funding Source: researchfish

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Genome-wide association studies (GWAS) have identified ten loci harboring common variants that influence risk of developing colorectal cancer (CRC). To enhance the power to identify additional CRC risk loci, we conducted a meta-analysis of three GWAS from the UK which included a total of 3,334 affected individuals (cases) and 4,628 controls followed by multiple validation analyses including a total of 18,095 cases and 20,197 controls. We identified associations at four new CRC risk loci: 1q41 (rs6691170, odds ratio (OR) = 1.06, P = 9.55 x 10(-10) and rs6687758, OR = 1.09, P = 2.27 x 10(-9)), 3q26.2 (rs10936599, OR = 0.93, P = 3.39 x 10(-8)), 12q13.13 (rs11169552, OR = 0.92, P = 1.89 x 10(-10) and rs7136702, OR = 1.06, P = 4.02 x 10(-8)) and 20q13.33 (rs4925386, OR = 0.93, P = 1.89 x 10(-10)). In addition to identifying new CRC risk loci, this analysis provides evidence that additional CRC-associated variants of similar effect size remain to be discovered.

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