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Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

Crowther-Swanepoel, Dalemari; Broderick, Peter; Di Bernardo, Maria Chiara; Dobbins, Sara E.; Torres, María; Mansouri, Mahmoud; Ruiz-Ponte, Clara; Enjuanes, Anna; Rosenquist, Richard; Carracedo, Angel; Jurlander, Jesper; Campo, Elias; Juliusson, Gunnar; Montserrat, Emilio; Smedby, Karin E.; Dyer, Martin J.S.; Matutes, Estella; Dearden, Claire; Sunter, Nicola J.; Hall, Andrew G.; Mainou-Fowler, Tryfonia; Jackson, Graham H.; Summerfield, Geoffrey; Harris, Robert J.; Pettitt, Andrew R.; Allsup, David J.; Bailey, James R.; Pratt, Guy; Pepper, Chris; Fegan, Chris; Parker, Anton; Oscier, David; Allan, James M.; Catovsky, Daniel; Houlston, Richard S.

Authors

Dalemari Crowther-Swanepoel

Peter Broderick

Maria Chiara Di Bernardo

Sara E. Dobbins

María Torres

Mahmoud Mansouri

Clara Ruiz-Ponte

Anna Enjuanes

Richard Rosenquist

Angel Carracedo

Jesper Jurlander

Elias Campo

Gunnar Juliusson

Emilio Montserrat

Karin E. Smedby

Martin J.S. Dyer

Estella Matutes

Claire Dearden

Nicola J. Sunter

Andrew G. Hall

Tryfonia Mainou-Fowler

Graham H. Jackson

Geoffrey Summerfield

Robert J. Harris

Andrew R. Pettitt

James R. Bailey

Guy Pratt

Chris Pepper

Chris Fegan

Anton Parker

David Oscier

James M. Allan

Daniel Catovsky

Richard S. Houlston



Abstract

To identify new risk variants for chronic lymphocytic leukemia (CLL), we conducted a genome-wide association study of 299,983 tagging SNPs, with validation in four additional series totaling 2,503 cases and 5,789 controls. We identified four new risk loci for CLL at 2q37.3 (rs757978, FARP2; odds ratio (OR) = 1.39; P = 2.11 × 10 9), 8q24.21 (rs2456449; OR = 1.26; P = 7.84 × 10 10), 15q21.3 (rs7169431; OR = 1.36; P = 4.74 × 10 7) and 16q24.1 (rs305061; OR = 1.22; P = 3.60 × 10 7). We also found evidence for risk loci at 15q25.2 (rs783540, CPEB1; OR = 1.18; P = 3.67 × 10 6) and 18q21.1 (rs1036935; OR = 1.22; P = 2.28 × 10 6). These data provide further evidence for genetic susceptibility to this B-cell hematological malignancy. © 2010 Nature America, Inc. All rights reserved.

Citation

Crowther-Swanepoel, D., Broderick, P., Di Bernardo, M. C., Dobbins, S. E., Torres, M., Mansouri, M., Ruiz-Ponte, C., Enjuanes, A., Rosenquist, R., Carracedo, A., Jurlander, J., Campo, E., Juliusson, G., Montserrat, E., Smedby, K. E., Dyer, M. J., Matutes, E., Dearden, C., Sunter, N. J., Hall, A. G., …Houlston, R. S. (2010). Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk. Nature genetics, 42(2), 132-136. https://doi.org/10.1038/ng.510

Journal Article Type Article
Acceptance Date Nov 20, 2009
Online Publication Date Jan 10, 2010
Publication Date Feb 1, 2010
Deposit Date Apr 4, 2022
Publicly Available Date Oct 9, 2024
Journal Nature Genetics
Print ISSN 1061-4036
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 42
Issue 2
Pages 132-136
DOI https://doi.org/10.1038/ng.510
Public URL https://hull-repository.worktribe.com/output/3578035

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Copyright Statement
This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: https://doi.org/10.1038/ng.510






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