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  • Speedy, Helen E. (author)

A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia

  • Article/chapterEnglish2014

Publisher, publication year, extent ...

  • 2013-12-01
  • Springer Science and Business Media LLC,2014
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-216735
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-216735URI
  • https://doi.org/10.1038/ng.2843DOI
  • https://lup.lub.lu.se/record/4225448URI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:128003913URI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-85627URI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Genome-wide association studies (GWAS) of chronic lymphocytic leukemia (CLL) have shown that common genetic variation contributes to the heritable risk of CLL. To identify additional CLL susceptibility loci, we conducted a GWAS and performed a meta-analysis with a published GWAS totaling 1,739 individuals with CLL (cases) and 5,199 controls with validation in an additional 1,144 cases and 3,151 controls. A combined analysis identified new susceptibility loci mapping to 3q26.2 (rs10936599, P = 1.74 x 10(-9)), 4q26 (rs6858698, P = 3.07 x 10(-9)), 6q25.2 (IPCEF1, rs2236256, P = 1.50 x 10(-10)) and 7q31.33 (POT1, rs17246404, P = 3.40 x 10(-8)). Additionally, we identified a promising association at 5p15.33 (CLPTM1L, rs31490, P = 1.72 x 10(-7)) and validated recently reported putative associations at 5p15.33 (TERT, rs10069690, P = 1.12 x 10(-10)) and 8q22.3 (rs2511714, P = 2.90 x 10(-9)). These findings provide further insights into the genetic and biological basis of inherited genetic susceptibility to CLL.

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Related titles

  • In:Nature Genetics: Springer Science and Business Media LLC46:1, s. 56-+1061-40361546-1718

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