Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

Nat Genet. 2008 Mar;40(3):281-3. doi: 10.1038/ng.89. Epub 2008 Feb 10.

Abstract

We conducted a genome-wide SNP association study on prostate cancer on over 23,000 Icelanders, followed by a replication study including over 15,500 individuals from Europe and the United States. Two newly identified variants were shown to be associated with prostate cancer: rs5945572 on Xp11.22 and rs721048 on 2p15 (odds ratios (OR) = 1.23 and 1.15; P = 3.9 x 10(-13) and 7.7 x 10(-9), respectively). The 2p15 variant shows a significantly stronger association with more aggressive, rather than less aggressive, forms of the disease.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Case-Control Studies
  • Chromosomes, Human, Pair 2*
  • Chromosomes, Human, X*
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Genetic Testing
  • Humans
  • Iceland
  • Linkage Disequilibrium
  • Male
  • Netherlands
  • Polymorphism, Single Nucleotide*
  • Prostatic Neoplasms / genetics*
  • Spain
  • Sweden
  • United States