Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk

  • N Orr
  • , A Lemnrau
  • , R Cooke
  • , O Fletcher
  • , K Tomczyk
  • , M Jones
  • , N Johnson
  • , CJ Lord
  • , C Mitsopoulos
  • , M Zvelebil
  • , SS McDade
  • , G Buck
  • , C Blancher
  • , AH Trainer
  • , PA James
  • , SE Bojesen
  • , S Bokmand
  • , H Nevanlinna
  • , J Mattson
  • , E Friedman
  • Y Laitman, D Palli, G Masala, I Zanna, L Ottini, G Giannini, Antoinette Hollestelle, Ans van den Ouweland, S Novakovic, M Krajc, M Gago-Dominguez, JE Castelao, H Olsson, I Hedenfalk, DF Easton, PDP Pharoah, AM Dunning, DT Bishop, SL Neuhausen, L Steele, RS Houlston, M Garcia-Closas, A Ashworth, AJ Swerdlow

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94 Citations (Scopus)

Abstract

We conducted a genome-wide association study of male breast cancer comprising 823 cases and 2,795 controls of European ancestry, with validation in independent sample sets totaling 438 cases and 474 controls. A SNP in RAD51B at 14q24.1 was significantly associated with male breast cancer risk (P = 3.02 x 10(-13); odds ratio (OR) = 1.57). We also refine association at 16q12.1 to a SNP within TOX3 (P = 3.87 x 10(-15); OR = 1.50).
Original languageUndefined/Unknown
Pages (from-to)1182-1184
Number of pages3
JournalNature Genetics
Volume44
Issue number11
DOIs
Publication statusPublished - 2012

Research programs

  • EMC MGC-02-96-01

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