Inherited genetic susceptibility to multiple myeloma

Research output: Contribution to journalReview article


Although the familial clustering of multiple myeloma (MM) supports the role of inherited susceptibility, only recently has direct evidence for genetic predisposition been demonstrated. A meta-analysis of two genome-wide association (GWA) studies has identified single-nucleotide polymorphisms (SNPs) localising to a number of genomic regions that are robustly associated with MM risk. In this review, we provide an overview of the evidence supporting a genetic contribution to the predisposition to MM and MGUS (monoclonal gammopathy of unknown significance), and the insight this gives into the biological basis of disease aetiology. We also highlight the promise of future approaches to identify further specific risk factors and their potential clinical utility.


  • G. J. Morgan
  • D. C. Johnson
  • N. Weinhold
  • H. Goldschmidt
  • O. Landgren
  • H. T. Lynch
  • Kari Hemminki
  • R. S. Houlston
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Cancer and Oncology


  • myeloma, SNP, MGUS
Original languageEnglish
Pages (from-to)518-524
Issue number3
Publication statusPublished - 2014
Publication categoryResearch