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Clinical relevance of genome-wide polygenic score may be less than claimed.

David Curtis
Published in: Annals of human genetics (2019)
The AUC of the GPS for these diseases is modest. Furthermore, the literature robustly demonstrates that the true CAD risk associated with monogenic mutations is much higher than the threefold increase that is predicted by the GPS. Together, these findings cast doubt on the clinical utility of the GPS.
Keyphrases
  • genome wide
  • systematic review
  • coronary artery disease
  • dna methylation