Interpreting polygenic scores, polygenic adaptation, and human phenotypic differences

80Citations
Citations of this article
221Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Recent analyses of polygenic scores have opened new discussions concerning the genetic basis and evolutionary significance of differences among populations in distributions of phenotypes. Here, we highlight limitations in research on polygenic scores, polygenic adaptation and population differences. We show how genetic contributions to traits, as estimated by polygenic scores, combine with environmental contributions so that differences among populations in trait distributions need not reflect corresponding differences in genetic propensity. Under a null model in which phenotypes are selectively neutral, genetic propensity differences contributing to phenotypic differences among populations are predicted to be small. We illustrate this null hypothesis in relation to health disparities between African Americans and European Americans, discussing alternative hypotheses with selective and environmental effects. Close attention to the limitations of research on polygenic phenomena is important for the interpretation of their relationship to human population differences.

Cite

CITATION STYLE

APA

Rosenberg, N. A., Edge, M. D., Pritchard, J. K., & Feldman, M. W. (2019). Interpreting polygenic scores, polygenic adaptation, and human phenotypic differences. Evolution, Medicine and Public Health, 2019(1), 26–34. https://doi.org/10.1093/emph/eoy036

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free