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Volume 613 Issue 7944, 19 January 2023

Lines of descent

The historic isolation of Finland’s population has resulted in a genetic make-up that is relatively homogeneous (as illustrated on the cover). In this week’s issue, two papers make use of Finland’s unique heritage to probe the genetics of disease. At the heart of this work is the FinnGen study, which aims to explore the genomes and health data of 500,000 Finns. The first paper analyses data from 224,737 Finns, finding 1,838 genetic variants that influence 681 different diseases. These include 702 potentially novel, low-frequency variant associations. The second paper focuses on recessive conditions — in which the genes inherited from each parent must both be defective to cause disease — finding a number of Finnish-specific associations and uncovering a larger complexity of genetic inheritance than previously appreciated.

Cover image: Federico Simeoni, Małgorzata Nowicka, Nicola Cerioli, Rupesh Vyas

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