Genome-wide meta-analysis of quantitatively measured generalized anxiety symptoms in individuals of European ancestry
- Megan Skelton
- Brittany L. Mitchell
- Elham Assary
- Danyang Li
- Genevieve Morneau-Vaillancourt
- Alan E. Murphy
- Abigail R. ter Kuile
- Rujia Wang
- Mark J. Adams
- Enda M. Byrne
- Elizabeth C. Corfield
- Poppy Z. Grimes
- Laurie J. Hannigan
- Jihua Hu
- Kadri Kõiv
- Alex S. F. Kwong
- Sergi Papiol
- Johanne H. Pettersen
- Giorgio Pistis
- Enrique Castelao
- Nora I. Strom
- Peter J. van der Most
- Silviu-Alin Bacanu
- Rosa Cheesman
- Kirstin L. Purves
- Hüseyin Gedik
- Annika B. Faucon
- Kritika Singh
- Lucia Colodro-Conde
- Kristi Krebs
- Per Hoffmann
- Stefan Herms
- Jan Gehlen
- Stephan Ripke
- Swapnil Awasthi
- Teemu Palviainen
- Elisa M. Tasanko
- Roseann E. Peterson
- Daniel E. Adkins
- Andrey A. Shabalin
- Matthew H. Iveson
- Archie Campbell
- Laurent F. Thomas
- Bendik S. Winsvold
- Ole Kristian Drange
- Sigrid Børte
- Tan-Hoang Nguyen
- Sandra M. Meier
- Daniel F. Levey
- Darina Czamara
2026-06-09
Anxiety is heritable and exists on a continuum, with symptoms ranging from adaptive threat response to clinical disorder. Here we performed a genome-wide association meta-analysis of generalized anxiety symptom severity in 693,869 individuals of European ancestry from 14 cohorts. We identified 80 independent genome-wide significant variants within 74 loci, 39 of which were newly associated with anxiety. SNP-based heritability was 5.9% (posterior s.d. = 0.15%). Polygenic scores were significantly associated with anxiety symptom severity and disorder in European, African and South Asian ancestry samples ( R 2 = 1.2–2.9%). Significant genetic correlations ( r g ) were estimated with mental and physical health traits, including case–control anxiety, neuroticism and depression ( r g = 0.71–0.85), irritable bowel syndrome ( r g = 0.57), coronary artery disease, endometriosis and migraine ( r g = 0.20–0.27). Gene-based and pathway analyses implicated synaptic and axonal processes, with enriched expression in the brain. These findings highlight the discovery power gained from analysing a quantitative trait rather than a case–control phenotype in anxiety genetics.