rs8180817
▶GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
insomnia
Watanabe K et al. “Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways.” Nature Genetics 54(8):1125-1132 (2022)
Allele C
OR 0.01
p 1.0e-23
N 2,365,010
Meta-analysisLarge GWAS
European
Song W et al. “Genome-wide association analysis of insomnia using data from Partners Biobank.” Scientific Reports 10(1):6928 (2020)
Allele C
OR —
p 2.0e-8
N 422,239
Large GWAS
multi-ancestry
insomnia measurement
Jansen PR et al. “Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.” Nature Genetics 51(3):394-403 (2019)
Allele G
OR 1.05
p 2.0e-16
N 1,331,010
Large GWAS
European
osteoarthritis
Verma A et al. “Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.” Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.03
p 1.0e-11
N 567,064
Major Consortium StudyLarge GWAS
multi-ancestry
major depressive disorder
Als TD et al. “Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.” Nature Medicine 29(7):1832-1844 (2023)
Allele G
OR 0.02
p 2.0e-11
N 1,349,887
Large GWAS
European
anxiety disorder
Friligkou E et al. “Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study.” Nature Genetics 56(10):2036-2045 (2024)
Allele G
OR —
β 0.012
p 4.0e-9
N 1,096,458
Large GWAS
European
body height
Schoeler T et al. “Participation bias in the UK Biobank distorts genetic associations and downstream analyses.” Nature Human Behaviour 7(7):1216-1227 (2023)
Allele C
OR 0.10
p 3.0e-8
N 283,749
Major Consortium StudyLarge GWAS
European
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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