rs13109404
▶GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
diastolic blood pressure
Plotnikov D et al. “High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study.” Investigative Ophthalmology & Visual Science 63(6):29 (2022)
Allele T
OR 0.54
p 5.0e-34
N 526,001
Large GWAS
European
sleep duration trait
Scammell BH et al. “Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration.” Human Molecular Genetics 32(18):2797-2807 (2023)
Allele T
OR 0.03
p 5.0e-12
N 483,235
Large GWAS
multi-ancestry
Dashti HS et al. “Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.” Nature Communications 10(1):1100 (2019)
Allele T
OR 1.72
p 9.0e-11
N 446,118
Large GWAS
European
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 T
OR 0.03
p 1.0e-11
N 384,317
Large GWAS
European
pappalysin‐1 measurement
Folkersen L et al. “Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.” Nature Metabolism 2(10):1135-1148 (2020)
Allele T
OR 0.14
p 4.0e-11
N 21,758
Large GWAS
European
systolic blood pressure
Teixeira SK et al. “Assessing the predictive efficacy of European-based systolic blood pressure polygenic risk scores in diverse Brazilian cohorts.” Scientific Reports 14(1):28123 (2024)
Allele G
OR 0.71
p 9.0e-11
N 286,581
Large GWAS
European
substance-related disorder
Lai D et al. “Genome-wide meta-analyses of cross substance use disorders in diverse populations.” Molecular Psychiatry 31(3):1619-1633 (2026)
Allele T
OR 8.45
p 3.0e-17
N 1,699,295
Large GWAS
multi-ancestry
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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