rs4409766

GWAS Catalog Trait Associations (8)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

body mass index

Allele C
OR 0.03
p 6.0e-17
N 158,284
Large GWAS
multi-ancestry
Allele C
OR
β 0.029
p 2.0e-12
N 334,487
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.02
p 6.0e-12
N 163,835
Large GWAS
East Asian

systolic blood pressure

Allele T
OR 1.24
p 6.0e-17
N 11,816
Large GWAS
East Asian
Allele T
OR 0.58
p 3.0e-12
N 130,777
Large GWAS
multi-ancestry

diastolic blood pressure

Allele T
OR 0.59
p 6.0e-13
N 11,816
Large GWAS
East Asian
Li C et al. Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians. Circulation. Cardiovascular Genetics 10(2):e001527 (2017)
Allele T
OR 0.40
p 8.0e-9
N 18,422
Meta-analysisLarge GWAS
multi-ancestry

hypertension

Allele T
OR
p 7.0e-13
N 9,469
Large GWAS
East Asian
Allele T
OR 0.09
p 4.0e-10
N 50,792
Large GWAS
multi-ancestry

mean arterial pressure

Li C et al. Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians. Circulation. Cardiovascular Genetics 10(2):e001527 (2017)
Allele T
OR 0.54
p 1.0e-11
N 18,422
Meta-analysisLarge GWAS
multi-ancestry
Allele T
OR 0.33
p 3.0e-8
N 130,777
Large GWAS
multi-ancestry

pulse pressure measurement

Allele T
OR 0.38
p 2.0e-11
N 130,777
Large GWAS
multi-ancestry

angina pectoris

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.11
p 3.0e-10
N 608,573
Large GWAS
multi-ancestry

wellbeing measurement

Baselmans BML et al. Multivariate genome-wide analyses of the well-being spectrum. Nature Genetics 51(3):445-451 (2019)
Allele C
OR 0.01
p 2.0e-8
N 2,083,151
Large GWAS
European

Research that mentions this SNP (1)

A Comprehensive Family-Based Replication Study of Schizophrenia Genes
AssociationN=28,251Karolina A. Aberg et al.(2013)· JAMA Psychiatry

This comprehensive family-based replication study tested 8,107 SNPs in 6,298 individuals (3,286 schizophrenia cases) from 1,811 nuclear families, following a meta-analysis of 18 schizophrenia GWAS studies. The study replicated major findings in TCF4 (P=2.53×10⁻¹⁰) and NOTCH4 (P=3.16×10⁻⁷), and identified novel susceptibility loci including POM121L2 (P=3.51×10⁻⁷), AS3MT (P=9.01×10⁻⁷), CNNM2 (P=6.07×10⁻⁷), and NT5C2 (P=4.09×10⁻⁷). Pathway analyses revealed significant enrichment in neuronal function (axonal guidance, neuronal systems, L1 cell adhesion) and immune system pathways (antigen processing, T-cell adhesion molecules).

Traits studied:Schizophrenia

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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