rs17465637

This variant is located in the MIA3 gene.

GWAS Catalog Trait Associations (2)

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

coronary artery disease

Allele C
OR 0.08
p 8.0e-31
N 250,736
Large GWAS
Allele C
OR 1.14
p 1.0e-8
N 86,995
Large GWAS
European

myocardial infarction

Allele C
OR 0.11
p 2.0e-12
N 394,626
Large GWAS
European
Allele C
OR 1.14
p 1.0e-9
N 6,042
Large GWAS
European

ClinVar annotation

Benign☆☆☆
1 submitter1 publication

Coronary artery disorder

View on ClinVar →

Research that mentions this SNP (3)

Common genetic polymorphisms in Moyamoya and atherosclerotic disease in Europeans
AssociationN=108Constantin Roder et al.(2011)· Child's Nervous System

Case-control study of 40 European Moyamoya disease patients versus 68 controls found a significant association between rs599839 (A/G, OR=2.17, 95% CI=1.17-4.05, p=0.01) in the PSRC1 gene and Moyamoya disease, along with three additional SNPs showing borderline significance in ELN and CXCL12 genes. The findings suggest shared genetic pathways between Moyamoya disease and atherosclerotic disease.

Traits studied:Atherosclerotic diseaseMoyamoya disease
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts
AssociationN=33,282Juha Karvanen et al.(2009)· Genetic Epidemiology

Prospective cohort study of 33,282 individuals from the MORGAM Project investigating SNPs from recent GWAS in relation to incident coronary heart disease (CHD), stroke, and total mortality. SNP rs1333049 (9p21.3) was associated with both CHD (HR=1.20, 95% CI 1.08-1.34) and stroke, rs11670734 (19q12) with total mortality and stroke, and several SNPs associated with lipid levels and blood pressure.

Traits studied:Blood pressureCoronary heart diseaseHDL cholesterolMyocardial infarctionNon-HDL cholesterolStrokeTotal mortality
The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol
AssociationN=3,974Nilesh J. Samani et al.(2008)· Journal of Molecular Medicine

This genome-wide association study investigated whether seven CAD-associated loci affect coronary artery disease risk through traditional cardiovascular risk factors. The study found that rs599839, located near PSRC1 and CELSR2 on chromosome 1p13.3, showed a strong association with serum cholesterol levels, with the risk allele A associated with 0.17 mmol/l higher total cholesterol per allele copy (P = 3.84 × 10⁻⁶) and 0.19 mmol/l higher LDL cholesterol (P = 8.56 × 10⁻⁵). This association was replicated in independent cohorts and the findings support further investigation of these genes in cholesterol metabolism and coronary risk.

Traits studied:Blood pressureBlood urateBody mass indexCoronary artery diseaseCreatinine clearanceGlucoseHDL cholesterolLDL cholesterolMyocardial infarctionTotal cholesterolWaist-hip ratio

About MIA3

Enables cargo receptor activity. Involved in several processes, including COPII-coated vesicle cargo loading; cell migration involved in sprouting angiogenesis; and regulation of leukocyte migration. Located in endoplasmic reticulum exit site and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all MIA3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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