rs12601079

This is a downstream gene variant variant in the PGS1 gene.

GWAS Catalog Trait Associations (9)

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

high density lipoprotein cholesterol measurement

Allele A
OR 0.03
p 8.0e-35
N 297,626
Major Consortium StudyLarge GWAS
multi-ancestry

triglycerides in IDL measurement

Allele G
OR 0.03
p 5.0e-16
N 199,732
Large GWAS
European

fatty acid amount

Allele G
OR
p 9.0e-15
N 239,268
Large GWAS
European

mean corpuscular hemoglobin concentration

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 0.02
p 6.0e-14
N 583,935
Major Consortium StudyLarge GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.01
p 1.0e-9
N 408,112
Large GWAS
European

About PGS1

Predicted to enable CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase activity and calcium ion binding activity. Predicted to be involved in cardiolipin biosynthetic process and diacylglycerol metabolic process. Located in endoplasmic reticulum. Is active in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

View all PGS1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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