rs2376584

This is a intron variant variant in the PGS1 gene.

GWAS Catalog Trait Associations (7)

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

aspartate aminotransferase measurement

Allele A
OR 0.02
p 3.0e-23
N 928,679
Large GWAS
multi-ancestry
Allele A
OR 7.19
p 7.0e-13
N 389,565
Large GWAS
multi-ancestry

reticulocyte amount

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.02
p 8.0e-22
N 408,112
Large GWAS
European

reticulocyte count

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.02
p 6.0e-20
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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