rs58301047
This is a intron variant variant in the GPIHBP1 gene.
▶GWAS Catalog Trait Associations (17)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (17)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
phospholipids in large HDL measurement
HDL cholesterol change measurement
free cholesterol in HDL measurement
total lipids in large HDL
concentration of large HDL particles measurement
free cholesterol to total lipids in very large HDL percentage
HDL particle size
cholesterol in large HDL measurement
free cholesterol in large HDL measurement
phospholipids:total lipids ratio
About GPIHBP1
This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins. The encoded protein is a glycosylphosphatidylinositol-anchored protein that is a member of the lymphocyte antigen 6 (Ly6) family. This protein plays a major role in transporting lipoprotein lipase (LPL) from the subendothelial spaces to the capillary lumen. Mutations in this gene are the cause of hyperlipoproteinemia, type 1D. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]
View all GPIHBP1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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