rs261332
This is a coding sequence variant variant in the LIPC gene.
▶GWAS Catalog Trait Associations (16)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (16)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
low density lipoprotein cholesterol measurement
cholesteryl esters to total lipids in chylomicrons and extremely large VLDL percentage
high density lipoprotein cholesterol measurement
total lipids in small HDL measurement
triglyceride measurement, intermediate density lipoprotein measurement
total cholesterol measurement, blood VLDL cholesterol amount
cholesteryl ester measurement, blood VLDL cholesterol amount
triglyceride measurement
hematocrit
free cholesterol measurement, low density lipoprotein cholesterol measurement
About LIPC
Enables phospholipase A1 activity and triacylglycerol lipase activity. Involved in several processes, including cholesterol homeostasis; plasma lipoprotein particle remodeling; and triglyceride catabolic process. Located in extracellular space. Implicated in several diseases, including Alzheimer's disease; coronary artery disease; familial combined hyperlipidemia; peripheral vascular disease; and type 2 diabetes mellitus. Biomarker of hyperinsulinism; obesity; and type 1 diabetes mellitus. [provided by Alliance of Genome Resources, Jul 2025]
View all LIPC variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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