rs118039278
This is a intron variant variant in the LPA gene.
▶GWAS Catalog Trait Associations (26)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (26)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
lipoprotein A measurement
cholesteryl esters:total lipids ratio, blood VLDL cholesterol amount, chylomicron amount
cholesterol to total lipids in chylomicrons and extremely large VLDL percentage
free cholesterol to total lipids in chylomicrons and extremely large VLDL percentage
total lipids in chylomicrons and extremely large VLDL measurement
triglycerides in chylomicrons and extremely large VLDL measurement
cholesteryl esters to total lipids in chylomicrons and extremely large VLDL percentage
apolipoprotein B measurement
low density lipoprotein cholesterol measurement
triglycerides in HDL measurement
About LPA
The protein encoded by this gene is a serine proteinase that inhibits the activity of tissue-type plasminogen activator I. The encoded protein constitutes a substantial portion of lipoprotein(a) and is proteolytically cleaved, resulting in fragments that attach to atherosclerotic lesions and promote thrombogenesis. Elevated plasma levels of this protein are linked to atherosclerosis. Depending on the individual, the encoded protein contains 2-43 copies of kringle-type domains. The allele represented here contains 15 copies of the kringle-type repeats and corresponds to that found in the reference genome sequence. [provided by RefSeq, Dec 2009]
View all LPA variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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