rs472495
This is a regulatory region variant variant in the PCSK9 gene.
▶GWAS Catalog Trait Associations (55)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (55)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
low density lipoprotein cholesterol measurement
apolipoprotein B measurement
total cholesterol measurement
proprotein convertase subtilisin/kexin type 9 measurement
cholesteryl ester measurement, blood VLDL cholesterol amount
free cholesterol measurement, low density lipoprotein cholesterol measurement
triglycerides in IDL measurement
free cholesterol measurement, intermediate density lipoprotein measurement
low density lipoprotein cholesterol measurement, phospholipid level
total cholesterol measurement, blood VLDL cholesterol amount
About PCSK9
This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an autocatalytic processing event with its prosegment in the ER and is constitutively secreted as an inactive protease into the extracellular matrix and trans-Golgi network. It is expressed in liver, intestine and kidney tissues and escorts specific receptors for lysosomal degradation. It plays a role in cholesterol and fatty acid metabolism. Mutations in this gene have been associated with autosomal dominant familial hypercholesterolemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]
View all PCSK9 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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