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Gene entry

LPL

lipoprotein lipase

Chromosome
8
Cytoband
8p21.3
Variants (rsID)
30

LPL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8p21.3). Its official name is “lipoprotein lipase”. The reference table lists 30 variants (rsID) for this gene.

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Clinically classified variants

17 reference-table entries with clinical significance.

  • rs1059611Benignsingle nucleotide variantHyperlipoproteinemia, type I
  • rs11570892Benignsingle nucleotide variantHyperlipoproteinemia, type I
  • rs13702Benignsingle nucleotide variantHigh density lipoprotein cholesterol level quantitative trait locus 11|Hyperlipoproteinemia, type I
  • rs15285Benignsingle nucleotide variantHyperlipoproteinemia, type I
  • rs1801177Benignsingle nucleotide variantHyperlipidemia, familial combined, susceptibility to|Coronary heart disease|Hyperlipoproteinemia, type I
  • rs316Benignsingle nucleotide variantHyperlipoproteinemia, type I
  • rs326Benignsingle nucleotide variantHigh density lipoprotein cholesterol level quantitative trait locus 11
  • rs3735964Benignsingle nucleotide variantHyperlipoproteinemia, type I
  • rs118204057Conflicting interpretationssingle nucleotide variantHyperlipoproteinemia, type I|Hyperlipidemia, familial combined, LPL related|Hyperlipoproteinemia, type I|Hyperlipidemia, familial combined, LPL related
  • rs118204061Conflicting interpretationssingle nucleotide variantHyperlipoproteinemia, type I|Hyperlipidemia, familial combined, LPL related
  • rs268Conflicting interpretationssingle nucleotide variantHyperlipidemia, familial combined, LPL related|Hyperlipidemia, familial combined, susceptibility to|Hyperlipoproteinemia, type I
  • rs118204060Pathogenicsingle nucleotide variantHyperlipoproteinemia, type I|Hyperlipidemia, familial combined, LPL related
  • rs118204068Pathogenicsingle nucleotide variantHyperlipoproteinemia, type I
  • rs118204072Pathogenicsingle nucleotide variantHyperlipoproteinemia, type I
  • rs118204073Pathogenicsingle nucleotide variantHyperlipoproteinemia, type I
  • rs118204077Pathogenicsingle nucleotide variantHyperlipoproteinemia, type I
  • rs118204080Pathogenicsingle nucleotide variantHyperlipoproteinemia, type I

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.