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Gene entry

LIPC

lipase C, hepatic type

Chromosome
15
Cytoband
15q21.3
Variants (rsID)
89

LIPC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q21.3). Its official name is “lipase C, hepatic type”. The reference table lists 89 variants (rsID) for this gene.

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Clinically classified variants

8 reference-table entries with clinical significance.

  • rs140272400Benignsingle nucleotide variantHyperlipidemia due to hepatic triglyceride lipase deficiency
  • rs2070895Benignsingle nucleotide variantHigh density lipoprotein cholesterol level quantitative trait locus 12|Diabetes mellitus type 2, susceptibility to
  • rs3829461Benignsingle nucleotide variantHyperlipidemia due to hepatic triglyceride lipase deficiency
  • rs3829462Benignsingle nucleotide variantHyperlipidemia due to hepatic triglyceride lipase deficiency
  • rs6083Benignsingle nucleotide variantHyperlipidemia due to hepatic triglyceride lipase deficiency
  • rs121912502Conflicting interpretationssingle nucleotide variantHyperlipidemia due to hepatic triglyceride lipase deficiency
  • rs8023503Othersingle nucleotide variant
  • rs182603751Uncertain significancesingle nucleotide variantHyperlipidemia due to hepatic triglyceride lipase deficiency

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.