rs1433099

Variant in the LDLR gene (Low Density Lipoprotein Receptor)

rs1433099 is a single nucleotide polymorphism (SNP) in the LDLR gene, involved in cholesterol uptake. Variants at this position have been studied in relation to immune function, metabolism, and chronic illness.

This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.

What is the rs1433099 variant?

rs1433099 is a SNP (single nucleotide polymorphism) in the LDLR (Low Density Lipoprotein Receptor) gene. It belongs to the Lipid Metabolism category and is part of the Lipid Metabolism biological cluster. LDLR encodes the LDL receptor responsible for clearing LDL cholesterol from the bloodstream via receptor-mediated endocytosis.

Biological role and pathway

This variant sits within the LDLR gene, which is involved in the cholesterol uptake pathway. Genes within the Lipid Metabolism cluster work together to maintain balanced function across interconnected biological systems.

Variants in genes within this pathway may influence an individual's predisposition to altered function — particularly under conditions of physiological stress such as viral infection or prolonged illness.

rs1433099 and Long COVID / ME-CFS research

LDLR variants affecting cholesterol metabolism may influence vascular health and immune cell membrane composition relevant to Long COVID cardiovascular symptoms.

This information is based on published research and does not constitute medical advice. See references below.

Parent gene: LDLR

rs1433099 is one of 2 known variants in the LDLR gene. To understand the full biological context of this variant, explore the parent gene page.

View LDLR gene page →

Conditions studied in relation to rs1433099

Research into LDLR variants including rs1433099 has explored associations with the following conditions. These are areas of scientific investigation and do not imply causation.

Genetic insights from DNA data

Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include LDLR and the rs1433099 variant.

The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.

Other variants in the LDLR gene

The following variants in LDLR are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs1433099 variant in the LDLR gene?

rs1433099 is a single nucleotide polymorphism (SNP) located in the LDLR (Low Density Lipoprotein Receptor) gene, which is involved in cholesterol uptake. LDLR encodes the LDL receptor responsible for clearing LDL cholesterol from the bloodstream via receptor-mediated endocytosis.

How may the rs1433099 variant relate to Long COVID or ME/CFS?

LDLR variants affecting cholesterol metabolism may influence vascular health and immune cell membrane composition relevant to Long COVID cardiovascular symptoms.

Can a consumer DNA test detect the rs1433099 variant?

Many consumer DNA tests such as 23andMe, AncestryDNA, and MyHeritage genotype common SNPs. ChronicDNA analyses your raw DNA file and reports on variants studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.

Find out if you carry the rs1433099 variant

Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.

Get Your Personalised DNA Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for LDLR and its variants. This is not an exhaustive literature review.

  • [1]PMID: 33153018
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation