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rs2643826: Understanding Genetic Associations with Healthy Aging

rs2643826
Longevity & Healthspan
Moderate evidence

The genetic variant rs2643826 is an intergenic single nucleotide polymorphism (SNP) that has been identified in research studies exploring the genetic architecture of human longevity. It is currently categorized as a variant of interest in the study of healthy aging and age-related physiological traits.

What each genotype means

A/ALower attention

Associated with aging-related traits

This genotype is associated with research into healthy aging and lifespan-related traits. Because this variant is intergenic and identified through multivariate genomic scans, its specific biological mechanism remains under investigation and is not a direct predictor of individual longevity.

Specific population frequency data for this genotype is not currently recorded in major public databases.

A/GLower attention

Associated with aging-related traits

This genotype is associated with research into healthy aging and lifespan-related traits. Because this variant is intergenic and identified through multivariate genomic scans, its specific biological mechanism remains under investigation and is not a direct predictor of individual longevity.

Specific population frequency data for this genotype is not currently recorded in major public databases.

G/GLower attention

Associated with aging-related traits

This genotype is associated with research into healthy aging and lifespan-related traits. Because this variant is intergenic and identified through multivariate genomic scans, its specific biological mechanism remains under investigation and is not a direct predictor of individual longevity.

Specific population frequency data for this genotype is not currently recorded in major public databases.

What is rs2643826 and Where is it Located?

The variant rs2643826 is a single nucleotide polymorphism, which is a variation at a single position in the DNA sequence. This specific SNP is classified as intergenic, meaning it is located in the non-coding regions of the genome that lie between genes. Because it does not sit within a protein-coding gene, it is not responsible for creating a specific protein directly. Instead, researchers investigate intergenic variants like rs2643826 to determine if they play a role in regulating the expression of nearby genes or if they serve as markers for other functional genetic changes. In the context of complex traits like longevity, intergenic variants are frequently studied to understand how the non-coding genome influences biological processes over a human lifespan.

The Science of Longevity and Genetic Variation

Human longevity is a complex, polygenic trait, meaning it is influenced by the combined effects of many different genetic variants, each typically contributing a small effect size. Research into healthy aging often utilizes genome-wide association studies (GWAS) to compare the genetic profiles of long-lived individuals, such as centenarians, against control groups. While genes like APOE have been consistently replicated as major factors in longevity, many other variants, including rs2643826, are identified as potential contributors in specific study cohorts. It is important to note that the evidence for many longevity-associated SNPs remains moderate. Because aging is influenced by a combination of genetics, environment, and lifestyle, the presence of a specific variant does not guarantee a particular health outcome or lifespan.

Interpreting Research Findings

The association between rs2643826 and aging-related traits is based on statistical correlations observed in population-level research. In genomics, a lead SNP is a variant that shows the strongest statistical signal in a specific region during a GWAS. However, statistical association does not imply direct causation. Furthermore, genetic research often reveals that associations can be ancestry-specific; a variant that appears linked to a trait in one population may not show the same signal in another. Current research emphasizes that longevity is a multifaceted phenomenon. Readers should view these findings as part of an evolving scientific landscape rather than definitive medical predictors. As with all genetic information, these associations are intended for educational purposes and should not be used to make personal health decisions without consulting a qualified healthcare professional.

What You Can and Cannot Do with This Information

Understanding your genetic profile regarding variants like rs2643826 can be an interesting way to engage with the science of human biology. However, it is crucial to recognize the limitations of this data. You cannot use this information to diagnose a condition, predict your exact lifespan, or determine your future health status. Genetic variants associated with longevity are not diagnostic tools. If you are interested in your healthspan, the most effective approach remains focusing on well-established lifestyle factors, such as nutrition, physical activity, and regular medical screenings. If you have concerns about your health or family history, the best course of action is to discuss these topics with a doctor or a genetic counselor. They can provide context based on your complete medical history, which is far more informative than any single genetic variant.

How common is this variant?

There is currently no standardized population frequency data recorded for rs2643826 in major public databases, and its prevalence may vary significantly across different ancestral groups.

Frequently asked questions

Is rs2643826 a 'longevity gene'?

No, rs2643826 is not a gene; it is an intergenic SNP, meaning it is located in the DNA between genes. While it has been associated with longevity-related traits in some studies, it is not a single 'longevity gene' that determines lifespan.

Can I use this SNP to predict how long I will live?

No. Longevity is a complex trait influenced by thousands of genetic variants, environmental factors, and lifestyle choices. A single SNP like rs2643826 cannot predict an individual's lifespan.

Where can I find more information about this variant?

You can search for rs2643826 on the NCBI dbSNP database or the GWAS Catalog. These resources provide technical details and links to the original research studies where the variant was identified.

Should I be worried if I have a specific genotype for this SNP?

No. Genetic variants associated with complex traits like aging are typically identified through statistical associations in large groups, not as indicators of individual health risks. There is no reason to be concerned about your genotype for this variant.

Sources & further reading

Educational information only, last refreshed 10/3/2026. Not medical advice — these associations describe population statistics, not individual predictions.

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