GLP-1 Genetic
Insights Tool

Explore what your genetics may mean for your GLP-1 journey.

  • See what research says about your GLP1R and GIPR variants
  • Learn about genetic factors studied in semaglutide and tirzepatide users
  • 100% private, runs entirely in your browser
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Genetic Insights

Based on Su et al., Nature 2026. Study of 27,885 GLP-1 users.

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Reading file…
🔒 100% private. Your genetic data never leaves your device. All analysis runs in your browser. Nothing is sent to any server.
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This tool is not medical advice, nor a thorough analysis of your data. It is not intended to treat, diagnose, or advise. This is an automated tool for informational purposes only, that exclusively looks for two specific single nucleotide polymorphisms (SNPs) in your genetic sequencing, not for any other risk factors, variants, or insights. AgelessRx is not responsible or liable for the accuracy of your genetic data or for how you may or may not use this tool and the results. If you want a more thorough review of your genetic data, please contact a genetic counselor. • This tool is based solely on findings from the study Su et al., Nature 2026. This study is very new and the findings have not yet been explored or duplicated by any other research team. The field of genetics is constantly evolving, and there are many factors that contribute to how an individual may respond to medication. • Using this tool does not create a clinician/patient or any other relationship. Your data is being processed on your own device, and is not being accessed by anyone else. It is deleted as soon as you close or refresh this site. • If you are an existing patient of AgelessRx, because your data and the results of this test do not leave your device, they will not be communicated to your provider. If you want your AgelessRx provider to know these results, please message them directly via your patient portal.
Your SNP Results
Two variants examined in the study for their association with GLP-1 medication experiences
GLP1R rs10305420
GIPR rs1800437
What the Research Suggests
Learn more about this tool

This tool is based on findings from Su et al., Nature 2026. For more context on how this tool works, its limitations, and clinical background, see the information on the landing page above.

This tool is not medical advice, nor a thorough analysis of your data. It is not intended to treat, diagnose, or advise. This is an automated tool for informational purposes only, that exclusively looks for two specific single nucleotide polymorphisms (SNPs) in your genetic sequencing, not for any other risk factors, variants, or insights. AgelessRx is not responsible or liable for the accuracy of your genetic data or for how you may or may not use this tool and the results. If you want a more thorough review of your genetic data, please contact a genetic counselor.

This tool is based solely on findings from the study Su et al., Nature 2026. This study is very new and the findings have not yet been explored or duplicated by any other research team. The field of genetics is constantly evolving, and there are many factors that contribute to how an individual may respond to medication.

Using this tool does not create a clinician/patient or any other relationship. Your data is being processed on your own device, and is not being accessed by anyone else. It is deleted as soon as you close or refresh this site.

If you are an existing patient of AgelessRx, because your data and the results of this test do not leave your device, they will not be communicated to your provider. If you want your AgelessRx provider to know these results, please message them directly via your patient portal.

How to Download Your Genetic Data

Don’t have your file yet? Here’s how to get it.

General Instructions
  1. Log in to your account on your genetic testing provider’s website
  2. Look for a “Download Raw Data”, “Download DNA Data”, or “My Files” section (usually in Settings or your account/data page)
  3. Download the raw data file. If multiple formats are available, choose VCF (.vcf) or the default raw data export (.txt or .csv)
  4. If the download is a .zip or .gz file, unzip it first
  5. Upload the resulting .txt, .csv, or .vcf file above
Compatible providers include: 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Nebula Genomics, Dante Labs, Sequencing.com, SelfDecode, and most other consumer or clinical genetic testing services that let you export your raw data.