Genomapp: Raw DNA Analysis10.6.2 - App Store

Make sense of your DNA test data and discover what your genes can tell you. Genomapp is a specialized genetic reference tool that cross-references your information with public databases of scientific studies to present findings in a visual, intuitive way.

Have you taken a DNA test? Did you know your genome has a lot to say? Want to learn more about your DNA? It is easier than you think.

*** Compatible with Ancestry & 23andMe

If you already have a raw DNA data file from services like 23andMe, AncestryDNA, FTDNA, or MyHeritage, you can safely use it. Genomapp provides a personalized genetic exploration of your AncestryDNA or 23andMe results. Our tool quickly identifies thousands of genetic markers (SNPs) and shows health associations found in scientific evidence.

*** Privacy & Security (100% On-Device)

Protecting your privacy is our primary concern.
. Your data remains on your device.
. Genetic files are not stored on or uploaded to our servers.
. We do NOT share genetic data with third parties.

*** Ready to start?

Genomapp has a Demo mode. If you want to try the app or learn how it works, you can access a fully functional version for free.

*** What does Genomapp offer?

We offer 3 free reports and 3 premium reports:
. Complex Diseases: Literature on markers associated with multifactorial conditions (genetic and environmental factors).
. Inherited Conditions: Scientific records on markers related to diseases that are caused by mutations in a single gene.
. Pharmacological Compounds: Drug-marker associations found in peer-reviewed scientific studies.
. Genetic Traits: Characteristics or attributes expressed by your genes.
. Observable Signs: Understand markers related to physical signs.
. Blood Groups: Literature-relevant markers for transfusions or pregnancy.

*** Specialized genetic insights

. Methylation & MTHFR: Focused on metabolic health research, folate, and the MTHFR gene.
. Aging & Longevity: Explore the genetic markers mentioned in studies about aging mechanisms.

*** Certification

The app has been reviewed by the mHealth.cat Office (TIC Salut Social Foundation). This means that the quality of the content and the usefulness of the functions have been evaluated, meeting reliability requirements for health-related educational content.

*** Not diagnostic

Please note that Genomapp is a medical reference and educational tool. It is NOT for diagnostic use and does not provide medical advice or clinical decision support. Always consult your healthcare professional for any medical concerns.

*** Our database

Search our database of more than 9,500 conditions, 12,400 genes, and 180,000 genetic markers. Our tool facilitates access to research on a comprehensive list of conditions from scientific sources, including breast cancer, Alzheimer's, and Parkinson's. It also indexes literature for tumor suppressor genes such as BRCA, PTEN, and P53.

*** Easy to Understand

Genomapp displays your DNA markers in a friendly way. Export your personalized genetic reports to PDF for your personal research and records to take them anywhere.

*** Supported DNA Providers

We are constantly adding support for new providers. Currently, you can use files from 23andMe, AncestryDNA, FTDNA, MyHeritage, Genes for Good, LivingDNA, Geno 2.0, and other DTC genetic testing companies. Genomapp also supports VCF format files and specific schemes. (Note: VCF files from WES/WGS are currently not compatible).

Try Genomapp now and unlock your DNA analysis!

Version History + Minor bug fixes
+ General improvements 10.6.2 4d ago Which condition would you like to see featured next? Vote in the poll and help choose the next one. 10.6.1 Sep 17 Which condition would you like to see featured next? Vote in the poll and help choose the next one. 10.6.0 Sep 16 + Minor bugs fixed
+ General improvement 10.5.4 Aug 17 + Minor bug fixes

+ General improvements 10.5.3 Jul 8 + Minor bug fixes

+ General improvements 10.5.2 Jun 24 The Genomapp 2026 Data Update is officially LIVE.

This isn’t just a small patch; it’s a giant leap in our processing power.

We’ve added:

266,000+ new genetic markers

1,700 new genes

1,600 new conditions

400,000+ total associations to compare against your raw DNA data

What’s waiting for you:

- Updated Alzheimer’s information (APOE, PSEN1/2).
- Expanded BRCA & Lynch Syndrome markers.
- The famous MTHFR "Wellness" gene update.
- New Caffeine metabolism insights (CYP1A2).

Please note that reports are personalised. While the new disease database includes additional markers, genes and conditions, not all reports will be affected by these changes.

Your DNA hasn't changed, but our ability to explore it just did! 10.5.0 Jun 9 + Minor bug fixes

+ General improvements 10.4.7 May 15 + Minor bug fixes

+ General improvements 10.4.6 Apr 28 + Minor bug fixes

+ General improvements 10.4.5 Apr 17 + Minor bug fixes

+ General improvements 10.4.4 Mar 21 + Minor bug fixes

+ General improvements 10.4.3 Mar 5 Marfan Syndrome is next Featured Condition

We are continuing our 10th-anniversary celebrations, and thanks to the suggestions you have sent us, we have seen a lot of interest in connective tissue disorders. With that in mind, as part of our Featured Condition series, we have selected Marfan syndrome.

Learn more about how this condition could be relevant to you. 10.4.0 Feb 10 + Minor bug fixes

+ General improvements 10.2.41 Jan 29 + Minor bug fixes

+ General improvements 10.2.4 Jan 27 + Minor bug fixes

+ General improvements 10.2.0 12/04/2025 A decade decoding the future of your health

Genomapp celebrates 10 years of breakthroughs, insights, and empowerment.

To mark our ten-year anniversary, we're introducing the "Featured Condition" section, offering specialized content to help you better understand certain genetic conditions. We’re starting with Ehlers-Danlos syndrome. 10.0.2 11/03/2025 A decade decoding the future of your health

Genomapp celebrates 10 years of breakthroughs, insights, and empowerment.

To mark our ten-year anniversary, we're introducing the "Featured Condition" section, offering specialized content to help you better understand certain genetic conditions. We’re starting with Ehlers-Danlos syndrome. 10.0.1 10/26/2025 A decade decoding the future of your health

Genomapp celebrates 10 years of breakthroughs, insights, and empowerment.

To mark our ten-year anniversary, we're introducing the "Featured Condition" section, offering specialized content to help you better understand certain genetic conditions. We’re starting with Ehlers-Danlos syndrome. 10.0.0 10/24/2025 + Minor bug fixes

+ General improvements 9.4.5 10/11/2025 + Minor bug fixes

+ General improvements 9.4.3 10/06/2025 + Minor bug fixes

+ General improvements 9.4.2 09/26/2025 + Minor bug fixes

+ General improvements 9.4.1 09/13/2025 + Minor bug fixes

+ General improvements 9.4.0 09/03/2025 + New feature! You can now access a gene's marker list directly from its detail page. Give it a try!

+ Minor bug fixes

+ General improvements 9.3.0 07/24/2025