Mutant Genomics Educational DNA analysis

See the patterns in your DNA. Explore them in context.

Mutant looks across biological systems to surface ranked health hypotheses, with evidence and limitations in view. Explore the findings in the portal or connect them with symptoms, labs, and records in ChatGPT.

Gut & immuneClinical & inheritedMetabolismBrain & stress
View a Sample Analysis

No new DNA test required Educational hypotheses, not diagnoses

Connect Your DNA and Health Context in ChatGPT

Your genes are one part of the story. Explore them alongside the health details you choose to share.

Your DNA file → Mutant

Genetic findings

Ranked patterns, evidence, and limits

What you choose to share

Health context

Symptoms, labs, records, medications

ChatGPT
DNA meets your health story

Explore the connections.

Look at genetic findings alongside your symptoms, labs, and records—with the evidence and limits in view.

Example question“How might my DNA findings relate to these symptoms and lab results?”
Explore patterns, caveats, and better follow-up questions.

A deeper look at your DNA

Evo 2 is an AI model that learns patterns in DNA sequences.

Mutant uses its sequence-context scores to refine the weights of genetic variants already used in your analysis.

Learn how Evo 2 works in Mutant
DNA sequence analyzed by Evo 2 to adjust a variant's weight

Arc Institute developed Evo 2 as a 40-billion-parameter DNA model using genetic sequences from organisms across the tree of life.

Trained on more than 9 trillion nucleotides

Built for Responsible DNA Interpretation

See the evidence, coverage, and uncertainty behind each genetic hypothesis.

Your Raw Genome Stays on Your Device

Your genome file is processed locally in your browser and is never uploaded or stored by Mutant. Only the variants Mutant uses—currently about 600 SNPs—are uploaded and stored with your account.

Patterns, Not Isolated Variants

Findings are based on converging evidence across related variants, pathways, biological systems, and symptom context—not one variant considered in isolation.

Evidence and Coverage Are Visible

Research quality, biological relevance, and converging genetic signals shape each hypothesis. Mutant shows supporting evidence, missing coverage, and important limitations.

Hypotheses, Not Diagnoses

Genetic associations can suggest susceptibility, but they cannot establish a condition or cause. Mutant provides educational hypotheses, not diagnoses or treatment plans.

Learn how Mutant evaluates the evidence

Explore Your Biological Systems

Mutant groups related genetic findings so you can see where patterns converge.

Gut and immune system illustration

Gut, Barrier & Immune Reactivity

Explore how digestion, barrier function, and immune activity may connect.

Clinical and inherited health illustration

Clinical & Inherited Health

Review inherited patterns that may warrant closer clinical follow-up.

Metabolic system illustration

Metabolic Reactivity

See how nutrient handling, energy, and biochemical responses may overlap.

Brain and nervous system illustration

Stress, Mood & Neurochemical Regulation

Explore patterns in signaling, arousal, recovery, and sleep.

These are areas for exploration, not diagnoses.

Beyond the ChatGPT conversation

Explore Mutant in the Portal

Connect your DNA to the health context you share in ChatGPT, then use the Mutant portal to browse ranked findings, evidence, and limitations.

Try an Interactive Sample Analysis

See how Mutant turns genetic findings into an organized, explorable view.

  • Browse biological systems and focused hubs
  • Review ranked health hypotheses
  • Inspect the evidence, coverage, and limitations behind each result
Interactive sample analysis previewInteractive sampleExplore the Sample Analysis →

Start With the DNA Data You Already Have

No new DNA test is required. Start with a file from a test you have already taken; available findings depend on its source and version.

Quick start

Microarray DNA

Supported sources:

  • 23andMe raw data
  • AncestryDNA raw data

Covers many common variants Mutant evaluates. Coverage varies by provider and test version; missing data is shown clearly.

Broadest coverage

Whole-Genome Sequencing

Supported format:

  • VCF files containing SNPs and supported insertion/deletion variants

Typically offers the most complete coverage of variants Mutant evaluates, including some absent from consumer microarray files.

Your Raw Genome File Stays on Your Device

Your file is processed locally in your browser. Only the specific variants used in Mutant’s analysis are uploaded and stored with your account.

You can start with the data you have and add more complete genome data later.

A free account includes selected features. Unlock the complete Mutant experience for $49 per year. No credit card required to start.

Compare microarray and whole-genome sequencing coverage →

Your Genetics, Organized Into a Clearer Health Context

Mutant does not treat individual variants as answers. It organizes related genetic findings—and any health context you choose to provide—into structured patterns and ranked health hypotheses you can explore further.

Systems & Converging Patterns

See your variants organized into biological modules, systems, and focused hubs. Mutant also identifies converging patterns where multiple inherited tendencies overlap.

Ranked Health Hypotheses

Review the hypotheses with the strongest combined support from your available genetic data and optional health context. Each hypothesis explains why it was prioritized.

Evidence, Coverage & Limitations

Inspect supporting variants, evidence quality, genetic coverage, missing data, and important uncertainties behind each result.

Use Your Analysis Your Way

Review your results directly in Mutant. Access Mutant through its ChatGPT plugin to explore your findings alongside health information available in your conversation, or export your AI-ready Health Context for use with another compatible AI tool.

A free account includes selected features. Unlock the complete Mutant experience for $49 per year. No credit card required to start.

Mutant provides educational genetic analysis. Health hypotheses are possibilities to explore—not diagnoses or established causes.

Who Mutant Is Built For

For people who want a more organized, evidence-aware way to explore how genetics may fit into their broader health picture.

People Who Want More From Their DNA Data

If you already have raw DNA data, Mutant helps you move beyond ancestry, general wellness traits, and isolated variant reports by organizing related findings across pathways and biological systems.

People Exploring Complex Health Questions

When symptoms, laboratory results, and health history do not fit a simple explanation, Mutant surfaces ranked genetic health hypotheses that can be compared with other information and explored further.

People Using AI to Organize Their Health Information

If you use ChatGPT or another AI tool, Mutant provides structured genetic context you can explore alongside your medical records, labs, medications, symptoms, and health history.

© 2026 Mutant Biotech, Inc. All rights reserved. Mutant Genomics is a brand of Mutant Biotech.

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