01
Upload your raw DNA file
Bring the raw-data export you already have from Ancestry or 23andMe. Your report starts with your own genotypes—not a generic quiz.
Raw DNA research, clarified
Your raw DNA, finally explained.
Upload your Ancestry or 23andMe raw data and turn scattered SNPs into a clear, evidence-aware research report: what matters, what might matter, and what probably does not.
Educational research only. Not medical advice or diagnosis.
The Superior Genes standard
Clarity without certainty theater.
Evidence is labeled
Stronger associations are separated from early, mixed, or population-specific findings.
Context comes first
One genotype is never presented as destiny, diagnosis, or a reason to change treatment.
From file to findings
Follow the evidence, not the hype.
Superior Genes turns rows of A, C, G, and T into a research map you can actually navigate.
02
Search SNPs without decoding jargon
Look up rsIDs and see a plain-English summary of what the research suggests, where evidence is mixed, and what remains unknown.
03
Connect related pathways
Explore findings across hormones, methylation, metabolism, inflammation, medication response, detox pathways, and nutrients.
The useful distinction
What matters. What might matter. What probably doesn’t.
Start at your depth
Research without a costly consultation.
Begin with a focused guide, interpret your full file, or keep up with new SNP research as it develops.
Starter Guide
10 SNPs to check
Free
A practical introduction to finding genotypes and reading claims critically.
- 10 searchable rsIDs
- Plain-English context
- Research caveats included
Most complete
Complete Interpretation
Your DNA research map
$49 one time
A downloadable, organized interpretation of supported variants found in your uploaded raw-data file.
- Hormones and metabolism
- Methylation and nutrients
- Inflammation pathways
- Medication-response research
- Evidence-strength notes
- Searchable SNP references
Research Library
Keep exploring
$12/month
Ongoing access for people who want new reports and a growing research database.
- New SNP briefings
- Searchable research library
- Evidence updates
Product features and compatible variants may evolve as the research library grows.
Questions, answered plainly
Before you upload your file.
Your file already has a story
Stop scrolling past your own DNA.
Start with ten SNPs, learn how to read the evidence, and decide how deep you want to go.