Raw DNA interpretation
Interpret your raw DNA file without pretending it is a diagnosis.
GenoSight turns compatible 23andMe, AncestryDNA, and MyHeritage raw DNA files into readable educational reports. Start with free credits, interpret one real report, then upgrade only if the output is useful enough to keep exploring.
Interpretation with boundaries
Useful context, plain limits.
- Educational genetic-health interpretation only, not diagnosis or treatment.
- Consumer raw DNA files can have missing calls, strand issues, and chip gaps.
- Raw genotype files are not sent to the LLM during report synthesis.
- GenoSight does not sell genetic data to advertisers, data brokers, or research partners.
Check the file first
Confirm that you have a raw genotype text export rather than a PDF report, screenshot, saved web page, FASTQ, BAM, or whole-genome VCF.
Check file formatPick one interpretation report
Start with the question you actually have: methylation, caffeine, sleep, heart, nutrition, fitness, APOE context, or a broader health report.
Pick a first reportAsk report-grounded follow-ups
Paid plans add chat tied to generated findings, so follow-up answers use report context rather than dumping raw genotype rows into a chatbot.
Compare plansWhat interpretation means
Separate raw marker lookup from health interpretation.
A raw DNA file is mostly rows of variant calls. Useful interpretation needs file compatibility checks, evidence context, and clinical limits, not just a long SNP table.
Marker lookup
A marker lookup answers whether a specific rsID appears in your file and what raw genotype string the file contains. It is not the same as a health interpretation.
Learn moreEducational report interpretation
GenoSight turns supported raw markers into readable reports with source context, caveats, and uncertainty, then keeps diagnosis and treatment decisions out of scope.
Learn moreClinical interpretation
Clinical interpretation requires validated testing, medical history, and a qualified professional. A consumer raw DNA file should not be used as clinical confirmation.
Learn moreReport starting points
Choose the first interpretation report by question.
The first report should answer a concrete question. After that, paid plans make more sense for deeper reports, PDFs, and longer follow-up chat.
Detox & Methylation
200 creditsInterpret MTHFR, COMT, folate, B-vitamin, and pathway context without claiming to measure methylation levels.
Foods & Drinks
160 creditsInterpret caffeine, alcohol, taste, and response patterns from supported markers in a practical, easy first report.
Sleep
100 creditsInterpret circadian, sleep-quality, and recovery-related educational signals when your raw file has usable marker coverage.
Mental Wellbeing
200 creditsInterpret mood, stress, sleep-mood, and resilience context while keeping diagnosis and treatment out of scope.
Fitness
100 creditsInterpret endurance, power, recovery, and training-response context while keeping athletic prediction claims out of scope.
Nutrition
350 creditsInterpret selected food, nutrient, and diet-related genetic context for people who want a broader health report.
Heart Health
200 creditsInterpret cardiovascular markers as educational context, with clear limits around diagnosis, treatment, and clinical confirmation.
Metabolic Health
160 creditsInterpret glucose, lipids, appetite, weight, and metabolic trait context while keeping labs and clinical care central.
Aging & Longevity
200 creditsInterpret APOE, inflammation, telomere, repair, and healthy-aging context without lifespan or dementia prediction.
APOE context
200 creditsInterpret sensitive APOE context cautiously, with counseling-aware boundaries and no standalone disease-risk promise.
Supported sources
Use the raw data export from the test you already took.
GenoSight is built for common consumer genotype files. If you are not sure what you downloaded, start with the local file checker before uploading anything to an account.
Compare raw DNA interpretation tools23andMe raw DNA interpretation
Use the downloaded raw genotype data file, not the 23andMe PDF or report screens.
AncestryDNA raw data interpretation
Use the AncestryDNA raw data download and expect chip coverage to vary by test version.
MyHeritage raw DNA interpretation
Use the MyHeritage raw DNA data export and keep provider-specific formatting in mind.
Pricing path
Start free, then pay only if interpretation is useful.
The free grant is meant to give you a real first read, not a fake teaser. Paid plans unlock more report depth and findings-grounded follow-up.
Free trial
$0
250 signup credits, no card
Enough to interpret one deeper starter report or two lighter reports before choosing a paid plan.
Start freeMonthly
Popular$11.99
1,500 credits per month
For active exploration after your first interpretation report proves the format is useful.
Choose monthlyYearly
$99.99
18,000 credits per year
For broader report coverage, regenerations, PDFs, and longer follow-up chat over time.
Choose yearlyLifetime
$229
6,000 credits per month, for life
For people who expect to keep revisiting the same raw DNA file without renewals.
Choose lifetimeRaw DNA interpretation questions
Common questions before interpreting raw DNA data.
Can GenoSight interpret my raw DNA data?
Yes, if you have a compatible consumer raw genotype text file from 23andMe, AncestryDNA, or MyHeritage. GenoSight does not interpret PDF reports, screenshots, FASTQ, BAM, or whole-genome VCF files.
Is raw DNA interpretation the same as medical advice?
No. GenoSight provides educational genetic-health interpretation only. Medical decisions require clinical-grade confirmation and a qualified healthcare professional.
What should I interpret first?
Most people should start with the report picker, Detox & Methylation, Foods & Drinks, Sleep, Heart Health, or a sample report. The free signup grant lets you test a real report before paying.
Does GenoSight interpret APOE or MTHFR?
GenoSight can provide cautious educational context for supported MTHFR, COMT, caffeine, and APOE markers, but it avoids standalone disease-risk promises and supplement instructions.
No card required
Interpret the first report before you pay.
Upload a compatible raw DNA file, use the free credits, and decide from an actual report instead of a promise.