23andMe raw DNA interpretation
Interpret your 23andMe raw DNA file in a readable report.
GenoSight interprets the raw genotype export from your existing 23andMe account and turns it into plain-language educational reports with source context, uncertainty, and clear medical boundaries.
Use the raw export
Use the raw genotype download from your 23andMe account.
What GenoSight does with your 23andMe file
The goal is to make a raw genotype file understandable without pretending it is a clinical test. GenoSight prioritizes findings, explains uncertainty, and keeps the report readable.
Prioritized variant context
Instead of making you scan a raw SNP table, GenoSight groups supported findings into readable sections with plain-language summaries.
Useful report domains
Explore educational context across nutrition, traits, fitness, pharmacogenomics, ClinVar-style health flags, and carrier-status context where coverage allows.
Health report path
If you are specifically looking for a 23andMe health report from raw data, start with the provider health-report guide and keep official 23andMe reports separate from GenoSight educational reports.
Caveats up front
Reports call out missing coverage, consumer-chip limits, and why a raw 23andMe file is not clinical confirmation.
Before you upload
23andMe provides raw data through its raw-data tool or account settings, then emails when the download is ready. Use that raw genotype file, not a PDF report or screenshot.
The 23andMe raw file is usually a zipped text file, often with a filename that begins with genome.
23andMe says raw data is informational and is not for medical, diagnostic, or clinical use. GenoSight keeps that same boundary.
If the download arrives as a zip file, keep the original private and upload the compatible raw genotype file when GenoSight asks for it.
Raw file parsing
GenoSight parses the genotype file first, checks provider format, and derives structured findings before report synthesis.
LLM boundary
The raw genotype file is not sent to the LLM. Report synthesis uses structured findings and your profile context.
Privacy stance
Files are stored under your account with encryption at rest, and GenoSight does not sell genetic data.
Pricing path
Start with the free report path, then upgrade only if it helps.
A provider-specific raw DNA file should earn trust with a real output first. Paid plans add more credits, PDFs, and report-grounded follow-up when the first report is worth continuing.
Free trial
$0
250 signup credits, no card
Run a real starter report from the provider file before deciding whether to pay.
Start freeMonthly
Popular$11.99
1,500 credits per month
Continue with more reports and findings-grounded follow-up chat after the first useful result.
Choose monthlyYearly
$99.99
18,000 credits per year
Best fit when you want broader coverage, PDFs, regenerations, and longer follow-up over time.
Choose yearlyLifetime
$229
6,000 credits per month, for life
For revisiting the same raw DNA file and future report updates without renewals.
Choose lifetimeFAQ
Can GenoSight interpret my 23andMe raw DNA data?
Yes. GenoSight is built to interpret and analyze compatible 23andMe raw genotype files. It does not interpret 23andMe PDF reports, ancestry screenshots, FASTQ, BAM, or whole-genome VCF files.
Do I need to buy another DNA test?
No. If you already have a compatible 23andMe raw data download, you can upload that file to GenoSight.
Is this medical advice?
No. GenoSight provides educational reports only. Consumer raw DNA data can have chip-coverage gaps and raw-call issues, so medical decisions require confirmation through a qualified healthcare professional. GenoSight reports are separate from official 23andMe health reports.
Can I try it before paying?
Yes. New accounts receive 250 free credits with no card required, enough to preview the report style before choosing a paid plan.