Clinical-grade whole genome sequencing with an AI-powered health agent. Get the same sequencing used by leading research institutions — and actually understand what it means.
Starting at $199 · Free shipping · Results in 6-8 weeks
Why Level Genomics
Most genetic tests only read a tiny fraction of your DNA. We sequence all of it — and give you the raw data.
30x and 100x whole genome sequencing performed in CLIA-certified labs. The same technology used by top research hospitals.
Unlike microarray tests that sample <1% of your DNA, we decode your entire genome — all 6 billion base pairs.
We never sell, share, or monetize your genetic data. Period. Your genome stays under your control. Request permanent deletion at any time — we wipe everything, no questions asked.
Download your complete genomic data — VCF, BAM, and FASTQ files. No lock-in, no restrictions.
personal genomic research assistant
Backed by 10,000+ peer-reviewed clinical studies across 5 major open-access databases, your personal genomic research assistant scans your entire genome, cross-references the latest research, and delivers prioritized, citation-backed health insights — not generic wellness advice.
ClinVar is the National Institutes of Health's open database that aggregates information about genomic variants and their relationship to human health. It contains millions of submissions from clinical testing laboratories, research institutions, and expert panels worldwide — making it the gold standard for understanding which genetic variants are clinically significant.
Your personal genomic research assistant performs an exhaustive scan of your entire genome against ClinVar's current catalog of pathogenic and likely-pathogenic variants. This isn't a spot check — it's a comprehensive intersection that covers millions of records to surface findings that matter to your health.
Your entire genome is compared against ClinVar — the NIH's authoritative database of genomic variants and their clinical significance. We scan millions of records to flag pathogenic and likely-pathogenic variants in your DNA.
Every finding is validated against guideline-grade sources: CPIC pharmacogenomics guidelines, ACC/AHA risk frameworks, and major peer-reviewed meta-analyses. No internet health myths.
Drug interactions, disease risk, carrier status, pharmacogenomics, nutrition — ask questions in plain language and get answers personalized to your genome with cited sources.
As new research is published and ClinVar is updated, your insights evolve. Your genome is sequenced once but understood continuously.
Your report is organized into distinct sections — each finding classified by clinical significance (High, Moderate, Low, or Favorable) with cited sources.
Findings organized across 7 body systems — cardiovascular, metabolic & endocrine, hematology & coagulation, neurologic, gastrointestinal, immune, and musculoskeletal. Each finding classified by clinical significance.
Drug-gene interactions covering CYP2C19, CYP2D6, SLCO1B1, VKORC1, DPYD, TPMT, and more — each rated by confidence level with CPIC guideline references to inform medication decisions.
Your entire genome cross-referenced against ClinVar's database of clinically significant variants. Matches categorized as pathogenic, drug response, risk factor, or benign — with review status and confidence level.
Consolidated view of actionable risk factors and favorable genetic findings. Risk factors prioritized by clinical impact; favorable factors highlight where your genetics work in your favor.
This is a real example of output from your personal genomic research assistant. Your genome is scanned across body systems, cross-referenced against ClinVar, and analyzed for drug-gene interactions — producing a prioritized report with cited sources and suggested follow-up steps.
Extract & classify variants
Your genome is scanned for clinically relevant variants across cardio, metabolic, pharmacogenomic, and immune pathways.
Full ClinVar intersection
Every variant is checked against millions of ClinVar records to identify pathogenic and likely-pathogenic findings.
Validate against guidelines
Findings are cross-referenced with CPIC, ACC/AHA, and major meta-analyses. Population frequencies separate rare from common.
Prioritized report with next steps
Results are ranked as urgent, monitor, or informational — with specific follow-up recommendations and source citations.
Level Genomics does not provide medical advice. All findings should be discussed with your healthcare provider.
Genomic Health Report
Example output from Level personal genomic research assistant
Executive Summary
4.8M variants analyzed · 30x sequencing depth · 99.5% genome covered · 99.97% call accuracy
Simple Pricing
Both plans include complete whole genome sequencing and full raw data access. You can optionally add our Personal Genomic Research Assistant — first month free with any kit. No hidden fees.
30x Whole Genome Sequencing
Complete whole genome sequencing at clinical-grade depth. The best starting point for understanding your genetics.
Order Standard Kit100x Whole Genome Sequencing
The most thorough sequencing available to consumers. Ultra-high accuracy for detecting rare variants and mosaicism.
Order Precision KitOptional add-on — not billed automatically
Continuous access to your personal genomic research assistant, backed by 10,000+ peer-reviewed clinical studies across 5 major open-access clinical databases. Ask questions, get proactive insights, and stay current as new research emerges.
Included free for 1 month with any kit purchase above
Your data, your choice
Clinical databases powering the personal genomic research assistant
Variant-disease clinical significance
Drug-gene interaction guidelines
Pharmacogenomic annotations
Genome-wide association studies
Gene-disease validity curation
All databases are open-access and freely published by their respective institutions. Updated regularly.
| Feature | 30x Standard — $199 | 100x Precision — $699 |
|---|---|---|
| Genome coverageThe percentage of your total DNA that gets read. 100% means your entire genome is analyzed — not just selected spots. | 100% | 100% |
| Sequencing depthHow many times each position in your DNA is read. Higher depth means higher accuracy. 30x is clinical-grade; 100x catches extremely rare variants. | 30x | 100x |
| Data generated | ~100 GB | ~300 GB |
| Accuracy | High (clinical-grade) | Ultra-high |
| Decodes all ~20,000 genesYour genome contains roughly 20,000 protein-coding genes. We read all of them — most consumer DNA tests only sample a tiny fraction. | ||
| Raw data download (VCF)Variant Call Format — lists every position where your DNA differs from the reference genome. Used by researchers and genetic counselors. | ||
| Raw data download (BAM)Binary Alignment Map — your full sequencing reads aligned to the human reference genome. The most complete form of your sequencing data. | ||
| Raw data download (FASTQ)The raw, unprocessed output from the sequencing machine — every DNA read before any analysis. The rawest form of your genomic data. | ||
| Pharmacogenomics reportsShows how your genes affect the way you process medications. Identifies drugs that may need different doses or alternatives based on your DNA. | ||
| Carrier status screeningChecks if you carry gene variants for inherited conditions you could pass to children — even if you're healthy yourself. Important for family planning. | ||
| Identifies rare genetic variantsDetects uncommon DNA changes that may be linked to health conditions. Higher sequencing depth finds more rare variants with greater confidence. | Standard | Enhanced |
| Mosaicism detectionFinds genetic variants present in only some of your cells, not all. These can be missed at lower depth. Requires 100x sequencing to detect reliably. | ||
| Structural variant analysisDetects large-scale DNA changes — deleted, duplicated, or rearranged segments — that standard consumer DNA tests completely miss. | Basic | Comprehensive |
| Personal Genomic Research Assistant (1st Month) | Free | Free |
| Personal Genomic Research Assistant (Ongoing) | $9/mo or $89/yr | $9/mo or $89/yr |
Privacy & Data Ownership
We built Level Genomics on a simple principle: your genetic data belongs to you and only you.
Your genetic data is never sold, licensed, or shared with third parties. Not for research, not for pharma, not for anyone.
AES-256 encryption for stored data and TLS 1.3 for all transfers. Your genome is protected with the same standards used by banks.
Full VCF, BAM, and FASTQ files available for download at any time. Your data is yours — no lock-in.
Request complete deletion of your data at any time. We will remove all copies from our servers within 30 days.
Choose exactly what data to share and with whom. Grant and revoke access to healthcare providers on your terms.
Our infrastructure meets HIPAA requirements for the protection of health information. Your privacy is not optional.
How It Works
Choose 30x or 100x sequencing. We ship a saliva collection kit to your door with free shipping.
Collect a simple saliva sample at home and mail it back in the prepaid envelope. No blood draw needed.
In 6-8 weeks, access your complete genome, download your raw data, and start exploring with the AI health agent.
Join thousands of people taking control of their genetic health. Order your kit today and start exploring your genome.
Free shipping · Saliva-based · Results in 6-8 weeks