Genetic Analysis Platform

Your DNA.
Decoded.

Upload your genetic data and receive comprehensive variant analysis, personalized health insights, and ancestry intelligence — powered by cutting-edge genomics science.

500K+
Variants Analyzed
98.7%
Accuracy Rate
24hr
Report Delivery
114
Gene Panels
Process

Intelligence in four steps.

From raw genetic data to actionable insight in under 24 hours.

01
📤
Upload Your Data
Submit your raw DNA file from any major testing provider — 23andMe, AncestryDNA, MyHeritage, or direct FASTQ/VCF.
02
🔬
Deep Analysis
Our pipeline cross-references your variants against curated scientific databases — ClinVar, OMIM, gnomAD, and more.
03
📊
Tiered Reporting
Receive a structured report organized by clinical significance — Guideline, Moderate, Emerging, and Research findings.
04
💡
Actionable Insights
Plain-language explanations of every finding, with research citations, population frequencies, and recommended follow-ups.
What We Analyze

Complete genomic intelligence.

Geneius covers the full spectrum of genetic analysis — from single nucleotide variants to complex trait prediction.

🧬
SNP Variant Analysis
Identification and classification of single nucleotide polymorphisms with clinical significance scoring and population frequency data.
Core Analysis
🏥
Health Risk Profiling
Evidence-based assessment of genetic predispositions for cardiovascular, metabolic, oncological, and neurological conditions.
Health
💊
Pharmacogenomics
Drug response predictions based on your genetic profile — identify optimal dosing, contraindications, and metabolism patterns.
Pharmacogenomics
🌍
Ancestry Composition
Deep ancestry analysis spanning 2,000+ geographic reference populations with haplogroup mapping and migration routes.
Ancestry
👨‍👩‍👧
Hereditary Traits
Inherited trait analysis covering physical characteristics, sensory traits, nutritional metabolism, and athletic predispositions.
Traits
🔗
Variant Pathways
Biological pathway mapping that connects your variants to upstream and downstream molecular processes and gene networks.
Advanced
Live Demo

See it in action.

Upload your raw DNA file and receive a full variant report in under 24 hours. All data is encrypted end-to-end.

Your genetic data never leaves our secure infrastructure. We process, analyze, and return your results — then permanently delete your raw file.

  • ✓ 256-bit AES encryption at rest
  • ✓ Zero third-party data sharing
  • ✓ HIPAA-compliant infrastructure
  • ✓ Raw file deleted post-analysis
🧬
Drop your DNA file here
or click to browse
TXT CSV VCF FASTQ 23andMe
Sample Report Preview
BRCA2 rs1799944Low Risk
APOE ε4 alleleModerate
CYP2D6*4Pharmacogen.
MTHFR C677TEmerging
HFE C282YGuideline
Access

Choose your level of insight.

From essential variant screening to comprehensive clinical-grade genomic intelligence.

Essential
$49/report
One-time analysis for individuals exploring their genetic profile.
  • SNP variant report (500+ variants)
  • Health risk summary
  • Ancestry composition
  • PDF report download
  • 30-day data access
Professional
$129/report
Full clinical-grade analysis with pharmacogenomics and pathway mapping.
  • Everything in Essential
  • Pharmacogenomics panel
  • Full pathway analysis
  • Interactive web dashboard
  • Clinical citations included
  • 1-year data retention
Enterprise
Custom
For clinics, research institutions, and corporate wellness programs.
  • Volume pricing
  • API integration
  • White-label reporting
  • HIPAA BAA included
  • Dedicated support
  • Custom gene panels
Get Started

Ready to decode your DNA?

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No spam. No data sharing. Cancel anytime.