How ReasonShield PGx Works

Get your personalized pharmacogenomics report in just a few simple steps. Our platform makes it easy to understand how your genes affect your medications.

1
Step One

Upload Your Genetic Data

Already have genetic data from 23andMe, AncestryDNA, or a clinical lab? Simply upload your VCF file to get started. If you don't have genetic data yet, we can help you get tested.

  • Accepts VCF files from any source
  • Compatible with consumer genetic tests
  • Works with clinical lab results

Drag & drop your VCF file

or click to browse

Processing...~2 minutes
Parsing VCF file
Identifying variants
Calling star alleles
Determining phenotypes
Generating recommendations
2
Step Two

AI-Powered Analysis

Our platform analyzes your genetic variants using clinically validated algorithms and reference databases including PharmVar, CPIC, and FDA guidelines.

  • Star allele calling for all 12 genes
  • Phenotype determination
  • Drug-gene interaction analysis
3
Step Three

Get Your Personalized Report

Receive a comprehensive report with your genetic results, drug recommendations, and actionable insights you can share with your healthcare provider.

  • Interactive web report
  • Downloadable PDF
  • Shareable wallet card

Your PGx Report

Ready
CYP2D6Intermediate Metabolizer
CYP2C19Normal Metabolizer
SLCO1B1Decreased Function

Dr. Smith

Primary Care Physician

“Based on your CYP2D6 intermediate metabolizer status, I'm adjusting your medication dosage to optimize effectiveness.”

4
Step Four

Consult With Your Provider

Share your results with your healthcare provider to make informed decisions about your medications. Your report includes clinical recommendations they can act on.

  • Provider-friendly clinical report
  • CPIC guideline references
  • Dosing recommendations

Ready to Get Started?

Upload your genetic data today and discover how your genes affect your medications.

Get Your PGx Report