AI-Powered Genomics

Unlock your health's future with
Polygenic Risk Scoring

Utilize advanced AI-driven analysis of your unique DNA sequence to uncover hidden genetic predispositions. Make informed, proactive decisions for your long-term wellness.

AI DNA Visualization
AI-Enhanced Analysis
Comprehensive DNA Sequencing
100% Data Privacy
Predictive Science

Beyond single genes: Understanding Polygenic Risk

Most common health conditions aren't caused by a single genetic mutation, but by the combined subtle effects of millions of variations across your genome. Our Polygenic Risk Score (PRS) technology analyzes these complex patterns.

  • Deep AI Processing: We utilize machine learning algorithms trained on massive genomic databases to calculate your precise risk percentiles for dozens of complex conditions.
  • Actionable Insights: A genetic predisposition is not a diagnosis. By identifying your baseline risks early, our clinicians can tailor lifestyle, nutritional, and medical interventions to keep you healthy.
  • Continuous Updates: As scientific understanding of the genome evolves, your digital PRS dashboard updates, giving you a lifelong companion in personalized medicine.
PRS Analysis Dashboard

Key Areas of Analysis

Cardiometabolic Health

Predispositions to elevated cholesterol, hypertension, and insulin resistance.

Neurocognitive & Wellness

Genetic markers linked to vitamin absorption, stress response, and cognitive longevity.

Your Genetic Journey

Discover your DNA in three simple steps

1

Saliva Collection

We mail a simple, painless at-home DNA collection kit. Provide a saliva sample and mail it back in the prepaid secure envelope.

2

Lab Sequencing & AI

Our CLIA-certified partner lab extracts your DNA, evaluating 13,000+ genomic variants and calibrating against global ancestries via the PGS Catalog.

3

Clinical Review

Review your secure report with risk percentiles and Z-scores. Tele-consultations provide customized preventative protocols.

Actual Clinical Report DataSample: NG17LJQJTEBuild: GRCh38

Polygenic Risk Score (PGRS) Clinical Results

Real computational output calculated by the PGS Catalog Calculator (pgsc_calc v2.0.0) across 2,576 reference genomes.

Catalog Accession
PGS001851 • GRCh38
Patient PercentileElevated Risk
71.7th %ile

Higher predisposition than 71.7% of ancestry-matched individuals.

Ancestry Z-Score (Z_MostSimilarPop)
+0.62 SD

+0.62 standard deviations from reference population mean.

Most Similar Population
AFR (100%)

Calibrated against 1000 Genomes Project (681 AFR samples).

Scored Effect Variants
8,810 / 13,855

63.6% high-confidence overlap across genome sequencing.

Adjusted Score Distributions (PGS001851_hmPOS_GRCh38)

Actual output from report.html comparing patient sample (pink) against the 1000 Genomes reference cohort (cyan).

PGS001851 Adjusted Distributions Density Plot
1. SUM
Raw additive polygenic score (0.167)
2. Z_MostSimilarPop
Ancestry standardized (0.62 SD)
3. Z_norm1
1st degree PCA adjustment (0.67 SD)
4. Z_norm2
2nd degree PCA adjustment (0.66 SD)
Analyzed Disease Condition

Gastroesophageal Reflux Disease & Esophagitis

Catalog Study: PGP000263
Scientific Citation:

"Privé F et al. Am J Hum Genet (2022). doi:10.1016/j.ajhg.2021.11.008"

What this 71.7% Percentile Means:

The patient carries above-average genetic variants linked to esophageal tissue inflammatory response. This is not a diagnosis of disease, but a valuable clinical roadmap for preventative care.

Recommended Preventative Action:
  • Alkaline and anti-inflammatory nutrition protocol.
  • Targeted digestive enzyme and mucosal barrier compounds.
  • Annual clinical telemetry check-in with medical provider.

Knowledge is the best medicine

Join thousands of patients taking proactive control of their health trajectory through the power of clinical-grade genetics.

Payment & Billing

Straightforward payment for every treatment

PrecisionMeDNA is a cash-pay practice across all services, which keeps your pricing clear and your care free of insurance-network restrictions. We don't bill insurance directly — but we make it easy to use the health funds you already have, and we give you everything you need to seek reimbursement on your own plan.

HSA & FSA accepted

Use your Health Savings or Flexible Spending Account toward any procedure, applied directly at the time of payment.

Cash-pay pricing

One clear price per service, paid at the time of care — no surprise network billing and no claims to chase first.

Reimbursement support

After your visit you'll receive an itemized superbill to submit to your insurer for possible out-of-network reimbursement.

The same terms apply to every service

HSA/FSA · Cash-pay · Superbill provided

Please note: PrecisionMeDNA is an out-of-network, cash-pay provider and does not submit claims to insurance carriers. A superbill is provided on request so you may seek reimbursement under your plan's out-of-network benefits. Reimbursement is determined solely by your insurer and is not guaranteed. HSA/FSA eligibility depends on your plan administrator's rules.