3x4 Genetics delivers comprehensive nutrigenomics testing that analyzes 36+ genetic pathways — revealing how each patient's DNA influences nutrition, metabolism, detoxification, and performance. Personalized protocols backed by science.

3x4 Genetics goes beyond raw data. Their systems biology approach reveals how genes interact across multiple pathways — giving practitioners the insights needed to build truly personalized protocols.
Comprehensive analysis spanning methylation, detoxification, inflammation, cardiovascular, hormones, and athletic performance pathways.
Patient-friendly reports with clear dietary and supplement recommendations. Color-coded impact scores make complex genetics accessible.
Detailed MTHFR, COMT, CBS, and related SNP analysis for targeted B-vitamin, folate, and methylation support protocols.
Assess genetic predispositions for lipid metabolism, blood pressure regulation, homocysteine, and cardiovascular inflammation.
Evaluate genetic variants affecting neurotransmitter metabolism, cognitive function, mood regulation, and stress response.
Identify genetic factors for muscle fiber type, VO2 max potential, recovery speed, injury risk, and optimal training modalities.
A simple saliva sample unlocks a comprehensive genetic blueprint. No blood draw, no clinic visit required — just actionable insights delivered to your practitioner dashboard.

Practitioner orders a 3x4 Genetics test kit directly from the Omni Genomix dashboard. Ships to patient or clinic.
Patient provides a simple saliva sample at home or in-office. Non-invasive, painless, and takes under 2 minutes.
Sample is analyzed across 36+ genetic pathways in a CLIA-certified laboratory. Results in 2-3 weeks.
Comprehensive genetic report delivered to practitioner dashboard with clinical annotations and personalized protocol recommendations.
Most genetic tests look at genes in isolation. 3x4 Genetics uses a systems biology approach that reveals how genes interact across pathways — uncovering compound effects that single-gene tests completely miss.
Unlike single-gene tests, 3x4 analyzes how genes interact across multiple biological systems — revealing the full picture of how genetics influence health outcomes.
Natively integrated with the Omni Genomix ecosystem. Genetic results flow directly into practitioner dashboards, treatment protocols, and patient portals.
All samples processed in CLIA-certified, CAP-accredited laboratories. Rigorous quality control ensures accurate, reproducible results every time.
Reports go beyond raw data. Each pathway includes evidence-based dietary, supplement, and lifestyle recommendations practitioners can implement immediately.
Backed by a world-class scientific advisory board including geneticists, nutrigenomics researchers, and functional medicine pioneers.
Earn 25-35% margins on every test kit. Nutrigenomics creates recurring patient engagement through follow-up consultations and protocol adjustments.
"3x4 Genetics through Omni Genomix has transformed how I practice. I can now offer truly personalized nutrition protocols backed by each patient's unique genetic blueprint."
"The reports are incredibly detailed yet easy to explain to patients. The methylation and detox pathway analysis alone has changed outcomes for dozens of my chronic fatigue patients."
"Finally, a genetics test that gives me actionable data I can use in my nutrition practice. My patients love seeing the science behind their personalized protocols."
Every component of the 3x4 platform is designed for practitioner success — from test ordering to patient education and protocol building.
Comprehensive genetic test analyzing 36+ pathways across nutrition, metabolism, detoxification, inflammation, cardiovascular health, and athletic performance.
Color-coded genetic reports with clinical annotations, evidence-based recommendations, and patient-friendly summaries for consultation use.
Online platform where practitioners manage test orders, view results, build protocols, and track patient genetic profiles across their entire practice.
Unique visualization showing how genetic variants interact across multiple systems — revealing compound effects that single-gene tests miss entirely.
Each genetic finding is linked to peer-reviewed research, clinical guidelines, and evidence-based intervention recommendations for practitioner confidence.
White-labeled patient portal where patients can explore their genetic results, understand their pathways, and follow practitioner-assigned protocols.
3x4 Genetics is natively integrated with the full Omni Genomix ecosystem — from specimen collection through AI-powered automation.
See how practitioners across the country are transforming their practices with 3x4 Genetics — measured in revenue, efficiency, and patient outcomes.
ND, CGP — Clinical Genomics
Spending 2+ hours per patient interpreting raw genetic reports from other providers. Couldn't scale beyond 4 patients/day because genomic interpretation was the bottleneck. Patients received 50-page reports they couldn't understand.
Switched to 3x4 Genetics 36-pathway blueprint with pre-interpreted clinical recommendations. Integrated with Omni Genomix supplement protocols for automated personalized recommendations.
Interpretation Time
-96% time saved
Daily Patient Capacity
+200% throughput
Patient Compliance
+160% adherence
Genomic Revenue
+157% growth
"I went from spending 2 hours interpreting each genetic report to 5 minutes reviewing the 3x4 blueprint. The 36-pathway organization makes it immediately actionable. My patients actually understand their results now, and compliance with genetic recommendations went from 30% to 78% because the action items are clear."
— Dr. Natalie Brooks, ND, CGP — Clinical Genomics
MD, PharmD — Pharmacogenomics
12% of patients experienced adverse drug reactions due to undetected CYP450 variants. Each ADR cost an average of $4,200 in emergency care and follow-up. Existing PGx tests provided data but no clinical decision support at the point of prescribing.
Deployed 3x4 Genetics with real-time drug-gene interaction alerts integrated into PrymDx LIMS. Pharmacogenomic flags appear automatically before prescriptions are written, with alternative medication suggestions.
Adverse Drug Reactions
-87% ADRs
Emergency Costs Avoided
$394K/year saved
Prescribing Confidence
+54% confidence
Medication Efficacy
+44% first-try success
"We prevented 47 potential adverse drug reactions in the first 6 months — that's $197K in avoided emergency costs and immeasurable patient suffering prevented. The real-time alerts at the point of prescribing changed everything. I no longer have to remember which patients have which variants."
— Dr. William Chang, MD, PharmD — Pharmacogenomics
Most genetic tests produce overwhelming reports that practitioners can't interpret or act on. 3x4 Genetics translates DNA into specific, personalized clinical protocols.
Genetic reports are 50+ pages of raw data that practitioners don't have time to interpret
36-pathway blueprint organizing genetic variants into actionable clinical categories with prioritized intervention recommendations
5-minute interpretation time vs. 2+ hours for raw genetic reports
Nutrigenomics insights are disconnected from supplement and treatment protocols
Direct integration with Omni Genomix ecosystem — genetic findings automatically inform supplement recommendations, dosing, and treatment selection
Personalized protocols generated automatically from genetic data
Pharmacogenomic data isn't available when practitioners prescribe medications
Real-time drug-gene interaction alerts integrated into PrymDx LIMS, flagging metabolism variants before prescriptions are written
Prevent adverse drug reactions before they happen
Patients receive genetic results but don't understand what to do with them
Patient-facing genetic blueprint with plain-language explanations, personalized action items, and progress tracking as they implement changes
78% of patients actively implement genetic recommendations
One-time genetic tests provide no ongoing value after the initial consultation
Dynamic genetic insights that evolve — as new research emerges, patient reports automatically update with new actionable findings
Lifetime value from a single genetic test, not a one-time report
Practitioners can't correlate genetic predispositions with actual biomarker data
Gene-biomarker correlation engine connecting 3x4 genetic pathways with PrymDx lab results to show which genetic risks are actively expressing
Identify which genetic risks need immediate intervention vs. monitoring
Every partner in the Omni Genomix ecosystem is connected. Data flows seamlessly between layers — no silos, no manual handoffs.
Data Transferred
Saliva/blood specimen
Collection metadata
Patient consent
Requisition data
Data Transferred
Hormone panels
Metabolic markers
Inflammation markers
Thyroid function

3x4 Genetics
CurrentData Transferred
36-pathway analysis
SNP variant data
Gene-nutrient maps
Epigenetic markers

GetLabs

PRYM Wellness

3x4 Genetics
Current
PrymDx LIMS

Join the Omni Genomix ecosystem and offer your patients the most comprehensive genetic testing available. Start earning 25-35% margins on every test kit.