Golden Lotus Labs · ProxiGene™
Stop guessing.
Start sequencing.
Two patients on the same GLP-1 or peptide protocol can respond in opposite directions — because their genetics, not your dosing chart, decide how they metabolize it. ProxiGene reads 400+ validated biomarkers from a saliva sample and hands your practice a protocol built on one patient’s actual biology.
Free 52-page sample report. For licensed clinicians, med spas & wellness practices. Non-invasive · CLIA-certified lab · 3-week turnaround.
The Problem
Population-average protocols are costing you outcomes — and patients.
Every clinic dosing peptides or GLP-1s today is running on averages: the same starting dose, the same titration schedule, the same supplement stack for every patient who walks in. When a patient plateaus or reacts poorly, the assumption is compliance. Often, it’s genetics.
Standard Protocol
- –One dosing schedule for every patient
- –Adjustments made by trial and error
- –Non-responders assumed non-compliant
- –Supplement stack is generic, not personal
- –No visibility into metabolism variants
ProxiGene-Informed Protocol
- +Dosing informed by receptor sensitivity data
- +Risk flagged before the first prescription
- +Non-response explained by genetic variant
- +Peptide & supplement guidance is patient-specific
- +Follow-up labs targeted to real risk areas
What It Measures
400+ SNPs, organized into six clinical categories
Cognitive Degeneration
Memory pathways, neuroinflammation markers, and long-term cognitive decline risk.
Longevity
Inflammatory response, telomerase function, and cellular repair capacity.
Psychological Resilience
Neurotransmitter pathways tied to brain fog, anxiety, and stress response.
Micronutrient Metabolism
B9/B12 deficiency risk and methylation efficiency.
Metabolism & Energy
Cholesterol, triglycerides, and blood glucose regulation variants.
Food Sensitivity
Lactose intolerance and gluten sensitivity markers.
The Report
One report, five things your protocol can act on immediately
Delivered within three weeks of sample collection — built for the exam room, not a research paper.
Genetic Risk Matrix
Color-coded High / Medium / Low snapshot across 15 core biomarkers — readable in one glance before an appointment.
Gene & SNP Detail
rsID-level data with allele impacts, for clinicians who want to see the underlying variant.
Peptide & Supplement Guidance
Physician-curated protocol recommendations mapped to each patient's findings.
Nutrition & Lifestyle Insights
Evidence-based recommendations tied directly to the genetic findings, not generic advice.
Follow-Up Lab Suggestions
Confirmatory and monitoring labs targeted to the risk areas the panel surfaced.
Inside the Report
Don’t take our word for it — read an actual report
Every page below is from a real, de-identified ProxiGene report. Download the full 52-page sample and see exactly what lands in your inbox three weeks after the swab.
Patient-ready cover
Branded, accession-tracked, and clean enough to hand a patient across the desk.
High / Medium / Low per trait
A risk gauge and a plain-language assessment for every trait — readable before an appointment.
Marker-level detail
Gene, rsID, and the patient’s actual genotype, color-coded, with what the variant means.
Recommendations, including peptide & supplement guidance
Each trait closes with physician-curated next steps — the bridge from a genotype to the protocol you actually put the patient on.
400+
Validated SNPs analyzed per panel
3 wks
Sample-to-report turnaround
CLIA
Certified lab partner analysis
6
Clinical categories assessed
Free Sample Report
See the full report before you order a single kit
Download the complete 52-page de-identified patient report — every trait, every marker, and the peptide and supplement guidance that comes with it. We’ll follow up to walk your practice through it.
ProxiGene™ provides genetic insights to inform protocol development. It is not a diagnostic tool and does not diagnose, treat, or prevent any medical condition.