Pharmacogenomic intelligence
for precision medicine

GeneOps provides pharmaceutical companies with a structured pharmacogenomics layer — covering drug-gene interactions, metabolic pathway variants, and adverse reaction risk profiles. Evidence-graded, continuously updated, and built for integration at scale.

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The pharmacogenomic
variants that matter most

The most clinically impactful pharmacogenomic variants — covering the metabolic pathways responsible for the majority of drug metabolism and the most common sources of adverse drug reactions.

CYP450 metabolizers

Phase I drug metabolism

CYP2D6, CYP2C19, CYP2C9, CYP3A4, and CYP1A2 — the enzymes responsible for metabolizing the majority of clinically used drugs. Poor, intermediate, extensive, and ultrarapid metabolizer phenotypes, with drug-specific implications.

Drug transporters

Uptake and efflux variation

SLCO1B1, ABCB1, and ABCG2 — transporter variants affecting bioavailability and tissue distribution of statins, antiretrovirals, and other transporter-sensitive compounds. Adverse reaction risk stratified by variant.

Coagulation and bleeding

Anticoagulant sensitivity

VKORC1 and CYP2C9 — the primary determinants of warfarin sensitivity and dosing. Extended to include NOACs and antiplatelet pharmacogenomics where evidence supports actionable guidance.

Receptor genetics

Target variability and response

OPRM1 opioid receptor variation, ADRB1/ADRB2 beta-adrenergic receptor polymorphisms, and dopamine receptor variants — affecting drug efficacy and dose-response relationships in the target population.

Phase II enzymes

Conjugation and clearance

NAT2 acetylation status, TPMT thiopurine metabolism, UGT1A1 glucuronidation — relevant to oncology, immunosuppression, and psychiatric pharmacogenomics.

Adverse reaction markers

HLA-associated hypersensitivity

HLA-B*57:01 (abacavir), HLA-B*15:02 (carbamazepine), and other HLA alleles associated with severe cutaneous adverse reactions — the most actionable pharmacogenomic findings in clinical practice.

Where pharmacogenomics
creates commercial value

Patient stratification

Genomic segmentation for clinical trial design and post-market analysis. Identify the patient populations most likely to respond, those at elevated adverse reaction risk, and the dosing windows that genomics predicts.

Companion diagnostic support

Structured pharmacogenomic data that supports companion diagnostic development — surfacing the variant profiles that correlate with efficacy or safety outcomes in your specific compound's mechanism of action.

Prescription decision support

An API layer that surfaces relevant pharmacogenomic findings at the point of prescribing — integrated into clinical workflows to flag metabolizer status, contraindications, and dosing considerations.

Label and evidence development

A structured, citation-traceable pharmacogenomics layer that supports label language development, prescribing information updates, and regulatory submission packages requiring genomic evidence.

Built to the standard
pharma requires

6,520+
Peer-reviewed papers, continuously updated
PubMed
Every finding links to primary citations
Graded
Confidence scoring on every variant-drug association
HGVS
Standard nomenclature and dbSNP cross-reference throughout

Pharmacogenomics
built for your program

We'll walk through the coverage relevant to your compound, the integration architecture, and the evidence standard our data is built to.

Request a Pharma Brief Medication Safety Use Case