Pharmacogenomics (PGx)

Pharmacogenomics (PGx) studies how inherited genetic variation affects an individual's response to medications. Our PGx panel is designed to help clinicians optimise drug selection and dosing, reduce adverse drug reactions (ADRs), and improve treatment outcomes.

~80%
Pharmacogenomics explains ~80% of variability in genes associated with drug safety & efficacy.
~30%
Reduction in ADR cases with PGx-guided prescribing (published studies).
~70%
Physicians modify therapy based on PGx results (survey evidence).

How it works

We extract DNA from a simple saliva or blood sample, genotype clinically validated variants, and generate a concise report that maps genotypes to medication guidance. The report highlights recommended dose changes, alternative medications, and known high-risk drug-gene interactions.

  • Sample: Blood or buccal swab
  • Turnaround: 5–9 working days (standard)
  • Method: Targeted genotyping / NGS for selected pharmacogenes
  • Report: Clinician-facing report with actionable guidance and literature references

Note: PGx is a tool to support clinical decision-making. Results must be interpreted alongside clinical factors.

PGx diagram
PGx Gene Panel (39 genes)
Pharmacokinetic (PK), Pharmacodynamic (PD) and related genes tested
CSV
# Gene Symbol Role (typical) Notes
1 PDYD Related / other
2 FV Pharmacodynamic (PD)
3 MTHFR Related / other
4 UGT1A10 Pharmacokinetic (PK)
5 UGT2B15 Pharmacokinetic (PK)
6 UGT2B7 Pharmacokinetic (PK)
7 ABCG2 Pharmacokinetic (PK)
8 GABRA6 Pharmacodynamic (PD)
9 GABRP Pharmacodynamic (PD)
10 DRD1 Pharmacodynamic (PD)
11 TPMT Pharmacodynamic (PD) Thiopurine metabolism.
12 HLA-A Pharmacodynamic (PD) HLA alleles can predict severe immune reactions to some drugs.
13 FLOT1 Related / other
14 HCP5 Related / other
15 KIF6 Related / other
16 OPRM1 Pharmacodynamic (PD)
17 ABCB1 Pharmacokinetic (PK)
18 CYP3A5 Pharmacokinetic (PK)
19 CYP3A4 Pharmacokinetic (PK)
20 OPRK1 Pharmacodynamic (PD)
21 DBH Related / other
22 CYP2C19 Pharmacokinetic (PK) Affects SSRIs, clopidogrel metabolism.
23 CYP2C9 Pharmacokinetic (PK)
24 CYP2C8 Pharmacokinetic (PK)
25 ADRA2A Related / other
26 DRD4 Pharmacodynamic (PD)
27 F2 Pharmacodynamic (PD)
28 ANKK1 Pharmacodynamic (PD)
29 GRIK4 Pharmacodynamic (PD)
30 SLCO1B1 Pharmacokinetic (PK) Statin-associated myopathy risk (simvastatin).
31 HTR2A Pharmacodynamic (PD)
32 CYP1A2 Pharmacokinetic (PK)
33 PRSS53 Pharmacodynamic (PD)
34 VKORC1 Pharmacokinetic (PK) Warfarin sensitivity locus.
35 ITGB3 Pharmacodynamic (PD)
36 CYP2B6 Pharmacokinetic (PK)
37 APOE Pharmacodynamic (PD)
38 COMT Pharmacodynamic (PD) Modulates neurotransmitter catabolism; impacts response to some psych meds.
39 CYP2D6 Pharmacokinetic (PK) Well-known CYP affecting many antidepressants, opioids, antipsychotics.
Clinical utility
  • Helps personalise medication selection and dosing to reduce ADRs and improve efficacy.
  • Actionable guidance mapped to key drug–gene interactions used by clinicians across specialties.
  • Includes genes commonly cited in international guidelines; additional genes included for extended coverage.
Limitations
  • Not all rare variants or structural gene changes are tested; negative result does not rule out all genetic effects.
  • Drug response also depends on age, organ function, drug interactions and comorbidities — interpret in clinical context.
  • Genetic evidence evolves; we recommend periodic re-evaluation of variants and clinical recommendations.
Ordering & Sample

Sample: Blood or buccal swab

TAT: 5–9 working days

Price: Contact us for pricing

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