Abstract
<jats:p>Pharmacogenomics (PGx) can improve safety and effectiveness of commonly dispensed medicines, but its value at the population level depends on how often clinically actionable PGx phenotypes co-occur with the medicines they affect. We assessed this co-occurrence in a cross-sectional analysis of Our Future Health (OFH), a new UK national biobank, by applying Pharmacogenomics Clinical Annotation Tool (PharmCAT v3.1.1) to imputed genotypes from 738,531 participants across 17 pharmacogenes with established PGx prescribing guidelines. Every participant had at least one actionable PGx phenotype, with a mean of 6.1 (SD 1.3). The number of actionable PGx phenotypes was similar across genetically inferred ancestry groups, although the pharmacogenes contributing to that count differed between groups. Using linked primary care dispensing records, 36.8% (95% CI 36.7-36.9) had been dispensed at least one medicine between April 2018 and June 2025 matched to a gene for which they carried an actionable PGx phenotype. Co-occurrence rose with age, ranging from 43.7% to 58.9% across ancestry groups among those aged ≥70 years. Participants carried an actionable PGx phenotype for a mean of 13.8 (SD 6.5) of the 33 medicines dispensed in English primary care with PGx prescribing guidance, of which a mean of 0.6 (SD 1.0) had been dispensed. Co-occurrence was concentrated in a few widely dispensed classes, principally proton-pump inhibitors and antidepressants acting through CYP2C19 and statins through SLCO1B1. These findings highlight opportunities to optimise treatment for a large proportion of patients receiving routine medications and identify where pre-emptive PGx testing could have the greatest clinical benefit.</jats:p>