What is PharmGKB?
First time? Consider first taking a short guided clicking tour(opens in new window) through PharmGKB to get a feel for the website, and then quickly reading about how to search PharmGKB(opens in new window).
PharmGKB also has training exercises available to help new users find their way around the website. Note that these exercises are not to be used for credit, including professional development such as CME.
Download training exercises(opens in new window)Variant Annotations
Variant annotations are summaries of an association between a single genetic variant(opens in new window) and a drug response, as reported in a single publication. PharmGKB curators add these associations to the website when they come across them in published literature.
Scientists from around the world routinely publish articles showing how a particular genetic change affects how individuals respond to a drug(opens in new window), such as whether they have an adverse reaction or respond well. These articles are indexed on PubMed(opens in new window). PharmGKB curators use PubMed to find articles that contain pharmacogenomic(opens in new window) information then add that information to PharmGKB. PharmGKB uses an algorithm(opens in new window) to assess certain features of variant annotations and assign a score reflecting the combined attributes of a particular variant annotation. Variant annotation scores are used in the calculation of clinical annotation scores(opens in new window).
Interested in learning more?
- Walk me through a variant annotation(opens in new window)
- Read: More about variant annotations(opens in new window) by PharmGKB
- Read: PharmGKB as a clinical pharmacogenomic biomarker resource(opens in new window) by McDonagh et al.
- Read: An Evidence-Based Framework for Evaluating Pharmacogenomics Knowledge for Personalized Medicine(opens in new window) by Whirl-Carrillo, Huddart et al.