PharmVar will serve as a central repository for pharmacogene variation to facilitate allele (haplotype) designation and the interpretation of pharmacogenetic test results to guide precision medicine.
PharmVar is a PGRN resource funded by NIGMS.
After September 26, 2017, please visit PharmVar.org to access content of the original P450 Nomenclature Database
We had a good turn out at the last PGRN-Wide Member Call on September 8th. Below are some key highlights from the call:
We will host our second PGRN-wide member call on Friday, September 8, 2017 at 11:00 am Pacific time via Webex (1:00 pm Eastern time). The agenda for the call can be found on the All-Members Calls page.
This call will feature an overview of two new PGRN resources: the Pharmacogenomics iPSC Library and Service (PiLS) by Nao Terada and Pharmacogene Variation Consortium (PharmVar) by Andrea Gaedigk.
We will conclude with an open discussion period during which you can bring up any item of interest.
Not yet a member? Apply for PGRN membership today by clicking here.
The Hub team