SNOMED CT and FHIR have been used together in a genomics pilot in Queensland, Australia to assess the utility of collecting clinical phenotypic data from EHRs. The presentation provides the results of the pilot study. The results of which have been reviewed by clinicians for accuracy and quality, and provide a positive and useful exploration into how detailed clinical data can be extracted from EHRs to inform genomics research and future precision medicine endeavors. The pilot has created a FHIR value set of SNOMED CT content for phenotype findings, which can be used and further developed to provide a future data collection derivative. The pilot is important, as it provides a direct link for genomic researchers into granular data currently held within EHRs, which is currently difficult to access, but is essential to support future developments in the genomics area globally.