RT Journal Article SR Electronic T1 GP attitudes to and expectations for providing personal genomic risk information to the public: a qualitative study JF BJGP Open JO BJGP Open FD Royal College of General Practitioners SP bjgpopen18X101633 DO 10.3399/bjgpopen18X101633 VO 3 IS 1 A1 Amelia K Smit A1 Ainsley J Newson A1 Louise Keogh A1 Megan Best A1 Kate Dunlop A1 Kylie Vuong A1 Judy Kirk A1 Phyllis Butow A1 Lyndal Trevena A1 Anne E Cust YR 2019 UL http://bjgpopen.org/content/3/1/bjgpopen18X101633.abstract AB Background As part of a pilot randomised controlled trial examining the impact of personal melanoma genomic risk information on behavioural and psychosocial outcomes, GPs were sent a booklet containing their patient’s genomic risk of melanoma.Aim Using this booklet as an example of genomic risk information that might be offered on a population-level in the future, this study explored GP attitudes towards communicating genomic risk information and resources needed to support this process.Design & setting Semi-structured interviews were conducted with 22 Australian GPs.Method The interviews were recorded and transcribed, and data were analysed thematically.Results GPs in this sample believed that communicating genomic risk may become a responsibility within primary care and they recommended a shared decisionmaking approach to guide the testing process. Factors were identified that may influence how and when GPs communicate genomic risk information. GPs view genomics-based risk as one of many disease risk factors and feel that this type of information could be applied in practice in the context of overall risk assessment for diseases for which prevention and early detection strategies are available. They believe it is important to ensure that patients understand their genomic risk and do not experience long-term adverse psychological responses. GPs desire clinical practice guidelines that specify recommendations for genomic risk assessment and patient management, point-of-care resources, and risk prediction tools that include genomic and traditional risk factors.Conclusion These findings will inform the development of resources for preparing GPs to manage and implement genomic risk information in practice.