Skip to main content

Table 3 Participant preferences when seeking permission for sharing genomics data when patient is no longer able

From: Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia

 

Total N (%)

Do you think someone else should be able to give permission for researchers to access your anonymous genomic data from medical records if you are no longer able? (N = 1491, 99.80%)

No, only I can give permission

353 (23.7)

No, data freely available

496 (33.3)

Yes

642 (43.1)

If Yes, who would you prefer to give permission for your anonymous genomic data to be used in research on your behalf? (you can select multiple answers) (N = 642)

Family member

392 (61.1)

Nominated legal respresentative

294 (45.8)

Doctor

125 (19.5)

Human Research Ethics Committee (HREC)

121 (18.9)

Data governance

61 (9.5)