One major concern that stands out to me is the privacy and security of genetic data. Our DNA is essentially the “ultimate personally identifying information” that can’t be changed if compromised.

As this sensitive data becomes digitized and stored in databases, it creates new cybersecurity risks – genetic information could potentially be hacked, stolen, or misused by cybercriminals. I believe robust security measures and strict privacy protections are crucial to safeguard this data.

Another key ethical consideration is the potential for misuse of CRISPR technology. Could it be used to create biological weapons or hack human DNA for malicious purposes? There are also risks of unintended consequences from gene editing. I think oversight and regulation are essential to prevent misuse while still allowing beneficial research.

Issues of equity and access are also important to consider. Will gene editing only be available to the wealthy, potentially increasing societal divides? How can we ensure fair access to potentially life-saving genetic therapies? I believe policies need to be developed to promote equitable access and prevent CRISPR from exacerbating existing inequalities.

The complexity of gene editing also raises challenges for informed consent. How can we ensure people fully understand the risks and implications before consenting to genetic modifications? What about editing embryos who cannot consent?  I would want to see robust informed consent processes emphasized in bioethics education.