Baltimore et al recommend:
In the near term, we recommend that steps be taken to:
1) Strongly discourage, even in those 
countries with lax jurisdictions where it might be permitted, any 
attempts at germline
                     genome modification for clinical application in 
humans, while societal, environmental, and ethical implications of such 
activity
                     are discussed among scientific and governmental 
organizations. (In countries with a highly developed bioscience 
capacity,
                     germline genome modification in humans is currently
 illegal or tightly regulated.) This will enable pathways to responsible
                     uses of this technology, if any, to be identified. 
2) Create forums in which experts from 
the scientific and bioethics communities can provide information and 
education about
                     this new era of human biology, the issues 
accompanying the risks and rewards of using such powerful technology for
 a wide
                     variety of applications including the potential to 
treat or cure human genetic disease, and the attendant ethical, social,
                     and legal implications of genome modification. 
3) Encourage and support transparent 
research to evaluate the efficacy and specificity of CRISPR-Cas9 genome 
engineering technology
                     in human and nonhuman model systems relevant to its
 potential applications for germline gene therapy. Such research is 
essential
                     to inform deliberations about what clinical 
applications, if any, might in the future be deemed permissible. 
Baltimore et al have a point. Not only can this be significant on a person by person basis but it also has the potential to be weaponiozed. The technology is out there, thousands are now proficient in it, the cost is low and the means for distribution is high.
Clearly a sensible effort in collaboration with others is essential. The problem is that with much of science, the genie is out of the box.
 

 
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