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. Author manuscript; available in PMC: 2013 Nov 1.
Published in final edited form as: Clin Genet. 2012 Aug 7;82(5):408–415. doi: 10.1111/j.1399-0004.2012.01909.x

Appendix A.

Full text of genome sequencing knowledge items.

Sequencing limitations knowledge subscale
Once a variant in a gene that affects a person’s risk of a disease is found, that disease can always be prevented or cured.*
A health care provider can tell a person their exact chance of developing a disease based on the results from genome sequencing.*
Scientists know how all variants of genes will affect a person’s chances of developing diseases.*
Even if a person has a variant in a gene that affects their risk of a disease, they may not develop that disease.
Genome sequencing is a routine test that most people can have through their physician’s office.*
Sequencing benefits knowledge subscale
Genome sequencing may find variants in a person’s genes that they can pass on to their children.
Genome sequencing may give a person information about their chances of developing several different diseases.
Genome sequencing may find variants in a person’s genes that will increase their chance of developing a disease in their lifetime.
Genome sequencing may find variants in a person’s genes that will decrease their chance of developing a disease in their lifetime.
Genome sequencing may find variants in a person’s genes that may determine how they respond to certain medicines.
Additional item
A person’s health habits, like diet and exercise, can affect whether or not their genes cause diseases.
*

Note: These negatively worded items were reverse scored so that “strongly agree” reflected a correct response and “somewhat agree” reflected a less confident response in the correct direction for all items.