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- Grebe, Theresa A2
- Khushf, George2
- Bailey, Dawn1
- Best, Robert G1
- Brenman, Leslie Manace1
- Clayton, Ellen Wright1
- Evans, Barbara J1
- Fivecoat, Jaime1
- Fullerton, Stephanie M1
- Gonzales, Patrick R1
- Grody, Wayne W1
- Hagenkord, Jill1
- Huang, Samuel J1
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- Rabin-Havt, Sara Schonfeld1
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- Stewart, Douglas R1
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- Tayeh, Marwan K1
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- Williams, Marc S1
Keyword
- autonomy1
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- De-identified genetic information1
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- Health Insurance Portability and Accountability Act of 1996 (HIPAA)1
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ACMG Statements and Guidelines
These online statements and guidelines are definitive and may be cited using the digital object identifier (DOI). These recommendations are designed primarily as an educational resource for medical geneticists and other healthcare providers to help them provide quality medical genetics services; they should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. Please refer to the leading disclaimer in each document for more information.
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- ACMG Statement
The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in MedicineVol. 25Issue 3100342Published online: December 22, 2022- Marwan K. Tayeh
- Margaret Chen
- Stephanie M. Fullerton
- Patrick R. Gonzales
- Samuel J. Huang
- Lauren J. Massingham
- and others
Cited in Scopus: 0Individuals have a right to access certain information in their medical records as established under the Health Insurance Portability and Accountability Act of 1996 (HIPAA).1 The specific information to which individuals have access is called a designated record set (DRS), a legal term of art defined in the HIPAA Standards for Privacy of Individually Identifiable Health Information (Privacy Rule).2 The Privacy Rule is a federal medical privacy law that applies to most clinical laboratories operating in the United States. - ACMG Statement
Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in MedicineVol. 24Issue 3p509–511Published online: December 16, 2021- Robert G. Best
- George Khushf
- Sara Schonfeld Rabin-Havt
- Ellen Wright Clayton
- Theresa A. Grebe
- Jill Hagenkord
- and others
Cited in Scopus: 1Human genomic data linked to health records have become valuable in the quest to establish correlations between disease and genetic information. As a result, it has become increasingly common for patient genetic information obtained through clinical testing or other means to be de-identified and linked to health records for sale or transfer to a third party for research and development purposes (eg, novel drug targets, patient and provider tools for managing health care). Unlike many other elements within the de-identified data set, however, the patient’s genetic information in various forms (eg, DNA sequence, RNA sequence, aggregated variant data, optical mapping) may be sufficiently information-rich to permit reidentification of the patient using informatics tools in some cases and is considered by some to be inherently identifiable. - ACMG StatementOpen Archive
The interface of genomic information with the electronic health record: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG)
Genetics in MedicineVol. 22Issue 9p1431–1436Published in issue: September, 2020- Theresa A. Grebe
- George Khushf
- Margaret Chen
- Dawn Bailey
- Leslie Manace Brenman
- Marc S. Williams
- and others
Cited in Scopus: 21Disclaimer: This statement is designed primarily as an educational resource for medical geneticists and other clinicians to help them provide quality medical services. Adherence to this statement is completely voluntary and does not necessarily assure a successful medical outcome. This statement should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results. In determining the propriety of any specific procedure or test, the clinician should apply his or her own professional judgment to the specific clinical circumstances presented by the individual patient or specimen.
