@article{b5427ae586fa454fb522ae01a929a2ab,
title = "ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)",
keywords = "Exome sequencing, Genome sequencing, Incidental findings, Secondary findings",
author = "{ACMG Secondary Findings Working Group} and Miller, {David T.} and Kristy Lee and Abul-Husn, {Noura S.} and Amendola, {Laura M.} and Kyle Brothers and Chung, {Wendy K.} and Gollob, {Michael H.} and Gordon, {Adam S.} and Harrison, {Steven M.} and Hershberger, {Ray E.} and Klein, {Teri E.} and Richards, {C. Sue} and Stewart, {Douglas R.} and Martin, {Christa Lese}",
note = "Funding Information: Funding and support listed here did not support development of this document unless included in the Acknowledgments section. N.S.A.-H. is an equity holder of 23andMe; serves as a scientific advisory board member for Allelica; received personal fees from Genentech, Allelica, and 23andMe; received research funding from Akcea; and was previously employed by Regeneron Pharmaceuticals. W.K.C. is a member of the scientific advisory board of Regeneron Genetics Center. D.T.M. has received an honorarium from Ambry Genetics. D.R.S. is supported by the Intramural Research Program of the Division of Cancer Epidemiology and Genetics of the National Cancer Institute, Rockville, MD, and also performs contract clinical telehealth services for Genome Medical, Inc., in accordance with relevant National Cancer Institute ethics policies. All other authors declare no conflicts of interest.",
year = "2023",
month = aug,
doi = "10.1016/j.gim.2023.100866",
language = "English",
volume = "25",
journal = "Genetics in Medicine",
issn = "1098-3600",
number = "8",
}