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Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.
Webber, Elizabeth M; Hunter, Jessica Ezzell; Biesecker, Leslie G; Buchanan, Adam H; Clarke, Elizabeth V; Currey, Erin; Dagan-Rosenfeld, Orit; Lee, Kristy; Lindor, Noralane M; Martin, Christa Lese; Milosavljevic, Aleksandar; Mittendorf, Kathleen F; Muessig, Kristin R; O'Daniel, Julianne M; Patel, Ronak Y; Ramos, Erin M; Rego, Shannon; Slavotinek, Anne M; Sobriera, Nara Lygia M; Weaver, Meredith A; Williams, Marc S; Evans, James P; Goddard, Katrina A B.
Affiliation
  • Webber EM; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
  • Hunter JE; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
  • Biesecker LG; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Buchanan AH; Genomic Medicine Institute, Geisinger, Danville, Pennsylvania.
  • Clarke EV; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
  • Currey E; Division of Genomics and Society, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Dagan-Rosenfeld O; Department of Genetics, Stanford University, Stanford, California.
  • Lee K; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina.
  • Lindor NM; Department of Health Science Research, Mayo Clinic Arizona, Scottsdale, Arizona.
  • Martin CL; Autism & Developmental Medicine Institute, Geisinger, Danville, Pennsylvania.
  • Milosavljevic A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Mittendorf KF; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
  • Muessig KR; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
  • O'Daniel JM; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina.
  • Patel RY; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Ramos EM; Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
  • Rego S; Institute for Human Genetics, University of California, San Francisco, San Francisco, California.
  • Slavotinek AM; Department of Pediatrics, University of California, San Francisco, San Francisco, California.
  • Sobriera NLM; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Weaver MA; American College of Medical Genetics and Genomics, Bethesda, Maryland.
  • Williams MS; Genomic Medicine Institute, Geisinger, Danville, Pennsylvania.
  • Evans JP; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina.
  • Goddard KAB; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon.
Hum Mutat ; 39(11): 1677-1685, 2018 11.
Article in En | MEDLINE | ID: mdl-30311382
ABSTRACT
The use of genome-scale sequencing allows for identification of genetic findings beyond the original indication for testing (secondary findings). The ClinGen Actionability Working Group's (AWG) protocol for evidence synthesis and semi-quantitative metric scoring evaluates four domains of clinical actionability for potential secondary

findings:

severity and likelihood of the outcome, and effectiveness and nature of the intervention. As of February 2018, the AWG has scored 127 genes associated with 78 disorders (up-to-date topics/scores are available at www.clinicalgenome.org). Scores across these disorders were assessed to compare genes/disorders recommended for return as secondary findings by the American College of Medical Genetics and Genomics (ACMG) with those not currently recommended. Disorders recommended by the ACMG scored higher on outcome-related domains (severity and likelihood), but not on intervention-related domains (effectiveness and nature of the intervention). Current practices indicate that return of secondary findings will expand beyond those currently recommended by the ACMG. The ClinGen AWG evidence reports and summary scores are not intended as classifications of actionability, rather they provide a resource to aid decision makers as they determine best practices regarding secondary findings. The ClinGen AWG is working with the ACMG Secondary Findings Committee to update future iterations of their secondary findings list.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Human Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Human Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2018 Document type: Article
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