ACMG Highlights

Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Hearing-Loss-Practice-Resource

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Carnitine Uptake Defect (CUD; Primary Carnitine Deficiency) Newborn Screening Algorithm
Carnitine Uptake Defect (CUD; Primary Carnitine Deficiency) Newborn Screening Algorithm

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Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency Newborn Screening Algorithm
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency Newborn Screening Algorithm

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Upcoming Events

New ACCME standards are now in effect as of January 1, 2022
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Medical Necessity Webinar Series from the National Coordinating Center for the Regional Genetics Networks (NCC) and the Catalyst Center

Friday, May 20, 2022
Time:1:00 pm- 2:00 PM ET

Interested in learning more about what medical necessity is and how evidence is used to inform policy? Join the National Coordinating Center for the Regional Genetics Networks (NCC) and The Catalyst Center for Part 2 of a three-part webinar series about medical necessity.
Register Here!

ClinGen Somatic Cancer and VICC Virtual Molecular Tumor Board Case Series
Tuesday, May 24, 2022
Time: 11:00 am - 12:00 pm ET

All medical and healthcare professionals and researchers interested in understanding cancer genomic testing and somatic and germline variant interpretation methods. This series is presented as a collaboration between ClinGen Somatic, VICC, and ACMG consortia.
Register Here!


ACMG Genetics101 for Healthcare Providers
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2022 ACMG Annual Clinical Genetics Meeting Digital Edition
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News and Releases

The American College of Medical Genetics and Genomics Publishes Clinical Practice Resource on Hearing Loss
ACMG-Publishes-Clinical-Practice-Resource-on-Hearing-Loss.T.5.4__BE final

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New “Genetics101 for Healthcare Providers” Online Course Addresses Gap in Education for Nongenetics Healthcare Providers: Course will be Featured in the American Medical Association’s AMA Ed Hub™
Genetics101_T_3.21.RS

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Kushani Jayasinghe, MBBS Receives the 2022 Richard King Award for Best Publication by a Trainee in Genetics in Medicine
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