Whole Genome Sequencing provides answers where other tests cannot. In this case study, see how WGS plus RNA helped end the diagnostic odyssey for a patient with Sanfilippo Syndrome. hubs.ly/Q04zrxGq0

For Breast Cancer Awareness Month, Jewel Wasson, MS, CGC, joins the Gene Scene to discuss pathogenic variants in BRCA2, BRCA2-related cancer predisposition, and BRCA2-related Fanconi anemia. #GeneScene #GeneChat #GeneticTesting hubs.ly/Q04zhz-t0

Whole Genome Testing is now available from Ambry. Read the press release: hubs.ly/Q04zFhLR0

Learn more: hubs.ly/Q04zhzkg0

COMING SOON The Next Generation of Clinical Genome Testing Built for more answers, more access, and more support. October 2026

October 2026.

Coming soon.

Join us for a webinar on Wednesday, October 7. Elizabeth Jordan, MMSc, CGC, will explore the evolving landscape of cardiovascular genetics in diverse populations, with a focus on how diverse representation shapes discovery, interpretation, and clinical care. Register now: hubs.ly/Q04zmTcQ0

COMING SOON A More Equitable Clinical Genome

Brooke Sample, MS, CGC, explores pathogenic variants in the DES gene, which have been associated with a spectrum of DES­-related myopathies, including dilated cardiomyopathy (DCM) and arrhythmogenic right ventricular cardiomyopathy (ARVC), and myofibrillar myopathy (MFM). #GeneScene #GeneChat #DES #Cardio hubs.ly/Q04zh7Vt0

Thank you for joining Ambry in recognizing National Hereditary Cancer Week. You can use the hashtag #NHCW2026 to share your story. Visit the Ambry website to learn more about hereditary cancer testing options. For more resources, click here for a cultivated list from Marleah Dean Kruzel, PhD. hubs.ly/Q04z2Kj40 #Previvor #HereditaryCancer #GeneChat #DigitalHealth #BRCA #LynchSyndrome

As we recognize National Hereditary Cancer Week, we present these "Myth-busters" to debunk common misconceptions about hereditary cancer testing (HCT). #NHCW2026 #HereditaryCancer #GeneChat #GeneticTesting

Join Ambry at the American Academy of Pediatrics (AAP) Annual Meeting October 3-5 in San Diego. For families looking for answers, genetic testing and proactive reanalysis can help end the diagnostic odyssey. Visit our booth or meet with one of our representatives to explore how we are advancing clinical genomics for children with intellectual disability and global developmental delay. Learn more or request a meeting. hubs.ly/Q04yMkbY0 #AAP2026 #genetictesting #raredisease

It’s important to discuss health history with family members. But even when you get a relevant test result, life can get in the way. Marleah continues illuminating the path of her previvor journey. hubs.ly/Q04yXzhb0

Marleah Dean Kruzel, PhD, joined us to recognize National Previvor Day by sharing her personal "Journey to Previvorship." She uses her unique perspective as a BRCA2 previvor to empower others who carry a genetic predisposition to cancer. Watch the video and click to learn more. hubs.ly/Q04yJxFl0 hubs.ly/Q04yJxCz0 #NHCW2026 #Previvor #HereditaryCancer #GeneChat #breastcancer #Oncology #Healthcare #NarrativeMedicine #GeneticTesting #BRCA #LynchSyndrome

At Ambry, we are passionate about offering genetic testing that provides patients with information to inform their healthcare journey. Inherited gene mutations account for 5-10% of all cancers. Many individuals with an inherited mutation remain unaware of their risk and available medical options. How do you know if you should get genetic testing? This page explains how to talk to your healthcare provider and determine your risk. Learn more: hubs.ly/Q04yyRzT0

Join Kristina Garcia, MGCS, CGC, in the Gene Scene as she discusses pathogenic variants in this gene, which are known to cause SDHC-related hereditary pheochromocytoma-paraganglioma (PCC-PGL). hubs.ly/Q04yyQQw0 #GeneScene #GeneChat #GeneticTesting

In recognition of Hereditary Cancer Awareness Week, Ambry answers the question “What is hereditary cancer?”  hubs.ly/Q04yq4sb0

Shelly McQuaid, MS, CGC, explores HNF1A-related maturity-onset diabetes of the young (MODY), type 3, in this week's #GeneScene. #GeneChat #genetictesting hubs.ly/Q04y1Wks0

Ambry Genetics is a proud sponsor of the CNS annual meeting. Visit booth 401 to learn how our tests can help you and your patients find clearer answers sooner—because every day without a diagnosis matters. We look forward to seeing you in Montreal! #CNSAM #ChildNeurologySociety #PediatricNeurology