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<title>Ambry Genetics News by Category: Variant of Unknown Significance</title>
<link>https://blog.ambrygen.com/list/category/Variant%20of%20Unknown%20Significance</link>
<description>Find the latest Ambry Genetics news by category: Variant of Unknown Significance</description>
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<title>Ambry Genetics Blog</title>
<link>https://blog.ambrygen.com/list/category/Variant%20of%20Unknown%20Significance</link>
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<title>Striking the Perfect Balance in Designing Hereditary Cancer Tests: The Ambry Approach</title>
<link>https://blog.ambrygen.com/ambry/post/363/striking-the-perfect-balance-in-designing-hereditary-cancer-tests-the-ambry-approach</link>
<description>Ambry's balanced approach to designing hereditary cancer tests ensures our panels remain relevant and impactful, helping clinicians manage hereditary cancer risk with confidence.</description>
<pubDate>Thu, 31 Oct 24 08:40:00 -0700</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<title>The Evolution of Hereditary Cancer Testing: Why Pan-Cancer Panels Are the Future of Genetic Risk Assessment</title>
<link>https://blog.ambrygen.com/ambry/post/362/the-evolution-of-hereditary-cancer-testing-why-pan-cancer-panels-are-the-future-of-genetic-risk-assessment</link>
<description>Pan-cancer panels offer more comprehensive diagnoses, personalized risk assessments, and targeted prevention and treatment strategies.</description>
<pubDate>Thu, 17 Oct 24 08:18:00 -0700</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>APC: New Takes on an Old Gene</title>
<link>https://blog.ambrygen.com/ambry/post/344/apc-new-takes-on-an-old-gene</link>
<description>Pathogenic variants in the APC gene cause conditions such as FAP and GAPPS. Marcy Richardson breaks down genotype-phenotype correlations and how they cause one condition or presentation versus another.</description>
<pubDate>Thu, 28 Mar 24 03:45:00 -0700</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>Greater than the Sum of its Parts: Gene-Disease Validity and Breast Cancer</title>
<link>https://blog.ambrygen.com/ambry/post/338/greater-than-the-sum-of-its-parts-gene-disease-validity-and-breast-cancer</link>
<description>Jennifer Herrera-Mullar discusses the correlation between breast-cancer associated genes and gene-disease validity</description>
<pubDate>Tue, 05 Mar 24 03:00:00 -0800</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>Variant Interpretation in Real Time: Sometimes it Takes a Village</title>
<link>https://blog.ambrygen.com/ambry/post/337/variant-interpretation-in-real-time-sometimes-it-takes-a-village</link>
<description>Genetic counselors explain how a CDH1 variant was classified as likely pathogenic from VUS status.</description>
<pubDate>Fri, 23 Feb 24 08:36:00 -0800</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<title>The Path to Clinical Relevance: What a Study on RAD51C Reveals about Resolving VUS</title>
<link>https://blog.ambrygen.com/ambry/post/328/the-path-to-clinical-relevance-what-a-study-on-rad51c-reveals-about-resolving-vus</link>
<description>Marcy Richardson, PhD discusses variant interpretation, VUS, and recategorizing missense genes with an example from Hu et al's recent publication on RAD51C.</description>
<pubDate>Tue, 19 Dec 23 08:22:00 -0800</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>Peace of Mind: Michelle Majewski Trusts the Patient for Life Program to Share Answers for Her Son Owen</title>
<link>https://blog.ambrygen.com/patient/post/324/peace-of-mind-michelle-majewski-trusts-the-patient-for-life-program-to-share-answers-for-her-son-owen</link>
<description>Michelle Majewski juggles a career as a sales account executive, husband, and son Owen, who has extra medical needs, without a clear diagnosis. The search for answers used to keep Michelle up at night, before ExomeNext.</description>
<pubDate>Tue, 14 Nov 23 06:27:00 -0800</pubDate>
<source>Ambry Genetics Patient Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>Genetics in Medicine publication demonstrates a 10% lower rate of VUS with WES/WGS compared to panels</title>
<link>https://blog.ambrygen.com/ambry/post/319/genetics-in-medicine-publication-demonstrates-a-10-lower-rate-of-vus-with-wes-wgs-compared-to-panels</link>
<description>A discussion of VUS and explanation of their significance, highlighting Ambry's collaboration in the GIM publication, The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change.</description>
<pubDate>Wed, 20 Sep 23 04:18:00 -0700</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
</item>
<item>
<title>5 Things You Need to Know about Ambry’s Variant Review Process</title>
<link>https://blog.ambrygen.com/ambry/post/265/5-things-you-need-to-know-about-ambry-s-variant-review-process</link>
<description>Genetic testing laboratories should have a defined process to regularly review the evidence for genetic variants, so they can eventually come to a verdict and provide a more clear answer.</description>
<pubDate>Thu, 23 Aug 18 12:45:00 -0700</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>Dr. Rachid Karam Discusses Variant Classification at 2017 ACMG Annual Meeting</title>
<link>https://blog.ambrygen.com/ambry/post/172/dr-rachid-karam-discusses-variant-classification-at-2017-acmg-annual-meeting</link>
<description>During the 2017 ACMG Annual Meeting, Rachid Karam, MD, PhD, discussed how understanding VUS results can help clinicians create medical management plans for their patients.</description>
<pubDate>Thu, 30 Mar 17 19:06:00 -0700</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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<item>
<title>RNA Labs—How they Impact the Medical World</title>
<link>https://blog.ambrygen.com/ambry/post/163/rna-labs-how-they-impact-the-medical-world</link>
<description>By having the ATG Lab at Ambry, it is possible to further refine VUS results and look beyond DNA in order to determine the benign or pathogenic status of splicing.</description>
<pubDate>Thu, 02 Mar 17 23:46:00 -0800</pubDate>
<source>Ambry Genetics Ambry Blog</source>
<category>Variant of Unknown Significance</category>
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