BEGIN:VCALENDAR
VERSION:2.0
CALSCALE:GREGORIAN
METHOD:PUBLISH
PRODID://CGC//522003
BEGIN:VEVENT
DTSTAMP:20260612T182746
VTIMEZONE:America/New_York
DTSTART:20260623T160000Z
DTEND:20260623T170000Z
UID:522003
SUMMARY:ACMG Secondary Findings: Recommendation Overview and Discussion of Challenges in Practice
LOCATION:This is a live virtual event
DESCRIPTION:ACMG Secondary Findings: Recommendation Overview and Discussion of Challenges in Practice\n\n06/23/26 12:00 PM EST\n - 06/23/26 01:00 PM EST\Description:\nThe introduction of Secondary Finding (SF) genes by the American College of Medical Genetics and Genomics (ACMG) has standardized the process of reporting variants and follow up counseling. While most of the SF genes are associated with autosomal dominant genetic conditions, laboratories may find variants in the SF genes associated with recessive conditions that may need further evaluation. \n\nJoin Dr. Mahmoud Aarabi for an insightful and practical review of ACMG Secondary Finding genes, including emerging considerations for recessive genetic conditions and CNV reporting following microarray and sequencing-based testing. This talk will review the SF genes and provide some practical considerations and clinical examples applicable to recessive genetic conditions and CNVs. \n\nLevel of Instruction: Intermediate\n\nLearning Objectives: At the end of this webinar, participants will be able to:\n\n\n	Apply ACMG guidelines to the interpretation and reporting of variants identified in secondary finding (SF) genes.\n	Discuss secondary finding (SF) genes associated with recessive genetic conditions and their unique reporting strategy.\n	Identify copy number variants in secondary finding (SF) genes and their reporting considerations.\n\n\Location:\nThis is a live virtual event\n\n,
X-ALT-DESC;FMTTYPE=text/html:ACMG Secondary Findings: Recommendation Overview and Discussion of Challenges in Practice<br /><br />06/23/26 12:00 PM EST - 06/23/26 01:00 PM EST<br />Description:<br /><p style="text-align: justify;"><span style="font-size:16px"><span style="font-family:arial,helvetica,sans-serif">The introduction of Secondary Finding (SF) genes by the American College of Medical Genetics and Genomics (ACMG) has standardized the process of reporting variants and follow up counseling. While most of the SF genes are associated with autosomal dominant genetic conditions, laboratories may find variants in the SF genes associated with recessive conditions that may need further evaluation.&nbsp;<br />
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Join Dr. Mahmoud Aarabi for an insightful and practical review of ACMG Secondary Finding&nbsp;genes, including emerging considerations for recessive genetic conditions and CNV reporting following microarray and sequencing-based testing. This talk will review the SF genes and provide some practical considerations and clinical examples applicable to recessive genetic conditions and CNVs.&nbsp;</span></span><br />
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<span style="font-size:16px"><span style="font-family:arial,helvetica,sans-serif"><span style="color:#008080"><strong>Level of Instruction: </strong></span>Intermediate</span></span><br />
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<span style="font-size:16px"><span style="font-family:arial,helvetica,sans-serif"><span style="color:#008080"><strong>Learning Objectives:</strong></span> At the end of this webinar, participants will be able to:</span></span></p>

<ol>
	<li><span style="font-size:16px"><span style="font-family:arial,helvetica,sans-serif">Apply ACMG guidelines to the interpretation and reporting of variants identified in secondary finding (SF) genes.</span></span></li>
	<li><span style="font-size:16px"><span style="font-family:arial,helvetica,sans-serif">Discuss secondary finding (SF) genes associated with recessive genetic conditions and their unique reporting strategy.</span></span></li>
	<li><span style="font-size:16px"><span style="font-family:arial,helvetica,sans-serif">Identify copy number variants in secondary finding (SF) genes and their reporting considerations.</span></span></li>
</ol>
<br />Location:<br />This is a live virtual event<br /><br />,  
PRIORITY:3
TRANSP:TRANSPARENT
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DESCRIPTION:Reminder
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