Exome/genome sequencing has the ability to identify medically actionable incidental, or secondary, findings that are unrelated to the indication for testing. These results are optional for individuals/families to receive and there are several important points to consider when consenting for genomic testing. This webinar will review basic information about secondary findings, including recent updates to the ACMG recommended gene list, explore various psychosocial considerations related to secondary findings, and review case examples of real life implications of identification of secondary findings, with an emphasis on potential complexities important for genetic counselors to consider.
Level of Instruction: Intermediate
Only the live session qualifies for CEUs but when possible, we host the recordings on our website and NSGC recommends participants to use their personal email instead of work email addresses to ensure they receive their CEU certificates.
Ambry Genetics is approved as a provider for continuing education program by NSGC and ASCLS P.A.C.E ® Program.