Join us in empowering those impacted by a 16p11.2 variant as we focus on raising awareness, creating connections, and advancing research.16p11.2 Genetic Foundation works to treat and integrate 16p11.2 genetic variances seamlessly throughout the health, education and societal landscapes by 2030. We do it for our children.16p11.2 variants are caused by a mutation that deletes or duplicates a portion of the 16th chromosome. These variations can cause delays in speech and language development, developmental delays and learning difficulties, increases susceptibility to autism spectrum disorder, low muscle tone causing physical delays and obesity, seizure disorders, and other developmental issues. The syndrome's presentation varies between each individual making diagnosis and universal treatment difficult.Your support helps us families affected by a 16p11.2 variant find hope and connection. Thank you for walking with us on this journey.