Simons Searchlight is an online community that supports families with rare genetic changes (also called “genomic variants”) associated with features of autism and developmental delay. They provide access to resources, information, and family support. Simons also provides an opportunity for families to participate in research. We encourage new families to follow this link to join Simons Searchlight and begin adding to the body of growing information of the symptoms associated with HNRNPH2 mutations. Also, see below for step-by-step instructions.