doi: https://doi.org/10.7303/syn49223352 event: Hack for NF 2022 summary: We constructed a causal inference model to explain how the variables in a given germline dataset are related to each other. We then gave additional inputs for individual variants that are specific to the NF1 gene that will supplement and modify existing pathogenicity scoring systems. Challenge: Challenge 2 initiative: 2022 Hack for NF studyStatus: Completed fundingAgency: CTF tab1wikipointer: syn49223352/wiki/620199 acknowledgementStatements: If you use data/concepts from this hackathon project in a publication or talk, please acknowledge the authors of this hackathon project. In addition, please acknowledge the Children's Tumor Foundation and NF Data Portal using the following statement: "The results published here are in whole or in part based on data/concepts made available through the NF Open Science Initiative and CTF Hack for NF 2022."