Upon clicking the "Similar Cases" tab, users are presented with a comprehensive list of variants that Franklin's AI has defined as relevant to their analysis. These variants typically share the same gene, domain, amino acid, or even the same variant.

Each variant is represented in a tile that showcases its similarity to the user's variant, protein effect, zygosity, and community frequency. Additionally, any public classification of the variant is also displayed, which users can click on to review the classification in detail.

Users can filter the volume of variants they are witnessing by utilizing the various filtration options available. These filters allow users to narrow down the results based on scope, effect, and Franklin's ACMG classification.

Furthermore, the "Similar Cases" feature allows users to connect with professionals who have experience with similar variants. Users can utilize the "Contact Member" option to initiate a conversation with these professionals, thus expanding their knowledge and understanding of the variant and gene.

Overall, the "Similar Cases" feature provides valuable insights and resources to users in their variant analysis, enabling them to make informed decisions and better understand the potential impact of the variant.