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EboMedAI Subscription
EboMedAI Subscription
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Product Description:
EboMedAI Consultant is your personal AI-powered genetic consultant, designed by geneticists, medical doctors, bio-information experts, and AI scientists. It helps you interpret your genetic test results and understand potential health risks, variant significance, and lifestyle implications based on your DNA. Data Security Notice:To fully protect your privacy and comply with global genetic data safety standards, your uploaded report and genetic data are NOT stored on our servers. Therefore, please keep the session window open while interacting with the AI. If the page is closed or refreshed, you will need to re-upload your genetic report.
Key Features
· AI-powered analysis of your genetic report (e.g., EboGenes Genetic Report, Blueprint Report, AncestryDNA, whole exome, or genome)
· Purpose-Built for Genetics: Unlike generic AI like ChatGPT, EboMedAI is trained and fine-tuned by clinical geneticists, AI scientists, and physicians specifically for interpreting genetic data.
· Structured Variant Analysis: Automatically identifies and prioritizes clinically relevant mutations using 170+ global variant databases (ClinVar, gnomAD, HGMD, etc.).
· Personalized Health Risk Insights: Generates risk assessments based on genotype–phenotype relationships, with disease association scoring—not just generic text responses.
· Scientific Evidence Linking: Every interpretation includes references from over 35 million scientific and clinical publications—traceable and credible.
· Human-Centered Explanations: Translates complex variant data into plain language, helping users understand without a medical background.
· Report-Aware Conversations: Unlike ChatGPT, EboMedAI “remembers” your uploaded report structure throughout the session, allowing focused and context-aware answers.
· Privacy by Design: Your genetic data is never stored on our servers. All analysis runs in-session only. No uploads are saved, ensuring full data privacy compliance.
· Tailored Outputs: Offers downloadable, doctor-friendly summaries and variant-level insights that are not available through general AI tools.
