Interpret genetic test results with evidence-based clinical context. Pharmacogenomic implications, variant significance, and actionable clinical notes for each finding.
Copy variant names directly from the lab report for best accuracy.
Context helps prioritize which pharmacogenomic implications are most clinically relevant.
Cross-references reported variants against ClinVar, PharmGKB, and CPIC guidelines to provide classification context and known clinical associations.
Highlights gene-drug interactions and metabolizer status relevant to medication selection, dosing considerations, and adverse reaction risk.
Translates complex genomic findings into structured summaries suitable for clinical documentation and informed patient communication.
Assigns evidence-level indicators to each finding based on current literature strength — helping clinicians distinguish actionable from preliminary findings.
No. The tool provides contextual educational information from established genomic databases. Clinical interpretation and diagnostic decisions remain the responsibility of the ordering provider or genetic counselor.
The AI references ClinVar, PharmGKB, CPIC guidelines, and established pharmacogenomic literature. For the most current data, verify against the latest database versions.
The tool accepts structured variant reports — copy gene names and results directly from your lab report. Raw sequencing files (FASTQ, BAM, VCF) should be processed through appropriate bioinformatics pipelines first.
Genetic results should be communicated to patients by a trained clinician or genetic counselor who can provide appropriate context, answer questions, and address potential psychological impact.
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