From coordinates to clinician-ready interpretation in three steps.
Enter genomic coordinates, assembly, and variant type. Optionally add HPO phenotype terms for richer matching.
Explore an aggregated evidence dashboard: overlapping genes, clinical significance, population frequencies, and literature.
Receive a structured AI interpretation with source-linked explanation, ACMG-aligned classification, and next steps.
Get API access, SSO, private deployment options, validation support, and institution-level workflows.
Gene-Cortex.com supports evidence aggregation and interpretation workflows. It does not replace professional clinical judgment. AI-generated outputs should be reviewed against the cited evidence before any clinical action.