Live Demo — No download needed

See VariantTriage
in action

Load one of our demo datasets or upload your own VCF file. Full analysis, right in your browser.

👁️
Retinitis Pigmentosa
12 variants · RPGR, USH2A, RHO, RPE65
🎗️
Hereditary Cancer
12 variants · BRCA1, BRCA2, TP53, MSH2
🫀
Cardiology Panel
10 variants · MYBPC3, SCN5A, LMNA

Demo data only — no account or download required

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Total variants
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Pathogenic
—
Likely Path.
—
VUS
—
Benign
Variants 0
Chr Position Gene Ref → Alt Type Severity
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Gene Information
👆

Click any row to see
detailed gene information

Severity Distribution
Pathogenic
0
Likely Path.
0
VUS
0
Benign
0
Unknown
0

Analyze your own VCF files

This demo shows 12 curated variants. Upload your own VCF file to get full AI-powered analysis — free to start, no download needed.

  • Upload unlimited VCF files
  • AI Clinical Summary per variant
  • ClinVar live lookup
  • PDF clinical report generator
  • CSV / Excel / TSV export
Create free account → Or try the browser app without an account →