// GENOMICS ENGINE

Your code. Decoded.

Upload your 23andMe, AncestryDNA, or VCF file. Get pharmacogenomic guidance for 14+ common medications, disease risk scoring (APOE, BRCA, MTHFR), and phenotypic trait analysis — all backed by CPIC, PharmGKB, and NIH ClinVar.

// THREE ENGINES

One upload, three analyses.

Every file run through Hunuu's genomics service produces three distinct reports, each tied to the peer-reviewed clinical guideline that backs it.

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Pharmacogenomics

How your body processes codeine, warfarin, SSRIs, clopidogrel, and 10+ other common drugs. Backed by CPIC guidelines.

🛡️

Disease Risk

APOE (Alzheimer's), BRCA1/2 (cancer), MTHFR (folate), Factor V (clotting), and 23 more actionable variants. Backed by ClinVar.

🧬

Traits & Ancestry

Caffeine metabolism, lactose tolerance, alcohol sensitivity, muscle-fiber composition, sleep chronotype, and more.

SAMPLE REPORT

Variant highlights

CYP2D6 *1/*4

Intermediate metabolizer — reduce codeine dose ~25%

WATCH

APOE ε3/ε3

Average Alzheimer's risk — standard prevention applies

CLEAR

MTHFR C677T het

Mildly reduced folate metabolism — consider methylfolate

WATCH

BRCA1/BRCA2

No pathogenic variants detected

CLEAR

VKORC1 -1639G>A

Warfarin sensitive — start at 30% lower dose

ACTION

🔒

Raw files are never stored. Your uploaded 23andMe or VCF file is parsed in memory during processing and immediately discarded. Only the inference output — the variant analysis and recommendations — is saved to your account. GINA-compliant. No insurer, no employer, no data broker gets your genome.

// THE FLOW

Three steps, three minutes.

📱

01. Upload in App

Open Hunuu iOS/Android → Genomics tab → pick your 23andMe, AncestryDNA, or VCF file. Parsing happens on secure servers.

⚙️

02. AI Analysis

Our TensorFlow-backed variant engine cross-references your SNPs against CPIC + ClinVar. ~90 seconds.

🖥️

03. Web Upload

Upload and view results directly from the desktop site — for users without a phone.

// UNLOCK YOUR CODE

Decode yourself.

Genomics is included with Founders Club ($25 lifetime) and all paid tiers. Full pharmacogenomic analysis, lifetime of updates as new variants are added.

JOIN FOUNDERS CLUB — $25 Compare Tiers