Upload your 23andMe raw data. Get a comprehensive AI health report with disease risk analysis, drug interactions, and an actionable protocol.
No subscription. No recurring charges. Your report forever.
Download your raw data from 23andMe and send us the genome.txt file.
Our pipeline cross-references your SNPs against ClinVar and PharmGKB databases.
Get three detailed reports: health optimization, disease risk, and an actionable protocol.
200+ curated SNPs: methylation (MTHFR, COMT), detox (CYP450), inflammation (IL-6, TNF), cardiovascular risk, and nutrient metabolism.
Your genome checked against 341,000 ClinVar variants. Pathogenic and drug response variants highlighted with clinical significance stars.
PharmGKB pharmacogenomic data shows how your genetics affect drug metabolism. Know which medications work better for your genotype.
Personalized supplement and lifestyle protocol based on YOUR genetic variants. Not generic advice.
67 trait SNPs: eye color prediction, hair texture, skin type, taste sensitivity, morphological features, vision.
Your genome data is processed in an isolated environment and deleted after report generation. We never store or share your genetic data.
⭐⭐⭐ [HETERO] MTHFR NP_005948.3:p.Ala222Val (rs1801133 CT) Drug response — Methotrexate sensitivity; Neural tube defects risk Action: Consider methylfolate supplementation ⭐⭐⭐ [HETERO] CYP2D6 (rs3892097 GA) Poor metabolizer phenotype — affects codeine, tamoxifen, SSRIs Action: Discuss with physician before prescribing these drug classes ⭐⭐ [HOMO] COMT Val158Met (rs4680 AA) Worrier genotype — slower catecholamine clearance Action: Magnesium, L-theanine, methylation support ⭐⭐ [HETERO] IL6 (rs1800795 CG) Elevated inflammatory baseline Action: Anti-inflammatory protocol (omega-3, curcumin) --- COMPREHENSIVE SNP ANALYSIS --- Category: Methylation & Detox MTHFR C677T: CT — Heterozygous carrier. ~35% reduced function. COMT Val158Met: AA — Slow COMT. Low dopamine clearance. VDR Taq: AG — Moderate vitamin D receptor activity.
Actual report is 15-30 pages with full clinical context and personalized recommendations.
Your 23andMe raw data file (genome.txt). Download from 23andMe Settings → 23andMe Data → Download Raw Data. AncestryDNA files also work.
Yes. Your genome file is processed locally and deleted after report generation. We never store, share, or sell genetic data.
23andMe covers ~10 conditions. We analyze 200+ health SNPs, 341K ClinVar variants, PharmGKB drug interactions, and generate a personalized action protocol. Much deeper.
No. This is for educational purposes. Discuss findings with your healthcare provider.
Analysis takes ~5 minutes. Report delivered via email within 24 hours.
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The same databases trusted by researchers and clinicians worldwide.