Genomics · how it works
Your DNA,
read on your device.
Bring a raw file from 23andMe, AncestryDNA, or a whole-genome sequence. Further reads it locally, fills in the positions your chip never measured, and turns it into plain-English insight you can actually use. Not a single base ever leaves your machine.
30.4M variants·GRCh38·Read entirely on your Mac
From a raw chip to the whole genome.
The figures and results shown below are an illustrative example profile, not your own results.
612,431
positions genotyped
Read your raw chip
A 23andMe v5 export directly measures about 612,431 positions across your genome.
30.4M
variants resolved
Phase and impute
Statistical phasing against the 1000 Genomes + HGDP reference panel fills in the positions your chip skipped, at concordance R² > 0.8 for common variants.
8
readout areas
Read across the genome
Directional trait scores, drug-processing tendencies, carrier checks, and benign traits all read from the same file, computed and kept on your Mac.
What it reads
Everything your DNA points to, in plain English.
Pharmacogenomics
How your body tends to process compounds.
About one in four prescription drugs is broken down by a small set of genes. Reading yours describes a general tendency in how your body processes certain everyday compounds, useful background for a conversation with your clinician.
- Common prescription drugsTypical processing
- Statin responseTypical
- Warfarin (blood thinner)Increased tendency
- FluoropyrimidinesTypical
Mapped to CPIC pharmacogenomic guidance. Educational context for you and your clinician, not a prescription.
Directional loading
Which way your DNA leans.
A polygenic score adds up millions of tiny genetic effects into a single directional signal, which way your DNA leans for a trait. It's context for a conversation with your clinician, not a diagnosis, and it's less precise for non-European ancestries.
- Heart healthLeans higher
- Memory & agingLeans slightly higher
- Blood-sugar handlingLeans lower
- Heart rhythmAround average
Directional signals only, no percentiles or absolute risk. Less precise for non-European ancestries. Observations, not a diagnosis.
Nutrition & food response
How your body reacts to what you eat.
Small genetic differences change how you handle caffeine, dairy, alcohol, and fat. None of it is destiny, but it explains a lot of what you already feel.
- CaffeineSlower processing
- LactoseTolerant
- Saturated fatStronger LDL response
- Vitamin DLower baseline
Carrier status
What you could pass on.
A recessive condition needs two broken copies to show up. Carrying one usually means nothing for your own health, but it matters for family planning.
- Hereditary hemochromatosisCarrier · one copy
- Cystic fibrosisNot detected
- Hereditary breast & ovarianNot detected
- Tay-SachsNot detected
Traits
The small stuff that's just you.
Not medical, just human. Hundreds of little readouts, from eye color to whether cilantro tastes like soap.
- Eye colorLikely brown / hazel
- ChronotypeSlight morning preference
- CilantroTastes normal, not soapy
- Earwax typeWet (typical European)
Your DNA never leaves your device.
Genomes can never be revoked or changed. Further parses your raw file locally and reads only the positions needed for analysis. Your raw data is never uploaded, never logged, never shared. Same variant, same finding, every time.
See it run on your own DNA.
Observations to raise with your clinician. Informational only, not medical advice.