You're taking advice meant for someone else's body.
Our at-home DNA test and pharmacogenomic report explain how your body actually processes food, medication, and sleep.
You eat well and buy the good brands. None of it knows whether your body actually uses that vitamin D, clears caffeine by lunch, or needs more sleep than the person beside you. One cheek swab reads the parts of your DNA that settle all of it, then hands you answers you can use this week.
One time
$249
$329
Your kit arrives in a few days. Swab, mail it back, and results land in the Biome app about two weeks later. You keep a copy of your DNA data for good.
Your results, in plain words
Your DNA stays yours.
Your DNA isn't ordinary data. It's permanent, it identifies you, and it says something about your family too. So we don't ask you to trust a promise, we chose structure. Our lab partner is a Delaware Public Benefit Corporation, legally bound to keep identifiable genetic data under your control and off the market. It does not, cannot, and will not sell your data.
Processed by CLIA- and CAP-accredited laboratories in the United States.
A Public Benefit Corporation
Our lab partner's purpose is written into its legal charter, not a marketing page. Its directors are bound to weigh your privacy, not only shareholder return, even when selling data would be the more profitable move.
Never for sale
Your individual genetic data is never sold or licensed. Not to researchers, pharmaceutical companies, insurers, or data brokers, and shared with law enforcement only under valid legal process.
Never used to train AI
Identifiable genomic data is never used to train AI models, and de-identified or aggregated genomic datasets are never sold or commercially distributed.
Yours to delete
There's no hidden research program behind your purchase. Your data is delivered to you, access is revocable, and a deletion request removes it rather than archiving it for later.
No gene names to google.
Most DNA reports read like a lab printout. Rows of letters, numbers, and Latin, and no idea what to do with any of it. Yours reads like a person talking. Each finding says what it means and the one change worth making.
Here's a sample of what lands in your app.
Get your results for $249Caffeine
Slow to clear it
Coffee lingers. Keep it before noon.
Vitamin D
You likely run low
Your body makes less from sunlight.
Omega-3
Weak converter
Get it from fish, not flax or seeds.
Training
Built for endurance
You answer better to longer efforts.
Sleep
Night-owl leaning
Your internal clock runs late.
Same coffee. Same dose. A completely different body.
Two people drink the same cup. One is wired until 2am, the other feels nothing. A lot of that gap is written in your genes, right next to the code that decides which vitamins help you and when your body wants to sleep. Most people never get to read it.
Read yours for $249Answers you can use tomorrow.
Six areas of your everyday life, read from the spots in your DNA that shape them.
Food and drink
Whether coffee keeps you up past midnight, how hard alcohol hits, why dairy turns on you, and why cilantro, asparagus, orange, or pineapple smells and tastes different to different people.
Supplements and vitamins
The ones your body uses well, and the ones it barely touches. Vitamin D, B12, folate, omega-3, plus context for how sun, season, supplements, and labs can change the picture.
Sleep
Early bird or night owl, written into your DNA before you ever set an alarm. Plus sleep-duration and sleep-stage context when the covered markers support it.
Training and recovery
Some bodies are built for the sprint, others for the long haul. Find out which one is yours, and how long you really need between hard days.
Medications
How your body tends to handle whole families of common medicine, from antidepressants and pain meds to statin and GLP-1 response context. The kind of thing worth bringing to your doctor, not the group chat.
Traits and resilience
Taste and smell quirks, body traits, and the stress and recovery tendencies you were born with and never picked.
Ancestry reference context
How your DNA compares with public reference groups, shown as broad genetic similarity with a confidence note, not ethnicity or identity.
Dozens of insights this test can surface.
Your DNA test reads hundreds of thousands of key spots in your DNA. Here is everything it can surface when those spots are covered. A few areas, medications especially, read more completely from a whole genome.
A DNA test reads a fixed set of spots, so a few of these (mostly polygenic scores) show up only if your sample covers them, and medications read more completely from a whole genome. Everything else is included.
Food & drink
Alcohol flush response
How quickly you clear acetaldehyde, the cause of alcohol flushing.
ALDH2 rs671
Alcohol metabolism
How fast your body breaks alcohol down.
ADH1B rs1229984
Lactose digestion
Whether you keep making lactase into adulthood for digesting dairy.
MCM6/LCT rs4988235
Caffeine metabolism
Whether you tend to clear caffeine quickly or slowly.
CYP1A2 rs762551
Caffeine intake tendency
Genetics linked to how much caffeine people gravitate toward.
AHR rs4410790
Caffeine sensitivity
How caffeine tends to affect your sleep and jitters.
ADORA2A rs5751876
Taste & smell
Bitter taste sensitivity
How strongly you taste bitter compounds (PTC/PROP).
TAS2R38 haplotype (rs713598, rs1726866, rs10246939)
Cilantro perception
Whether cilantro is more likely to taste soapy to you.
OR6A2 rs72921001
Asparagus odor detection
Whether you can smell the odor in urine after asparagus.
rs4481887
Orange smell identification
Genetic context for orange-smell recognition differences.
rs116058752 near ADCY2
If coveredPineapple smell identification
Genetic context for pineapple-smell recognition differences.
rs669453, rs61902559, OR11H7-region variants
If coveredSweet preference
Tendency toward sweet taste and preference.
Sweet-taste PRS/GWAS when present
If covered
Body traits
Earwax & body odor type
Wet vs dry earwax and underarm odor precursor production.
ABCC11 rs17822931
Freckling
Tendency to freckle and pigmentation response to sun.
IRF4 rs12203592
Eye color & pigmentation
Pigmentation context, including eye color.
HERC2/OCA2 rs12913832
Photic sneeze reflex
Tendency to sneeze when moving into bright light.
rs10427255, rs11856995
Ancestry reference context
Broad reference cluster
Which broad public reference cluster your DNA projects closest to, such as European, East Asian, African, South Asian, or Admixed American.
1000 Genomes PCA marker panel
If coveredNearby reference groups
Nearby 1000 Genomes population-label groups, shown as reference similarity rather than ethnicity, nationality, or identity.
1000 Genomes PCA marker panel
If coveredMarker overlap confidence
How many ancestry-panel markers were usable, so low-overlap results can be softened or hidden.
Panel overlap QC
If covered
Vitamins & nutrients
Vitamin D status
Tendency toward lower circulating vitamin D and how you transport it.
GC rs4588, GC rs2282679, CYP2R1 rs10741657, DHCR7/NADSYN1 rs12785878
Vitamin D sun-response context
How vitamin D genetics may interact with sun exposure, season, supplements, and lab values.
GC rs115366859; PDE3B, PSMA1, COPB1, CALCB, BMAL1/ARNTL loci
If coveredVitamin A conversion
How well you convert beta-carotene into active vitamin A.
BCO1 rs7501331
Folate pathway
Folate processing and homocysteine context.
MTHFR rs1801133, MTHFR rs1801131
Vitamin B12
B12 transport and status context.
TCN2 rs1801198, FUT2 rs602662
Vitamin C transport
Vitamin C transport tendency.
SLC23A1 rs33972313
If coveredOmega-3 conversion
How well you convert plant ALA into EPA and DHA.
FADS1 rs174537, rs174546, rs174547; FADS2 rs174575
Medication response
CYP2C19 substrates
Processing context for some antidepressants, reflux meds, and antiplatelet drugs.
CYP2C19 diplotype/phenotype
Stronger with whole genomeCYP2C9 substrates
Processing context for NSAIDs, warfarin, and phenytoin.
CYP2C9 diplotype/phenotype
Stronger with whole genomeWarfarin sensitivity
Warfarin sensitivity context.
VKORC1 genotype
Stronger with whole genomeStatin muscle symptoms
Context for statin-related muscle symptoms.
SLCO1B1 diplotype/phenotype
Stronger with whole genomeStatin and urate-drug transport
Additional transporter context for some statins and related medications.
ABCG2 diplotype/phenotype
Stronger with whole genomeGLP-1 medication response context
Inherited context for GLP-1 weight-loss response or nausea signals, for clinician review only.
GLP1R rs10305420, GIPR rs1800437
If coveredCYP2B6 substrates
Efavirenz and other drug metabolism context.
CYP2B6 diplotype/phenotype
Stronger with whole genomeCYP3A5 substrates
Tacrolimus and other CYP3A5 substrate context.
CYP3A5 diplotype/phenotype
Stronger with whole genomeDPYD substrates
Fluoropyrimidine tolerance context.
DPYD phenotype
Stronger with whole genomeThiopurine metabolism (TPMT)
Thiopurine metabolism context.
TPMT diplotype/phenotype
Stronger with whole genomeThiopurine sensitivity (NUDT15)
Thiopurine sensitivity context.
NUDT15 diplotype/phenotype
Stronger with whole genomeUGT1A1 substrates
Irinotecan and bilirubin metabolism context.
UGT1A1 diplotype/phenotype
Stronger with whole genomeG6PD context
Oxidative-hemolysis context for certain medications.
G6PD phenotype
Stronger with whole genomeCACNA1S substrates
Anesthesia-related malignant hyperthermia susceptibility context for volatile anesthetics and succinylcholine.
CACNA1S diplotype/phenotype
Stronger with whole genomeRYR1 substrates
Anesthesia-related malignant hyperthermia susceptibility context for volatile anesthetics and succinylcholine.
RYR1 diplotype/phenotype
Stronger with whole genomeCFTR substrates
Ivacaftor responsiveness context for people with cystic fibrosis.
CFTR diplotype/phenotype
Stronger with whole genomeCYP3A4 substrates
Quetiapine and other CYP3A4 substrate metabolism context.
CYP3A4 diplotype/phenotype
Stronger with whole genome
Sleep & chronotype
Morning vs evening tendency
Whether you lean toward being a morning or evening person.
Chronotype/morningness PRS
If coveredREM vs NREM sleep architecture
Genetic context for sleep-stage balance from device-measured sleep research.
MEIS1 rs113851554, rs4544423, rs182588061; KCNK9 rs888346
If coveredInsomnia tendency
Genetic context for insomnia tendency.
Insomnia PRS
If coveredSleep duration tendency
Genetic context for typical sleep duration.
Sleep-duration PRS
If covered
Fitness & performance
Power vs endurance
Muscle-fiber tendency toward sprint/power or endurance.
ACTN3 rs1815739
Endurance context
Additional endurance and power context.
ACE rs4343
Aerobic trainability
Mitochondrial and aerobic-response context.
PPARGC1A rs8192678
Endurance tendency
Polygenic endurance tendency.
Endurance PRS when present
If coveredAerobic capacity (VO2max)
Polygenic aerobic-capacity tendency.
VO2max PRS when present
If covered
Hormone pathways
Sex-hormone transport
Sex-hormone binding globulin context.
SHBG rs6259
Estrogen pathway
Aromatase and estrogen-pathway context.
CYP19A1 rs10046
Stress, longevity & antioxidants
Longevity-associated marker
A well-studied longevity-associated marker, for context.
FOXO3 rs2802292
Oxidative-stress pathway
Antioxidant enzyme and oxidative-stress context.
SOD2 rs4880
Stress-response pathway
Stress-response and cortisol-signaling pathway context.
FKBP5 rs1360780
Skin & connective tissue
Collagen & connective tissue
Collagen, tendon, and connective-tissue context.
COL1A1 rs1800012, COL5A1 rs12722
Skin matrix remodeling
Matrix remodeling and collagen context for skin.
MMP1 rs1799750
Skin oil-gland biology
Cosmetic skin-context signals tied to pilosebaceous-unit biology, not a dermatology diagnosis.
RXRA, SOX9, WNT and p53 pathway loci/PRS when present
If coveredGrowth & repair axis
IGF-1 and growth-hormone-axis context.
IGF1 rs35767, GHR rs6184
Inflammatory signaling
Baseline inflammatory-signaling context.
IL6 rs1800795, TNF/LTA rs1800629
Cognition & methylation
Dopamine & catecholamines
Dopamine, stress, and estrogen-pathway processing (COMT activity).
COMT rs4680
Neuroplasticity
BDNF-pathway context for learning and plasticity.
BDNF rs6265
One-carbon / methylation
Folate and methionine-cycle methylation context.
MTHFR rs1801133, rs1801131; MTR rs1805087; MTRR rs1801394
Where your DNA sits next to public reference groups.
Your report can compare your DNA with public reference-panel samples and show broad genetic similarity when enough markers are available. It is not an ethnicity test, a nationality label, or a family-origin verdict.
Broad cluster
European, East Asian, African, South Asian, or Admixed American reference-panel similarity.
Nearby labels
Reference groups like Puerto Rican, Iberian, Toscani, British, Yoruba, Bengali, or Han Chinese when the signal supports it.
Confidence
A marker-overlap quality note so limited samples are labeled carefully or not shown.
Example wording: “Your DNA projects closest to the European reference cluster, with nearby reference-panel groups including Iberian and Toscani. This is genetic similarity to public reference samples, not an ethnicity or country-of-origin result.”
Hundreds of thousands of the spots that actually matter.
Your DNA runs about three billion letters long. Most of them are identical from one person to the next. The interesting part is the small set of spots where we differ, and that's exactly where this test reads, across the well-studied markers tied to nutrition, vitamin D response, sleep, smell and taste, fitness, recovery, and how your body meets common medicine.
It's built for wellness you can act on, not for scaring you. We don't do disease reports. Anything that belongs in front of a doctor, we say so plainly.
Stop guessing what your body needs. Start reading it.
One swab today. Plain answers in about two weeks. The effort you already put into eating well, training, and sleeping finally points the right direction.
From swab to answers in about two weeks.
Swab your cheek
The kit shows up in a few days. Thirty seconds with a swab, no needles, no clinic, no fasting.
Mail it back
Drop the prepaid kit in the post. Track it the whole way, from your mailbox to our lab.
Read your answers
About two weeks later, your results open in the Biome app, written in plain language and ready to act on.
What it can tell you
✓Everyday tendencies for caffeine, alcohol, dairy, vitamins, omega-3, sleep, smell, taste, and training, read straight from the key spots in your DNA.
✓How your body tends to handle common medications, which is useful context to bring to a doctor before any decision.
✓Taste, smell, body traits, skin context, recovery, and the resilience tendencies you inherited.
✓Broad ancestry reference context when enough ancestry-panel markers are covered, framed as genetic similarity rather than ethnicity.
What it won't
It reads hundreds of thousands of well-studied spots, not every single letter of your DNA.
It doesn't diagnose disease or stand in for a clinical genetic test.
It can't promise how a drug will work, how long you'll live, or what your vitamin and hormone levels are right now.
Find out what your body actually needs.
One cheek swab. About two weeks. Answers you keep for good, written so you can act on them the same day they land.
Want every letter?
The full genome reads all of your DNA. Once, for the rest of your life.
Same plain answers, broader coverage, and one file that keeps turning up new insights as the science grows. You never have to swab again.
These results describe inherited tendencies and medication-response context from the markers we read. They're educational. They are not a diagnosis, a treatment plan, dosing instructions, or a substitute for clinician review. Some results may be worth discussing with your doctor.