Most DNA kits read a sliver. This reads all of it.
A whole genome sequencing test that reads 100% of your DNA, not just the fraction of one percent covered by typical at-home DNA tests.
A basic kit checks a few pre-picked spots. This sequences every letter of your DNA, cover to cover, then turns it into plain answers about food, supplements, sleep, training, and the medicines you take. For far less than a private doctor's workup.
Founding price
$349
$429
Includes the at-home swab kit, prepaid return, order tracking, results in the Biome app, and a portable copy of your genome to keep. Most results are ready within two to three weeks after the lab receives your sample.
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.
We read all of it.
A basic DNA test skims a set of pre-picked spots. The full genome reads every letter, cover to cover. It's the difference between flipping through one page and reading the whole book, and it's why a missing marker almost never leaves you with a blank.
Read all of yours for $349
You've taken a DNA test. You've never actually had your DNA read.
The cheap kits check a fraction of one percent and call it done. Reading the whole thing is what your doctor would do if you handed them the keys. The people who go this deep tend to be the ones who want the full picture.
Read all of it for $349Plain answers, read from your whole genome.
Every finding arrives in plain language, with what it means and what to do next. No gene names to decode on your own.
Food, drink, and vitamins
Caffeine, alcohol, dairy, smell and taste quirks, and which vitamins your body actually puts to work. Vitamin D, B12, folate, omega-3, plus sun and season context.
Medications
How your body tends to meet whole families of medicine, from antidepressants and common painkillers to blood thinners, statins, and GLP-1 response context for clinician review.
Sleep and energy
Whether you're wired for early mornings or late nights, how caffeine quietly fits into either one, and sleep-stage context as research keeps improving.
Training and recovery
Power or endurance, how your body answers training, and how much rest it really needs to come back stronger.
Hormones and resilience
Inherited tendencies across hormone, stress, and inflammation pathways, framed as context rather than a verdict.
Longevity and aging
Markers tied to healthy aging, resilience, antioxidants, and cosmetic skin biology, read as genetic context, never as a countdown or diagnosis.
Ancestry reference context
Genome-wide similarity to public reference samples, with broad clusters, nearby reference labels, and a confidence note.
Dozens of insights this test can surface.
Your whole-genome test reads all of your DNA, so coverage gaps are rare. Here is everything it can surface, including the areas a basic DNA test can only read in part.
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
Pineapple smell identification
Genetic context for pineapple-smell recognition differences.
rs669453, rs61902559, OR11H7-region variants
Sweet preference
Tendency toward sweet taste and preference.
Sweet-taste PRS/GWAS when present
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
Nearby reference groups
Nearby 1000 Genomes population-label groups, shown as reference similarity rather than ethnicity, nationality, or identity.
1000 Genomes PCA marker panel
Marker overlap confidence
How many ancestry-panel markers were usable, so low-overlap results can be softened or hidden.
Panel overlap QC
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
Vitamin 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
Omega-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
CYP2D6 substrates
Processing context for many antidepressants, pain meds, and beta blockers. Reliable only from a whole genome (copy-number and hybrid alleles).
CYP2D6 diplotype/phenotype
CYP2C9 substrates
Processing context for NSAIDs, warfarin, and phenytoin.
CYP2C9 diplotype/phenotype
Warfarin sensitivity
Warfarin sensitivity context.
VKORC1 genotype
Statin muscle symptoms
Context for statin-related muscle symptoms.
SLCO1B1 diplotype/phenotype
Statin and urate-drug transport
Additional transporter context for some statins and related medications.
ABCG2 diplotype/phenotype
GLP-1 medication response context
Inherited context for GLP-1 weight-loss response or nausea signals, for clinician review only.
GLP1R rs10305420, GIPR rs1800437
CYP2B6 substrates
Efavirenz and other drug metabolism context.
CYP2B6 diplotype/phenotype
CYP3A5 substrates
Tacrolimus and other CYP3A5 substrate context.
CYP3A5 diplotype/phenotype
DPYD substrates
Fluoropyrimidine tolerance context.
DPYD phenotype
Thiopurine metabolism (TPMT)
Thiopurine metabolism context.
TPMT diplotype/phenotype
Thiopurine sensitivity (NUDT15)
Thiopurine sensitivity context.
NUDT15 diplotype/phenotype
UGT1A1 substrates
Irinotecan and bilirubin metabolism context.
UGT1A1 diplotype/phenotype
G6PD context
Oxidative-hemolysis context for certain medications.
G6PD phenotype
CACNA1S substrates
Anesthesia-related malignant hyperthermia susceptibility context for volatile anesthetics and succinylcholine.
CACNA1S diplotype/phenotype
RYR1 substrates
Anesthesia-related malignant hyperthermia susceptibility context for volatile anesthetics and succinylcholine.
RYR1 diplotype/phenotype
CFTR substrates
Ivacaftor responsiveness context for people with cystic fibrosis.
CFTR diplotype/phenotype
CYP3A4 substrates
Quetiapine and other CYP3A4 substrate metabolism context.
CYP3A4 diplotype/phenotype
Sleep & chronotype
Morning vs evening tendency
Whether you lean toward being a morning or evening person.
Chronotype/morningness PRS
REM vs NREM sleep architecture
Genetic context for sleep-stage balance from device-measured sleep research.
MEIS1 rs113851554, rs4544423, rs182588061; KCNK9 rs888346
Insomnia tendency
Genetic context for insomnia tendency.
Insomnia PRS
Sleep duration tendency
Genetic context for typical sleep duration.
Sleep-duration PRS
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
Aerobic capacity (VO2max)
Polygenic aerobic-capacity tendency.
VO2max PRS when present
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
Growth & 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
Detox enzymes
Glutathione and detox-enzyme context. Needs whole-genome CNV/SV reading.
GSTM1/GSTT1 deletion or PRS when present
More than traits. Your genome can place you in reference context.
The full genome gives a broader foundation for comparing your DNA with public reference samples. We can show broad clusters, nearby 1000 Genomes population labels, and the marker-overlap quality behind the result.
The boundary matters: this is not ethnicity, nationality, race, tribe, caste, religion, or a country-of-origin result. It is genetic similarity to reference-panel samples.
Example result wording
Your genome projects closest to the European reference cluster, with nearby reference-panel labels including Iberian, Toscani, and British.
Marker-overlap quality: moderate. This is reference-panel similarity, not an ethnicity or identity label.
Broad cluster
AFR, AMR, EAS, EUR, or SAS reference similarity.
Nearby labels
Groups such as Yoruba, Han Chinese, Bengali, Puerto Rican, Iberian, or Toscani.
Confidence
High, moderate, low, or hidden based on usable ancestry markers.
It reads like a person, not a printout.
Most genetic reports bury the point under jargon. Yours says the thing, then tells you what to do about it. Here's a sample of what opens in your app.
Medications
Clears some types slowly
Worth a conversation with your doctor.
Caffeine
Fast burner
Coffee clears quickly. A second cup is fine.
Vitamin D
Runs low
You likely need more than most.
Recovery
Slower to bounce back
Build extra rest between hard days.
Sleep
Early riser
Your natural clock runs ahead.
Read once. Learn from it for life.
Science keeps figuring out what DNA means. Because we read all of yours, you never have to test again. New findings about vitamin D, sleep, smell, medication response, and recovery can keep reading from the same swab you gave once.
Read once
One cheek swab. We sequence every letter of your DNA, cover to cover.
New answers, no retest
New vitamin D, sleep, medication, smell, or fitness research can read from the same file. You never swab again.
It keeps paying back
The same file powers questions the science hasn't even published yet, the day it can.
The cheapest test you only pay for once.
A basic kit is locked to whatever it measured the day you spat in the tube. Your genome isn't. New nutrition research, new sleep-stage context, new medication signals, a panel that didn't exist yet, all of it reads off the file you already own, with nothing more to buy and nothing more to swab.
Start your file for $349
A better starting point than another guess.
Before the supplements, before the routines, before guessing how your body meets a new medicine, there's your genome. Reading all of it gives you plain genetic context for everyday choices, and useful notes to bring to your doctor when medication questions come up.
One swab, tracked from your door to your results.
Order your kit
Check out through Biome. We place the sequencing order and send your activation details.
Swab and send it back
Register the kit, collect a saliva sample at home, and mail it to the lab. You track every step.
Watch it sequence
Follow the sample from received, to sequencing, to analysis. No black box, no guessing.
Read your answers
Plain-language panels open in the Biome app, with a portable copy of your genome to keep.
Two ways to read your DNA.
Both start with the same easy swab. The difference is how much of you they read, and how long the answers keep coming.
Basic DNA test
$249
- Reads hundreds of thousands of key spots
- Everyday wellness answers on a budget
- Results stay fixed to today's markers
Full genome · recommended
$349
- Reads every letter of your DNA
- The complete picture, read once
- Keeps turning up new answers as science grows
What it can tell you
✓Everything the basic DNA test covers, read with broader, deeper coverage across your whole genome.
✓A stronger foundation for how your body handles medications, including PGx and emerging medication-response context to review with a clinician.
✓Food, vitamins, sleep, smell, taste, training, recovery, hormone, skin, and longevity context, all written in plain language.
✓Genome-wide ancestry reference context, shown as similarity to public reference groups rather than ethnicity or nationality.
What it won't
It doesn't diagnose disease or replace a clinical genetic test.
It doesn't prescribe supplements, medications, peptides, or doses.
It can't promise that every possible risk or variant is caught, interpreted, or actionable today.
Read your DNA once. Learn from it for the rest of your life.
Every letter of your DNA, sequenced cover to cover, turned into plain answers you can act on. One swab, far less than a private workup, and nothing more to buy.
Good questions, answered.
The details behind the swab, the science, and what you walk away with.
Order your kitThese results describe inherited tendencies and medication-response context. They're educational. They are not a diagnosis, a treatment plan, dosing instructions, or a substitute for clinician review. The genome can surface medically relevant findings, but interpreting them takes qualified clinical review, and not every risk or variant will be caught or actionable today.