--- title: "Dante Labs | Clinical Genomic Testing for Your Health" description: "Clinical-grade genetic testing from an accredited lab. Read your genome once, track your cellular health over time and share every report with your doctor." url: "https://dantelabs.com/" --- CLIA/CAP Lab # Special Singles Day Campaign: 30% Off The answer is in your genome. The complete picture of your genetic health. Clinical grade sequencing and personalized, actionable reports updated as science evolves. [Sequence your genome](https://dantelabs.com/order) - CLIA Certified - CAP Accredited - ISO 15189 Medical Lab - ACMG Classified - HIPAA & GDPR - 100,000+ Genomes Sequenced * ![Nature](https://dantelabs.com/cdn/images/k5ybuy00/production/be1cc27ab0904412c830d1d8a5501403da516c80-131x32.svg) * ![NVIDIA](https://dantelabs.com/cdn/images/k5ybuy00/production/4f3f9df038b8d1a1b0371bfb056e0530aa19c5a8-656x120.svg) * ![CNN](https://dantelabs.com/cdn/images/k5ybuy00/production/fa116019ea01ff2fef711815db73632e722cfa75-1000x476.svg) * ![CNBC](https://dantelabs.com/cdn/images/k5ybuy00/production/a3bd43d652304b3ea962bf48cbc0a6c279169773-41x31.svg) * ![AWS](https://dantelabs.com/cdn/images/k5ybuy00/production/0efc08f7d2390100e801d656b977f5c08bc2e273-304x182.svg) * ![Financial Times](https://dantelabs.com/cdn/images/k5ybuy00/production/323bdd4d7017413a9a54a0f86be7fd7ef9c7af3a-982x283.svg) * ![ASHG](https://dantelabs.com/cdn/images/k5ybuy00/production/9a4a10828ac3bb0e60a78f1e997aa237069f4c06-203x46.svg) * ![HIMSS](https://dantelabs.com/cdn/images/k5ybuy00/production/a72ccd14a630e36e3012c1305ef33b00ea55e418-561x183.svg) ## One letter in 6.4 billion. Consumer DNA chips read fewer than 0.02% of them, so a discovery anywhere else never reaches their reports. We read every one, so each new finding can be checked against your whole genome. [Conditions we report on →](https://dantelabs.com/conditions) ## Your DNA never changes. What it can tell you does. A complete record that belongs to you, updated every time the science moves. [Sequence your genome](https://dantelabs.com/order) The Most Comprehensive Genome Analysis ## We report the science, not just the result. 01Proactive advice A result turned into something to do, with the study it rests on. [See the conditions we report on →](https://dantelabs.com/conditions) [Already Tested Most consumer DNA tests read less than 0.02% of your genome. We read all of it. See what it missed →](https://dantelabs.com/upgrade) Proactive advice CYP1A2 · rs762551 · C/C ### Caffeine metabolism Slow metaboliser Your move Last coffee by 14:00. Your liver clears caffeine slowly, so an afternoon cup is more likely to cost you deep sleep and push up your blood pressure. An espresso at 15:00 is still working at midnight. Fast You From your Nutrigenetics report [Cornelis et al., JAMA 2006](https://pubmed.ncbi.nlm.nih.gov/16522833/) ### Hereditary haemochromatosis HFE · p.Cys282Tyr · Homozygous Pathogenic A pathogenic missense variant in HFE, on both copies of the gene. The change sits in exon 4, at the base marked on the gene below. 5′ 3′ 123456 chr6:26,087,509–26,098,571 (GRCh37) · 6 exons · 11.1 kb Explain in plain EnglishAugmented with AI Classified against ACMG guidelines CFTR · MONDO:0009061 ### Cystic fibrosis Autosomal recessive Carrier CFTR Heterozygous Pathogenic c.1521_1523del · p.Phe508del You carry one altered copy. Recessive conditions usually only show up when both copies are affected, so this alone does not typically cause disease, but your children could inherit it. ### Breast cancer PRS313 · z = +0.11 Higher than 54 in 100 people 30X · GRCh37 ### Your whole genome, as files Yours to keep 98 GB in your BAM file alone - DL52914.bam Aligned reads 98.4 GB - DL52914_1.fq.gz Raw reads 42.1 GB - DL52914_2.fq.gz Raw reads 43.7 GB - DL52914.vcf.gz Variants 148 MB Standard formats any genomics tool can open BAM · FASTQ · VCF Who We Help ## Every genetic question deserves a complete answer. Whether you are looking for answers today or protecting your health for tomorrow, a complete read of your entire genome is the only place to start. [Proactive Health](https://dantelabs.com/who-we-help/proactive) ### [You want to know before something forces the question.](https://dantelabs.com/who-we-help/proactive) [Whole genome sequencing gives you the complete genetic picture now — so you and your doctor can decide before anything becomes urgent.](https://dantelabs.com/who-we-help/proactive) [Learn more](https://dantelabs.com/who-we-help/proactive) [Hereditary Risk](https://dantelabs.com/who-we-help/hereditary-risk) ### [It runs in your family. Now you can know if it runs in your genes.](https://dantelabs.com/who-we-help/hereditary-risk) [Your genome contains inherited variants associated with cardiac, cancer and neurological conditions. We read all of them — with the clinical depth to give the result meaning.](https://dantelabs.com/who-we-help/hereditary-risk) [Learn more](https://dantelabs.com/who-we-help/hereditary-risk) [Unexplained Symptoms](https://dantelabs.com/who-we-help/undiagnosed) ### [When traditional lab tests say you're fine. And you know you're not.](https://dantelabs.com/who-we-help/undiagnosed) [Standard diagnostic tests check for a pre-selected set of answers. We sequence your full DNA — including the parts no test was designed to check.](https://dantelabs.com/who-we-help/undiagnosed) [Learn more](https://dantelabs.com/who-we-help/undiagnosed) [Treatment Not Working](https://dantelabs.com/who-we-help/treatment-not-working) ### [Your diagnosis may be right. Your treatment plan may be incomplete.](https://dantelabs.com/who-we-help/treatment-not-working) [Your genes determine which treatments are most likely to work — and which are not. We give your doctor the evidence to inform your plan.](https://dantelabs.com/who-we-help/treatment-not-working) [Learn more](https://dantelabs.com/who-we-help/treatment-not-working) ![The Dante Labs whole genome sequencing collection kit](https://dantelabs.com/cdn/images/k5ybuy00/production/2147f4e99dd00de4cd7e264bac04541cb43b3849-1400x1082.jpg?w=1000\&q=70\&fm=webp\&fit=max) DANTE GENOME TEST ## Your complete genome. Sequenced once, yours for life. A single sample, collected at home. Your whole genome is sequenced at 30X in accredited laboratories and held as a permanent record - every new report the science produces is read from it, without a second test. From $314.30 Was $449 [Sequence your genome](https://dantelabs.com/order) Free shipping. CLIA and CAP certified. Privacy first Accredited laboratories · Reports updated as the science advances · Your data is always yours ## They give you the sketch, we give you the full picture. Consumer genotyping chips read under 0.02% of your genome. We sequence all of it at 30X depth in accredited laboratories, which is what makes a variant a finding a clinician can act on. 30X Coverage gold standard 5M Variants identified per test 830+ Clinical grade reports 99.98% Sequencing accuracy Accredited by & published in Clinical Laboratory Improvement Amendments College of American Pathologists American Society of Human Genetics Nature International Society for Cell & Gene Therapy Gene Journal [See outcomes →](https://dantelabs.com/outcomes) ![A newborn baby asleep on a knitted blanket](https://dantelabs.com/cdn/images/k5ybuy00/production/7dfed64352a63e26f14036d46c21dd0ec5f15487-2400x1600.jpg?w=1600\&q=70\&fm=webp\&fit=max) Hereditary screening ## Tested now, for them. Hereditary conditions travel down families. Whether you're planning a family or already have one, reading your whole genome shows what could be passed on, so the next generation starts with answers rather than surprises. ### Hereditary cancer - [Hereditary Breast and Ovarian Cancer (BRCA1/2)](https://dantelabs.com/conditions/hereditary-breast-ovarian-cancer) - [Lynch Syndrome](https://dantelabs.com/conditions/lynch-syndrome) - [Li-Fraumeni Syndrome With Premium](https://dantelabs.com/conditions/li-fraumeni-syndrome) - [Hereditary Diffuse Gastric Cancer With Premium](https://dantelabs.com/conditions/hereditary-diffuse-gastric-cancer) - [Colorectal Cancer & Polyposis With Premium](https://dantelabs.com/conditions/colorectal-cancer-polyposis) ### Inherited heart conditions - [Hypertrophic Cardiomyopathy With Premium](https://dantelabs.com/conditions/hypertrophic-cardiomyopathy) - [Long QT Syndrome With Premium](https://dantelabs.com/conditions/long-qt-syndrome) - [Familial Hypercholesterolemia](https://dantelabs.com/conditions/familial-hypercholesterolemia) ### Passed on by healthy parents - [Cystic Fibrosis](https://dantelabs.com/conditions/cystic-fibrosis) - [Spinal Muscular Atrophy](https://dantelabs.com/conditions/spinal-muscular-atrophy) - [Sickle Cell Disease](https://dantelabs.com/conditions/sickle-cell-disease) [Test your whole genome](https://dantelabs.com/order) [See every condition we cover →](https://dantelabs.com/conditions) [Hereditary risk →](https://dantelabs.com/who-we-help/hereditary-risk) In Their Words ## Everyone starts with a different question. A family history of cancer. A diagnosis no one could explain. A family on the way. Hear why they chose to read their whole genome, not a sample of it. Every Year ## Your genome becomes more valuable every year. Your DNA does not change, but what science knows about it does. As each new finding is published, we check it against the sequence you already gave us and turn it into new insight in your reports — no new sample, no second test. [How whole genome sequencing works →](https://dantelabs.com/whole-genome-sequencing) The Process ## No clinic visits. Everything from home. ### Order your kit Free delivery worldwide. ### Collect your sample Simple saliva collection at home. Takes 5 minutes. Everything you need is in the kit. ### Send it back Pre-paid return label included. Drop it in any post box. ### Access your results Reports delivered to your Genome Manager in 6–8 weeks. Review every finding and share directly with your physician. [Optional add-on](https://dantelabs.com/membership) ### [Track what's changing](https://dantelabs.com/membership) [Not part of the genome test. A separate membership that sends a blood spot card twice a year, showing what is changing at the cellular level — which your genome never does.](https://dantelabs.com/membership) [Cellular Monitoring →](https://dantelabs.com/membership) > “They never added the numbers up until now, when they saw the Dante Labs report.” > > Thomas, Scotland > > Queen Elizabeth University Hospital Glasgow > > Years of specialist referrals found nothing. A single whole genome test identified Noonan Syndrome and RUNX1 deficiency, both accepted by NHS genetics. > > [Read the full case and its disclosure →](https://dantelabs.com/outcomes#thomas) Whole Genome Sequencing From $314.30 Was $449 Whole genome at 30X, sequenced once and yours for life 90+ personalised clinical reports covering core hereditary risks and proactive health and 30+ risk scores included. [760+ personalised clinical reports covering core hereditary risks and proactive health and 60+ risk scores with Premium: $69.30 for the first year, then $99 a year](https://dantelabs.com/order?tier=premium). Free shipping. CLIA and CAP certified. Privacy first ### Everything in Premium + AI - 760+ personalised clinical reports covering core hereditary risks and proactive health - 60+ risk scores - 30x whole genome sequencing - GRCh38 alignment - Raw data (BAM, FASTQ and VCF) - Complete ancestry: maternal & paternal lines, regional mix - Your data is never shared or sold - Carrier screen for family planning - Personalised monthly insights - Dante Chat with AI Insights - Integrate your genome with AI via MCP support - Weekly updates [Order your kit](https://dantelabs.com/order) [→](https://dantelabs.com/membership) CLIA Certified CAP Accredited ISO 15189 Medical Lab ACMG Classified HIPAA & GDPR 100,000+ Genomes Sequenced As seen in & research partnerships ![Nature](https://dantelabs.com/cdn/images/k5ybuy00/production/be1cc27ab0904412c830d1d8a5501403da516c80-131x32.svg) ![NVIDIA](https://dantelabs.com/cdn/images/k5ybuy00/production/4f3f9df038b8d1a1b0371bfb056e0530aa19c5a8-656x120.svg) ![CNN](https://dantelabs.com/cdn/images/k5ybuy00/production/fa116019ea01ff2fef711815db73632e722cfa75-1000x476.svg) ![CNBC](https://dantelabs.com/cdn/images/k5ybuy00/production/a3bd43d652304b3ea962bf48cbc0a6c279169773-41x31.svg) ![AWS](https://dantelabs.com/cdn/images/k5ybuy00/production/0efc08f7d2390100e801d656b977f5c08bc2e273-304x182.svg) ![Financial Times](https://dantelabs.com/cdn/images/k5ybuy00/production/323bdd4d7017413a9a54a0f86be7fd7ef9c7af3a-982x283.svg) ![ASHG](https://dantelabs.com/cdn/images/k5ybuy00/production/9a4a10828ac3bb0e60a78f1e997aa237069f4c06-203x46.svg) ![HIMSS](https://dantelabs.com/cdn/images/k5ybuy00/production/a72ccd14a630e36e3012c1305ef33b00ea55e418-561x183.svg) ## Your genome, sequenced properly. Once. Premium access with 830+ actionable, physician-ready reports, on hereditary risk, drug response and carrier status and every new report the science produces, for as long as you hold the data. [Order your kit](https://dantelabs.com/order) [Discover Transcriptomics Cellular Monitoring](https://dantelabs.com/rna) CLIA Certified CAP Accredited ISO 15189 Medical Lab ACMG Classified HIPAA & GDPR 100,000+ Genomes Sequenced