Privacy-First

Understand your genome — privately and in minutes

Match your genome against 4.2 million ClinVar is a public database from the U.S. National Library of Medicine that explains how genetic variants may relate to health. variants — including pathogenic markers — privately on your own computer.

Supports genome files from

Supports genome files from

Zero Data Transmission
4.2M ClinVar Variants
Whole Genome in Under 5 Min
NCBI ClinVar (Public Domain)

How It Works

Three steps. Under five minutes from download to your first report. Everything stays on your computer.

1

Install & Activate

Download for macOS or Windows, enter your license key, and BioDecode automatically downloads and builds the ClinVar database. One-time setup, about 60 seconds.

2

Drop Your Genome File

Drag your genome file into the app (VCF, TXT, CSV, TSV, GZ, or ZIP). BioDecode parses variants and automatically matches them against 4.2 million ClinVar entries — all locally.

No genome file yet? See your options ↓

3

View & Export Your Report

Your interactive report appears right in the app. Copy findings or save as PDF in one click so you can paste into ChatGPT or any LLM, or share with your doctor.

Don't Have a Genome File Yet?

BioDecode analyzes a genome file you already own. If you're not sure what you have — or don't have one yet — start here.

Already tested with 23andMe, Ancestry, Nebula, or similar?

You likely already have what you need. Most providers let you download your raw data or sequencing files from your account settings in a few minutes — no new test required.

If it came from an ancestry-style kit
23andMe, Ancestry, MyHeritage and FamilyTreeDNA read a genotyping array — roughly 640,000 pre-selected positions, a fraction of 1% of your ~3 billion base pairs. BioDecode checks every one of them, but it can only see the positions your kit tested. For full coverage, consider whole genome sequencing
If it came from whole genome sequencing
Nebula, Dante Labs, Sequencing.com or a clinical lab already give you virtually your entire genome — nothing further to buy. Load your VCF and BioDecode reads its supported variant records locally.
How to download your raw data

Never had your DNA sequenced?

Consider 30x whole genome sequencing. It reads virtually your entire genome — millions more positions than an ancestry test kit — giving BioDecode far more of your DNA to check against ClinVar. Sequencing.com offers whole genome sequencing, including an expedited option, and lets you download your genome data files to analyze locally.

What you get back
Your own genome data files, covering virtually all ~3 billion base pairs rather than a pre-selected 640,000. They're yours to keep and re-run locally — ClinVar grows every month, and a file you already own can be checked against it again for free.
Get Whole Genome Sequencing

Affiliate disclosure: BioDecode may earn a commission if you buy through this Sequencing.com link. Sequencing.com is an independent company with its own terms and privacy policy.

Built for Privacy. Built for Science.

Every design decision prioritizes your data security and scientific accuracy.

Zero Data Transmission

Your genomic data never leaves your device. No servers, no cloud, no API calls with your genetic information. Everything runs locally.

Scientifically Curated Database

Powered by ClinVar, a curated database maintained by the U.S. National Center for Biotechnology Information (NCBI) — the gold standard for variant classification.

Whole Genome in Under a Minute

Parses 4.7M+ variants and cross-references the complete ClinVar database in under 60 seconds. No waiting for cloud servers.

Share Insights Safely

Easily copy findings or save as PDF for personal use, then paste into ChatGPT or any LLM, or share with your healthcare provider.

Comprehensive Categorization

Pathogenic and likely pathogenic findings flag known disease-linked variants. VUS means uncertain significance (not enough evidence yet). Drug response shows variants that may affect medication response, and risk factors show variants associated with increased risk. Every finding includes ClinVar star ratings and source links.

Buy Once, Own Forever

No subscriptions, no per-report fees. One-time purchase for macOS and Windows. Update the ClinVar database anytime from the free NCBI source.

Why Privacy Matters for Genomics

Your DNA is not just data — it's the most personal information that exists.

Uniquely Identifying

Even a small set of genetic variants can uniquely identify you. Unlike a password, you can never change your DNA. Once genomic data is exposed, it's exposed permanently.

Family Implications

Your genetic data reveals information about your parents, siblings, and children. Sharing your genome doesn't just affect you — it has implications for your entire family.

Health Predispositions

Genomic data can reveal predispositions to diseases, carrier status, and drug sensitivities. This information could be used against you by insurers or employers if it falls into the wrong hands.

The BioDecode Promise

BioDecode is built on privacy by design. Your genome file is processed entirely on your machine. We have no servers that receive, store, or process your genomic data. There is no account creation, no telemetry, and no network calls with your data. The application works fully offline after initial setup.

Why we chose local-first analysis

Many DNA services ask you to upload your genome to cloud servers you do not control. If those companies are acquired or policies change, your data may be exposed to new risks. BioDecode avoids that model: analysis runs locally on your computer, so your genomic data stays with you.

Read our full privacy story

Get BioDecode

One-time purchase. No subscription. No per-report fees. Your data stays yours, forever.

🌱 Spring Offer
$99 $49 one-time purchase — no subscription needed
Offer ends in:

Secure checkout powered by Stripe. License key and download links are delivered instantly by email.

You'll need a raw DNA or genome file to analyze. Don't have one yet?

Example report

Example Analysis Report

Input
genome.vcf.gz
Variants read
4,763,005
ClinVar matches
47,330
Reference
GRCh38
ClinVar data built
2026-08-04
Engine
1.5.0

Classifications are reproduced as published by their submitters. BioDecode adds no clinical interpretation.

Part 1 · ClinVar record
8 Pathogenic 3 Likely pathogenic 57 Risk factor 52 Drug response 324 Uncertain significance 41,857 Benign / likely benign
GeneVariantGenotypeClassificationReview statusCondition(s)ClinVar
BRCA1chr17:43071077A>GHeterozygousPathogenic★★★☆reviewed by expert panelHereditary breast-ovarian cancer syndrome +2 relatedVCV000017694
LDLRchr19:11224088G>AHeterozygousLikely pathogenic★★☆☆criteria provided, multiple submittersFamilial hypercholesterolemiaVCV000226352
RYR1chr19:38968314A>GHeterozygousLikely pathogenic★★☆☆criteria provided, multiple submittersMalignant hyperthermia susceptibilityVCV000133027
CDKN2Bchr9:22009312C>THomozygousRisk factor★☆☆☆criteria provided, single submitterMelanoma-pancreatic cancer syndrome with CDKN2B-AS1VCV000523504
CFTRchr7:117559593T>GHeterozygousUncertain significance★☆☆☆criteria provided, single submitterCystic fibrosis spectrum conditionVCV000053313

By condition area — cardiovascular (14) · cancer predisposition (9) · metabolic (7) · neurologic (5)

Part 2 · Curated panels

Published pharmacogenomic, trait and nutrition associations, kept separate from the ClinVar record above.

Pharmacogenomics — 11 genes
GeneGenotypePhenotypeBasisGuideline drugs
CYP2C19*1/*2Intermediate metabolizerObservedclopidogrel, escitalopram +6
SLCO1B1*1/*5Decreased functionObservedsimvastatin, atorvastatin
TPMT*1/*1Normal metabolizerInferred from absence†azathioprine, mercaptopurine
DPYDActivity score 2.0Normal metabolizerInferred from absence†fluorouracil, capecitabine

† Not probed by this file. Reported using the assumed-reference convention, not a positive observation.

Trait & wellness markers — 11
ALDH2 rs671 · typical acetaldehyde clearance ACTN3 rs1815739 · both fast- and slow-twitch isoforms PER3 rs57875989 · no strong chronotype association
Nutrition & metabolism — 7
MTHFR rs1801133 · reduced enzyme activity reported LCT rs4988235 · lactase persistence associated GC rs2282679 · lower vitamin D binding reported
Checked against the 84 “worth knowing” genes

Medical geneticists keep a list of 84 genes (the ACMG secondary findings list, v3.3) where a serious variant is considered worth acting on — even if you were looking for something else entirely. Nothing pathogenic or likely pathogenic turned up in yours. Your file only reads 71 of those 84 genes, though, so the other 13 were never checked. This is not an all-clear.

Restricted results 1 result withheld. Findings for conditions with limited actionability (for example APOE and late-onset Alzheimer’s) are computed but withheld until you ask for them. Display withheld results

Methodology, scope & limitations — sources, coverage, and what BioDecode does and does not do are set out in full at the end of every report.

Every finding in the real app links back to its ClinVar record.

Feel free to write to us with any questions or feedback you may have. We strive to get back to you within 24 hours.