Biocodify

The simplest way to explore genetic data

Upload your raw DNA file. See your variants annotated with clinical significance, population frequencies, and gene information.

Get Started See how it works

Variant Browser

4,234,891 total variants, 47,392 with ClinVar annotation

Active filters: Pathogenic ClinVar only Rare (<1%)
47 results (filtered) Showing 1-10 of 47
chr17
43,094,464
rs80357906
Het
0.0001
BRCA1
Pathogenic
Hereditary breast and ovarian cancer
chr19
11,224,088
rs28942078
Het
0.0003
LDLR
Pathogenic
Familial hypercholesterolemia
chr3
38,589,553
rs199473146
Het
0.0002
SCN5A
Pathogenic
Long QT syndrome
chr7
117,559,593
rs113993960
Hom
0.0108
CFTR
Pathogenic
Cystic fibrosis
chr6
26,093,141
rs1800562
Het
0.0412
HFE
Pathogenic
Hereditary hemochromatosis
Page 1 of 5

Works with data from

23andMe Ancestry DNA Nebula Genomics Family Tree DNA MyHeritage Sequencing.com Nucleus Genomics
Any VCF Any 23andMe-like TXT

All company names are trademarks of their respective owners. Biocodify is not affiliated with or endorsed by these companies.

.vcf

whole_genome.vcf

847 MB • 4.2M variants

##fileformat=VCFv4.2

#CHROM POS ID REF ALT QUAL ...

chr1 10177 rs367896724 A AC

chr1 10352 rs555500075 T TA

chr1 10616 rs376342519 C CG

chr1 13110 rs540538026 G A

chr1 13116 rs62635286 T G

...

+ 4,234,891 more rows

Unused
Hard to read
rs367896724 what's this?

4.2M variants

hidden in plain text

No annotations

Your genetic data is just sitting there

You paid for a DNA test. You got some ancestry results and a few trait reports. But your raw data file contains millions of data points that consumer tests don't show you.

The problem? Exploring raw genetic data requires clunky tools with steep learning curves and outdated interfaces.

How It Works

Finally, a beautiful way to explore your variants

Get Started in 3 Easy Steps

No PhD required.

1. Upload

Drag and drop your raw data file. We support VCF, 23andMe, Nebula, Ancestry, and more.

2. Annotate

Every variant is enriched with ClinVar classifications, gnomAD frequencies, and gene information.

3. Explore

Filter and browse your variants in a clean, modern interface by gene, significance, or frequency.

Who is Biocodify for?

For the curious

"I want to see what's actually in my raw data file. All of it, not a curated selection."

For the data-driven

"I want my variants annotated with real database references, not just consumer-friendly summaries."

For genetic counselors

"I need a faster way to preview client data with ClinVar annotations before our sessions."

Powerful Browsing Tools

Explore your data your way

Three specialized browsers to help you understand your genetic data from different angles.

Variant Browser
Pathogenic ClinVar Rare
rs80357906 Pathogenic

chr17:43094464 · BRCA1 · Breast cancer

rs113993960 VUS

chr7:117559593 · CFTR · Cystic fibrosis

Explore millions of variants

Browse through all your genetic variants with powerful filtering and sorting capabilities.

Filter by clinical significance (Pathogenic, Benign, VUS)
Search by rsID, gene, or genomic position
Sort by population frequency or clinical importance
Always Up To Date

Stay current with ClinVar updates

ClinVar releases new data monthly. We automatically re-annotate your variants and notify you when classifications change.

Automatic monthly ClinVar sync
Email notifications for classification changes
Track upgrades and downgrades over time
No need to re-upload your data
ClinVar Updates
Latest version: 2026-01 Synced
Classification Changed BRCA1
VUS Benign
New Annotation CFTR
No data Pathogenic
No Sign Up Required

See it for yourself

Explore a real variant analysis with ClinVar annotations, gene information, and population frequencies. All in under 30 seconds.

Explore the Demo
Privacy First

Your data stays yours

We take privacy seriously. Your genetic information is protected at every step.

Encrypted storage

Your genetic data is encrypted at rest and in transit using industry-standard protocols.

One-click delete

Remove all your data permanently anytime from your account settings. No questions asked.

Never sold

We don't sell, share, or monetize your genetic data. Ever. Your data is yours alone.

Your raw data, finally readable.

Upload your file and start exploring your variants.

Get Started

Frequently
asked questions

Is my data safe?

Yes. Your genetic data is encrypted at rest and in transit. We never share or sell your data. You can delete everything with one click.

What file formats do you support?

We support raw data exports from 23andMe, Nebula Genomics, Sequencing.com, Nucleus Genomics, Ancestry DNA, MyHeritage, ftDNA and standard VCF files. Do you have something else? Contact us! We would love to support.

How is this different from my 23andMe results?

23andMe shows you a curated subset of your data with their own interpretations. Biocodify lets you explore your complete raw data annotated against public databases like ClinVar and gnomAD.

What if a classification changes in ClinVar?

We re-annotate your data when ClinVar updates (typically monthly). If any classifications change, we'll notify you.

Is this a diagnostic tool?

No. Biocodify is for educational and informational purposes only. It is not intended to diagnose, treat, or prevent any condition. Consult a qualified professional for interpretation.