genome

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Genomegenome
AI vs Clinical Analysis

I uploaded my DNA to ChatGPT. Here's why that's a terrible idea.

A Reddit post with +294 upvotes showed someone generating a 100-page DNA report with ChatGPT. It looked impressive. It was also full of hallucinated findings, fabricated citations, and zero clinical validation.

Cross-checked with the latest researchZero hallucinationsYour DNA is deleted after analysis
The Problem

Why ChatGPT can't analyze your DNA

Large language models generate text. They don't query medical databases, score genetic markers, or understand genomic sequences.

It hallucinates on genetic data

ChatGPT doesn’t access ClinVar, PharmGKB, or any medical database. It guesses based on training data that may be outdated or wrong.

It can’t score variant pathogenicity

LLMs don’t understand DNA sequences. They process text. Our AI, trained on 8.8 trillion DNA sequences, actually reads DNA.

It stores your genetic data

Your DNA file goes to OpenAI’s servers. You have no control over how it’s used, retained, or who accesses it.

It gives you false confidence

A 100-page ChatGPT report looks impressive. But when 30% of findings are hallucinated, it’s worse than no report at all.

Get real DNA analysis. Zero hallucinations.

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Side by Side

Same variant. Very different answers.

Here's what happens when you ask about MTHFR C677T — one of the most commonly searched genetic variants.

ChatGPT response

Unverified output

Based on your rs1801133 variant, you may have a reduced ability to process folate.

This is sometimes associated with higher homocysteine levels.

However, I cannot verify this against clinical databases.

Please consult a healthcare professional for accurate interpretation.

No source citations
No risk classification
No population frequency
Generic disclaimer

genome report

Sourced from ClinVar
Variantrs1801133 (MTHFR C677T)
ClassificationWell-established risk factor
Your genotypeCT (heterozygous carrier)
Population freq.34% of Europeans carry this variant
SourceClinVar RCV000003164 • PMID: 9545397
ActionDiscuss methylfolate supplementation with your doctor
Every finding sourced
Population frequency included
Actionable recommendations
Reproducible results
Comparison

genome vs AI chatbots

General-purpose AI is powerful for many things. Genetic analysis is not one of them.

Medical databases

genome: 15 medical sources (ClinVar, PharmGKB, GWAS…)
ChatGPT: None

Variant scoring

genome: CADD, REVEL, AlphaMissense, SpliceAI
ChatGPT: Cannot score variants

Source citations

genome: PMID, ClinVar ID on every finding
ChatGPT: Often fabricated

Pharmacogenomics

genome: 672 drugs, doctor-ready guidelines
ChatGPT: General advice only

Privacy

genome: Zero data retention
ChatGPT: Data stored on OpenAI servers

Accuracy

genome: Deterministic, reproducible
ChatGPT: Hallucinations common

Your DNA deserves better than a chatbot.

Medical-grade analysis from 15 medical sources, not training data.

Get Started
How It Works

Three steps to real answers

1

Upload your DNA file

23andMe, AncestryDNA, Nebula, MyHeritage, or any VCF file. It takes 30 seconds.

2

We cross-reference 15 medical sources

ClinVar, PharmGKB, GWAS Catalog, gnomAD, and 11 more. Every finding is sourced. Not a chatbot — a medical-grade analysis built by geneticists.

3

Get your sourced report

Health insights, pharma compatibility, risk timeline, and actionable recommendations. Every claim linked to its source.

Genome analysis pipeline visualization

Our pipeline cross-references your DNA with 15 medical sources in real-time — not a chatbot conversation

What People Say

The internet is learning the hard way

Real posts from people who tried using AI chatbots for DNA analysis.

I uploaded my 23andMe raw data to ChatGPT and got a 100-page report. Impressive looking… until I cross-referenced with ClinVar and found half the citations didn’t exist.

r/biohackers

+294

ChatGPT told me I had a ‘high risk’ BRCA variant. Panicked for a week. Turns out the variant doesn’t even exist in ClinVar. Complete hallucination.

r/genomics

+47

Using my DNA, health reports and LLMs I built a personalized supplement stack. But you CANNOT trust the LLM output without cross-referencing every single claim.

r/biohackers

+26

2.6M

genetic markers checked

15

medical sources

0

hallucinations

€99

one-time payment

FAQ

Common questions

Real DNA analysis.
Zero hallucinations.

Unlike ChatGPT, every finding is sourced from ClinVar, PharmGKB, and peer-reviewed research. No hallucinations, no guessing.

2,400+ reports generated