Open beta · free while it lasts

Your genetics,
read honestly.

Kardi reads your genetic profile before it goes looking for research, then answers in plain language with every source shown. When the evidence is not there, it says so instead of guessing.

For wellness and education. Not a diagnosis, and never a substitute for your doctor. 18+.

How it works

Context first. Then the search.

Most health tools search your question. Kardi searches your question and your genotype, so a general answer becomes one that actually applies to the body reading it.

01

Build a profile

Enter the variants you already know, or bring the raw file from a consumer test. Each person in the household gets their own profile with their own genes, markers, and daily protocol.

02

Ask in plain language

"Why am I so tired in the afternoon." No jargon required. Kardi expands that into the queries a researcher would actually run, using the variants on the profile to aim them.

03

Get a cited answer

Every claim traces back to a source you can open and read. Take it to your doctor as a starting point for a conversation, which is exactly what it is built to be.

The honest part

It will tell you when it does not know.

The wellness internet is confident about everything. Kardi is built the other way around. Answers are assembled only from verified facts, and anything that cannot be traced to a source gets refused rather than invented.

ANSWEREDMTHFR C677T and homocysteine?

Carrying one copy of C677T is associated with reduced enzyme activity, and reduced activity is associated with higher circulating homocysteine. A homocysteine panel is the marker that would show whether that pattern is present for you.

Cited research
Frosst et al., Nature GeneticsPMID: 7647779
Jacques et al., CirculationPMID: 8635391
REFUSEDWill this supplement cure my fatigue?

I do not have a verified source that supports an answer here, so I am not going to give you one. Nothing in the fact store connects that supplement to that outcome at a strength worth repeating.

Here is what I can show you from your profile, and the question worth bringing to your clinician instead.

Coverage

Starting with the genes that change daily life.

Methylation, catecholamine clearance, histamine breakdown, detox capacity, and vitamin D handling. The small set with the largest lived effect, each with its own activity read, symptom pattern, nutrient support, and the lab marker that confirms it.

MTHFR C677T
MTHFR A1298C
COMT V158M
DAO AOC1
MAOA
GSTM1
NQO1
VDR Taq
Privacy

The most personal data you own.

Your genome cannot be changed, reissued, or taken back once it is out. So the safest place to keep it is the one place nobody can buy it from.

What Kardi does

  • Keeps your genetic profile on your own device by default
  • Sends only the specific variants a question needs, never a whole file
  • Shows the source behind every claim so you can check the work
  • Lets you export or delete everything, in one click, at any time

What Kardi will never do

  • Sell, license, or share your data with anyone, ever
  • Hand it to an insurer, an employer, or a data broker
  • Sell you the supplements it tells you about
  • Train a model on your genome

Where the line is

Kardi is a general wellness tool. It supports and informs. It does not diagnose, treat, cure, or prevent any disease, and it is not a medical device. Nothing here replaces your physician. Bring what you find to them.

Open beta

Your genome deserves a reader it can trust.

Every account is free during the beta. Your data is encrypted on your device before it leaves, sealed with a key only you hold.