Codon

The science behind the answers

Codon doesn't let the model free-associate about your DNA. Every answer is grounded in a curated evidence base drawn from open scientific sources — and the model is instructed to reason strictly from it and never invent a locus.

ClinVar

NIH's public archive of variant–condition relationships. Source for carrier and clinical-significance calls.

PharmGKB / CPIC

The pharmacogenomics knowledge base and clinical dosing guidelines (clopidogrel, warfarin, statins, codeine).

SNPedia

Community-curated SNP encyclopedia for well-replicated traits and common variants.

How grounding works

  • 1. A client-side router maps your question to the relevant loci and pulls just those genotypes from your in-browser file.
  • 2. Matching evidence entries (rsid, gene, genotype→effect table, citation) are sent alongside.
  • 3. The counselor must match your actual genotype to the right effect row, distinguish association from destiny, and stay non-prescriptive.
  • 4. If your chip didn't test a position, it says so honestly instead of guessing.

What Codon covers today

22 curated variants

A focused, high-value set — the topics people actually search for — rather than a 20,000-row dump. Expanding over time.

Pharmacogenomics

Clopidogrel (Plavix) & CYP2C19

How you activate clopidogrel — a pro-drug your CYP2C19 enzyme must switch on.

rs4244285rs4986893rs12248560

Warfarin (Coumadin) dosing

Your CYP2C9 + VKORC1 genotype, the basis of genotype-guided warfarin dosing.

rs1799853rs1057910rs9923231

Statins & muscle pain (SLCO1B1)

Your risk of statin-induced muscle aches, driven by the SLCO1B1 transporter.

rs4149056

Codeine, tramadol & CYP2D6

How you metabolize codeine/tramadol and many antidepressants via CYP2D6.

rs3892097

Health signals

MTHFR & folate

Your MTHFR C677T status — and why it's far less dramatic than the internet says.

rs1801133

Type 2 diabetes (common variants)

Two well-replicated common variants nudging type 2 diabetes risk up or down.

rs7903146rs1801282

APOE & Alzheimer's

Your ε2/ε3/ε4 status — the strongest common genetic factor for late-onset Alzheimer's.

rs429358rs7412

Traits

Caffeine metabolism

free

Whether you're a fast or slow caffeine metabolizer (CYP1A2).

rs762551

Alcohol flush reaction

free

The ALDH2 'Asian flush' variant — and its esophageal-cancer caveat.

rs671

Taste: bitter & cilantro

free

Whether cilantro tastes soapy and how strongly you taste bitter foods.

rs1726866rs72921001

Nutrition

Lactose tolerance

Your lactase-persistence variant — can you digest dairy as an adult?

rs4988235

Carrier status

Cystic fibrosis carrier

The most common CF mutation (F508del) — relevant for family planning.

rs113993960

Sickle cell trait

Sickle cell carrier / trait status (HbS).

rs334

Hemochromatosis (iron overload)

HFE iron-overload variants C282Y & H63D — often checkable with a simple blood test.

rs1800562rs1799945

Important. Codon is an educational tool that helps you interpret raw genetic data you already own. It is not a medical device and does not diagnose, treat, or prevent any condition. Genetic associations describe probabilities across populations, not your destiny. Always talk to a qualified clinician or genetic counselor before making any health decision.