Already have your DNA data? Read it for nutrition.
Upload your 23andMe or AncestryDNA raw file. We read your nutrition-relevant genetics, like MTHFR methylation, in plain language, in your browser. The file never leaves your device.
Sample readIn your browser
C677T, one copy foundMay lower folate activation
A1298C, clearNo variant detected
Review with your clinicianFolic acid vs. methylfolate
Processed on your device. No account needed to read it.
Read your file
Your file is parsed locally and never uploaded or stored. No DNA test yet? AncestryDNA is about $99 and gives you the file. The methylation read here is free.
What it readsA nutrition genetics panel across about 30 well-studied variants, grouped into methylation (MTHFR, MTR, MTRR and more), neurotransmitters, vitamins and minerals, fats and omega-3, diet and lifestyle, and antioxidants.
What you getA plain-language on-screen report grouped by system, a PDF for your doctor, and automatic folic-acid flagging in your NuLevels Record stack when an MTHFR variant is found.
What it is notEducational, not a diagnosis. A genotype is a predisposition; the functional read is bloodwork. Confirm with your clinician before any change.
This tool reads about 30 well-studied, nutrition-relevant variants (including the MTHFR C677T / rs1801133 and A1298C / rs1801131 methylation variants) from a consumer DNA raw data file. Each is shown with your genotype and an educational, observational note; positions not present in your file are marked as not genotyped rather than guessed. It is educational and is not medical advice, a diagnosis, or a substitute for clinical genetic testing. A genotype indicates a predisposition, not a present deficiency; the functional readout is bloodwork such as homocysteine, active B12, and folate. Do not start, stop, or change any supplement or medication based on this report alone. Always confirm with your clinician.