What is CYP1A2 (rs762551)? And Why Does the Toxin Zoomer Test for It?

Phase I xenobiotic enzyme variant
CYP1A2 (rs762551) is a common genetic variant in the CYP1A2 gene that influences activity of a phase I liver enzyme. That enzyme helps chemically modify many environmental chemicals and some drugs, so genotypes can hint at individual differences in how the body processes toxicants. Measuring this variant adds genetic context when interpreting toxicant levels and detox capacity.
CYP1A2 (rs762551)
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About CYP1A2 (rs762551)
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CYP1A2 (rs762551) FAQs

What is CYP1A2 (rs762551) and why is it important?
rs762551 is a single-letter genetic change in the CYP1A2 gene that is linked to differences in enzyme activity. That enzyme performs early chemical changes on many environmental compounds and some drugs. Knowing this variant helps explain why two people with similar exposures can have different measured toxicant patterns or sensitivity.
What does it mean if my CYP1A2 (rs762551) levels are low?
A low or reduced predicted CYP1A2 activity suggests slower phase I processing for substrates of this enzyme. That can be associated with longer presence of some parent compounds in the body and different patterns of metabolites. Clinical interpretation requires comparing this result with urinary toxicant levels and other genetic markers on the full panel.
What does it mean if my CYP1A2 (rs762551) levels are high?
Higher predicted CYP1A2 activity suggests faster initial conversion of certain chemicals and compounds. That may shorten exposure to some parent toxins but can sometimes increase temporary formation of reactive intermediates. These implications depend on the specific toxicants measured and other detoxification pathways, so context from the full report matters.
Why is this biomarker included in the Toxin Zoomer?
CYP1A2 rs762551 helps map an individual’s phase I metabolic tendency, which affects how environmental chemicals are transformed. When combined with measured toxicant loads and other detox genes, it improves interpretation of exposure patterns and supports more personalized clinical assessment.

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