What is ALDH2 – rs671 and Why Does the Cardio Zoomer Test for It?

Mitochondrial aldehyde-metabolism variant
ALDH2 – rs671 is a common genetic variant that changes activity of the mitochondrial aldehyde dehydrogenase enzyme, which clears reactive aldehydes from metabolism. Testing this variant helps reveal inherited differences in aldehyde clearance, oxidative stress burden, and drug-response patterns relevant to cardiovascular biology.
ALDH2 – rs671
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About ALDH2 – rs671
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ALDH2 – rs671 FAQs

What is ALDH2 – rs671 and why is it important?
ALDH2 – rs671 is a genetic change that affects how well the mitochondrial ALDH2 enzyme clears reactive aldehydes. Those aldehydes come from alcohol metabolism and from oxidative damage to fats and proteins. The variant matters because altered aldehyde handling can influence oxidative stress signals, vascular biology, and how some medications are processed.
What does it mean if my ALDH2 – rs671 levels are low?
When people say ALDH2 activity is low, they’re referring to a genotype that reduces enzyme function (the rs671 variant). That profile is associated with slower aldehyde clearance and higher aldehyde exposure, which tends to show up as changes in oxidative stress and related vascular markers. Interpretation depends on other lab results and clinical factors rather than the genotype alone.
What does it mean if my ALDH2 – rs671 levels are high?
Higher ALDH2 activity generally reflects the wild-type genotype and more efficient aldehyde detoxification. That pattern is associated with lower aldehyde-related stress signals and different expected responses on oxidative and endothelial biomarkers. Clinical meaning is determined by combining this genetic result with the rest of the Cardio Zoomer data and patient context.
Why is ALDH2 – rs671 included in the Cardio Zoomer?
Including ALDH2 – rs671 helps explain inherited differences in aldehyde metabolism that can shape oxidative stress, endothelial function, and drug response patterns. This genetic context improves interpretation of redox and vascular markers and supports more precise, personalized assessment of cardiovascular-related biology.

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