What is ACE – rs4343, rs4646994 and Why Does the Cardio Zoomer Test for It?

ACE gene functional variant
These common ACE gene variants (rs4343 and rs4646994) are linked to differences in angiotensin‑converting enzyme (ACE) activity. ACE helps control vascular tone and fluid balance by converting angiotensin I to angiotensin II and breaking down bradykinin, so genetic differences can help explain inherited patterns in angiotensin signaling and related cardiovascular biology.
ACE – rs4343, rs4646994
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About ACE – rs4343, rs4646994
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ACE – rs4343, rs4646994 FAQs

What is ACE – rs4343, rs4646994 and why is it important?
These are common genetic variants in the ACE gene that are linked to how much ACE enzyme a person tends to produce. ACE influences the balance of angiotensin II and bradykinin, which affect blood vessel tone and fluid handling. Knowing these variants provides context for inherited patterns in vascular and cardiometabolic biomarkers.
What does it mean if my ACE – rs4343, rs4646994 levels are low?
If your genotype is associated with lower ACE activity, it may be linked to relatively less angiotensin II formation and preserved bradykinin signaling. That pattern can align with different blood pressure and endothelial biomarker results than genotypes tied to higher ACE. Exact meaning depends on the rest of your Cardio Zoomer results and clinical context.
What does it mean if my ACE – rs4343, rs4646994 levels are high?
Genotypes associated with higher ACE activity tend to correspond with greater angiotensin II signaling and reduced bradykinin, which can relate to increased vascular tone and remodeling signals in other biomarkers. Elevated genetic propensity for ACE activity is an association, not a diagnosis, and should be interpreted together with blood markers, blood pressure data, and other genetic and clinical information.
Why is this biomarker included in the Cardio Zoomer?
These ACE variants offer inherited context for renin‑angiotensin system activity, helping clinicians link genetic tendency to observed biomarker patterns in blood pressure regulation, endothelial function, and inflammation. Including them supports a systems‑level readout that refines risk pattern interpretation and personalization of follow‑up testing and monitoring.

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