What is LPL – rs328, rs7007797, rs264, rs320 and Why Does the Cardio Zoomer Test for It?

Lipoprotein lipase gene variants
These are common genetic variants in the LPL gene, which encodes lipoprotein lipase, an enzyme that helps clear triglyceride-rich particles from blood. Testing these variants gives inherited context for how an individual’s body processes fats and can help explain differences in lipid patterns when viewed with other Cardio Zoomer markers.
LPL – rs328, rs7007797, rs264, rs320
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About LPL – rs328, rs7007797, rs264, rs320
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LPL – rs328, rs7007797, rs264, rs320 FAQs

What is LPL – rs328, rs7007797, rs264, rs320 and why is it important?
These are common genetic variants in the LPL gene, which influences how the body breaks down triglyceride-rich particles. They matter because they help explain inherited tendencies in triglyceride levels and lipid patterns. That genetic context can clarify why two people with similar cholesterol numbers may have different underlying biology.
What does it mean if my LPL – rs328, rs7007797, rs264, rs320 levels are low?
Genetic reports don’t give “levels,” but some variant combinations are linked with lower predicted LPL activity. Those associations generally align with slower triglyceride clearance and higher triglyceride-rich particles in blood. Clinical meaning depends on the full Cardio Zoomer profile and other metabolic or lifestyle factors.
What does it mean if my LPL – rs328, rs7007797, rs264, rs320 levels are high?
Some LPL variants are associated with higher predicted enzyme activity, which tends to align with lower fasting triglycerides and different HDL patterns. Elevated predicted activity is an association, not a standalone outcome; interpretation requires integrating genetic results with lipid measures and other Cardio Zoomer markers.
Why is this biomarker included in the Cardio Zoomer?
LPL variants add inherited information about triglyceride clearance and lipid particle behavior. Paired with advanced lipid, inflammatory, and metabolic markers in Cardio Zoomer, they help providers distinguish genetic contributors from modifiable drivers and refine personalized risk assessment.

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