What is KIF6 – rs20455 and Why Does the Cardio Zoomer Test for It?

Kinesin motor protein variant
KIF6 – rs20455 is a common single-nucleotide variant in the KIF6 gene that changes one amino acid in a kinesin motor protein. Kinesins help move cargo along microtubules inside cells, and this variant has been studied for its associations with cardiovascular traits and medication-response patterns. Testing the variant adds inherited-pattern information that complements blood and urine markers in Cardio Zoomer.
KIF6 – rs20455
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About KIF6 – rs20455
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KIF6 – rs20455 FAQs

What is KIF6 – rs20455 and why is it important?
KIF6 – rs20455 is a single-letter genetic change in the KIF6 gene that alters a kinesin motor protein. Researchers have studied it for links to cardiovascular-related traits and differences in medication response. Knowing a person’s rs20455 genotype adds inherited-context information that can help interpret other Cardio Zoomer results.
What does it mean if my KIF6 – rs20455 levels are low?
Genetic testing reports genotype rather than ‘‘levels,’’ so ‘‘low’’ typically means zero copies of the variant allele. Fewer or no copies of the 719R allele means the specific associations seen in some studies are less likely to apply to you. This information is most useful when combined with the rest of your Cardio Zoomer biomarkers and clinical context.
What does it mean if my KIF6 – rs20455 levels are high?
‘‘High’’ in a genetic sense usually means one or two copies of the variant allele are present. Some studies have observed modest associations between having the variant and certain cardiovascular-related patterns or medication responses, but findings are inconsistent. Any potential implications should be interpreted alongside your full Cardio Zoomer profile and clinical assessment.
Why is KIF6 – rs20455 included in the Cardio Zoomer?
Including rs20455 provides inherited-pattern information that complements biochemical markers of lipids, inflammation, metabolism, and vascular function. It helps clinicians see whether genetic tendencies align with or contradict other test signals, improving the precision of risk-pattern interpretation. The variant contributes to a more complete, personalized cardiovascular assessment without replacing other biomarkers.

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