What is PHACTR1 – rs12526453, rs169713 and Why Does the Cardio Zoomer Test for It?

Vascular-regulating gene variants
These are common single‑nucleotide variants in the PHACTR1 gene that influence how vascular cells organize their cytoskeleton and respond to mechanical or biochemical signals. Knowing a person’s PHACTR1 genotype provides inherited context that helps interpret patterns in vascular function and cardiovascular trait profiles when combined with other biomarkers.
PHACTR1 – rs12526453, rs169713
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About PHACTR1 – rs12526453, rs169713
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PHACTR1 – rs12526453, rs169713 FAQs

What is PHACTR1 – rs12526453, rs169713 and why is it important?
These are common genetic variants in the PHACTR1 gene, which helps regulate cell shape and movement in blood‑vessel walls. Research shows certain alleles are associated with different patterns of vascular structure and response. That information adds inherited context to other cardiovascular test results and helps clinicians interpret overall vascular biology.
What does it mean if my PHACTR1 – rs12526453, rs169713 levels are low?
For SNPs, “low” typically means you do not carry the allele linked to the studied association. That pattern is associated at the population level with a different vascular‑biology profile than carriers. It does not by itself predict outcomes; results are most informative when combined with other Cardio Zoomer biomarkers and clinical information.
What does it mean if my PHACTR1 – rs12526453, rs169713 levels are high?
If you carry the allele that has been linked in studies to PHACTR1‑related effects, that association indicates a population‑level tendency toward certain vascular patterns (for example, differences in vessel wall behavior). Elevated carriage is an inherited risk pattern, not a diagnosis, and must be interpreted alongside other laboratory, imaging, and clinical data.
Why is this biomarker included in the Cardio Zoomer?
PHACTR1 SNPs provide genetic insight into vascular cell behavior that complements biochemical markers of lipids, inflammation, and endothelial function. Including these variants helps providers distinguish inherited contributors from acquired changes and supports more precise, personalized interpretation of the overall cardiovascular profile.

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