What is COX-1 – rs1330344 and Why Does the Cardio Zoomer Test for It?

COX-1 gene variant
rs1330344 is a single‑letter genetic variant in the COX‑1 (PTGS1) gene, which helps make prostaglandins and thromboxane that affect platelet function and vascular tone. Testing this variant gives inherited context about prostaglandin/thromboxane pathways and how they may interact with other cardiovascular markers.
COX-1 – rs1330344
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About COX-1 – rs1330344
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COX-1 – rs1330344 FAQs

What is COX-1 – rs1330344 and why is it important?
rs1330344 is a common genetic variant in the COX‑1 (PTGS1) gene. COX‑1 helps produce prostaglandins and thromboxane, molecules that influence platelet activity and blood vessel function. Knowing this variant helps explain inherited differences in those pathways and complements blood-based measures in the Cardio Zoomer.
What does it mean if my COX-1 – rs1330344 levels are low?
For a genetic marker, “low” usually means you carry zero copies of the variant allele (reference genotype). That pattern aligns with the common COX‑1 sequence seen in many people and suggests no inherited change at this site. It doesn’t rule out altered platelet or vascular activity from other genes or non-genetic factors, so results are best interpreted with the full Cardio Zoomer profile.
What does it mean if my COX-1 – rs1330344 levels are high?
“High” indicates one or two copies of the rs1330344 variant allele. Studies have linked certain genotypes to modest shifts in COX‑1 expression or platelet-related signaling, which can be relevant to inflammation and clotting patterns. Any potential effect should be reviewed with other biomarkers and clinical information to determine its significance.
Why is this biomarker included in the Cardio Zoomer?
rs1330344 provides inherited insight into prostaglandin/thromboxane pathways and platelet biology, adding genetic context to the panel’s functional measures. Combined with lipids, inflammation, and clotting markers, it helps clinicians identify whether observed patterns reflect inherited tendencies or acquired changes, supporting more individualized interpretation.

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