What is CDKN2B-AS1 – rs10757274 and Why Does the Cardio Zoomer Test for It?

9p21 noncoding RNA variant
CDKN2B-AS1 – rs10757274 is a single-nucleotide variant in a long noncoding RNA at the 9p21 locus that influences nearby cell-cycle and vascular genes. Its presence is associated with inherited patterns of vascular biology; testing helps place genetic predisposition alongside blood and urine biomarkers for a clearer cardiovascular risk profile.
CDKN2B-AS1 – rs10757274
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About CDKN2B-AS1 – rs10757274
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CDKN2B-AS1 – rs10757274 FAQs

What is CDKN2B-AS1 – rs10757274 and why is it important?
It’s a common genetic variant in a long noncoding RNA region at 9p21 that affects regulation of nearby cell-cycle genes. Research shows the variant is associated with inherited differences in vascular biology and related risk patterns. Knowing this variant helps clinicians interpret why some cardiovascular markers or responses may differ between people.
What does it mean if my CDKN2B-AS1 – rs10757274 levels are low?
For a genetic test, “low” usually means you do not carry the risk-associated allele. That suggests this specific locus is less likely to be a strong inherited contributor to your vascular risk pattern, but other genetic variants, biomarkers, and lifestyle factors still matter. Your overall Cardio Zoomer results and clinical context determine how much weight to place on a non-risk genotype.
What does it mean if my CDKN2B-AS1 – rs10757274 levels are high?
“High” indicates presence of the allele that studies associate with a stronger inherited tendency toward certain vascular and cell-cycle patterns. This association can help explain why other biomarkers (inflammation, endothelial function, lipids) might behave differently, but interpretation requires the full panel and clinical context rather than relying on the SNP alone.
Why is this biomarker included in the Cardio Zoomer?
This SNP provides inherited context for vascular and cell-cycle biology that can interact with lipid, inflammatory, and endothelial markers. Including it helps clinicians integrate genetic predisposition with biochemical data to refine risk patterns and personalize monitoring and prevention strategies.

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