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Who was studied 71,019 Korean ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.055 lower (95% confidence interval 0.036-0.074); p = 1 × 10−8.
How common The T allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 12, band 12q24.31 — in an intron of CABP1.
What each result means
C/CNo copy of the version the research linked to High-sensitivity C-reactive protein levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to High-sensitivity C-reactive protein levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to High-sensitivity C-reactive protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Scientific reports · 2025 · PMID 39747571 · open access
Questions about rs7965649
What is rs7965649?
rs7965649 is a single position in the genome, in or near the CABP1 gene. Published research associates it with high-sensitivity c-reactive protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7965649 linked to?
On MyGeneLog this position is linked to C-Reactive Protein Levels. The research behind each link, and its sources, are set out on that condition page.
Does having rs7965649 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs7965649 come from?
GWAS Catalog, Scientific reports 2025, PMID:39747571. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Quoting this page
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High-sensitivity C-reactive protein levels (rs7965649). MyGeneLog™. https://www.mygenelog.com/variants/rs7965649