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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 400 French ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.106 ug/mL higher (95% confidence interval 0.081-0.131); p = 1 × 10−12.
Where it sits Chromosome 13, band 13q14.13 — in an intron of CPB2-AS1.
What each result means
C/CTwo copies of the version the research linked to TAFI plasma levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to TAFI plasma levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to TAFI plasma levels. This is the starting point the study compared everyone against.
Genome medicine · 2022 · PMID 35264221 · open access
Questions about rs9534309
What is rs9534309?
rs9534309 is a single position in the genome, in or near the CPB2-AS1 gene. Published research associates it with tafi plasma levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9534309 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 rs9534309 come from?
GWAS Catalog, Genome medicine 2022, PMID:35264221. 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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