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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 13,781 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 6.79 mg/dL higher (95% confidence interval 4.46-9.12); p = 5 × 10−11.
Where it sits Chromosome 6, band 6q26 — between genes, 46.3 kb from PLG.
What each result means
C/CTwo copies of the version the research linked to Lipoprotein (a) 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 Lipoprotein (a) levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Lipoprotein (a) levels. This is the starting point the study compared everyone against.
Journal of lipid research · 2017 · PMID 28512139 · open access
Questions about rs139699952
What is rs139699952?
rs139699952 is a single position in the genome, in or near the LPA gene. Published research associates it with lipoprotein (a) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs139699952 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 rs139699952 come from?
GWAS Catalog, Journal of lipid research 2017, PMID:28512139. 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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