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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 982 Scottish ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.358 lower (95% confidence interval 0.25-0.47); p = 2 × 10−10.
How common The C allele had a frequency of about 20% in the people studied.
Where it sits Chromosome 1, band 1q23.2 — between genes, 6.2 kb from OR10J3.
What each result means
C/CTwo copies of the version the research linked to Monocyte chemoattractant protein-4 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Monocyte chemoattractant protein-4 levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Monocyte chemoattractant protein-4 levels. This is the starting point the study compared everyone against.
Genome medicine · 2020 · PMID 32641083 · open access
Questions about rs4269772
What is rs4269772?
rs4269772 is a single position in the genome, in or near the near OR10J3 gene. Published research associates it with monocyte chemoattractant protein-4 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4269772 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 rs4269772 come from?
GWAS Catalog, Genome medicine 2020, PMID:32641083. 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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