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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 45,330 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.407 higher (95% confidence interval 0.32-0.5); p = 2 × 10−18.
How common The C allele had a frequency of about 99% in the people studied.
Where it sits Chromosome 11, band 11q23.3 — in an intron of PAFAH1B2.
What each result means
C/CTwo copies of the version the research linked to Soluble transferrin receptor concentration. 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 Soluble transferrin receptor concentration. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Soluble transferrin receptor concentration. This is the starting point the study compared everyone against.
Communications biology · 2024 · PMID 39643614 · open access
Questions about rs187669805
What is rs187669805?
rs187669805 is a single position in the genome, in or near the PAFAH1B2 gene. Published research associates it with soluble transferrin receptor concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs187669805 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 rs187669805 come from?
GWAS Catalog, Communications biology 2024, PMID:39643614. 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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