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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 14,735 European ancestry individuals; replicated in 1,585 European or unknown ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.116 higher (95% confidence interval 0.091-0.141); p = 8 × 10−19.
How common The C allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 2, band 2q32.2 — in an intron of SLC40A1.
What each result means
C/CTwo copies of the version the research linked to Fibroblast growth factor 23 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 Fibroblast growth factor 23 levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Fibroblast growth factor 23 levels. This is the starting point the study compared everyone against.
Nature immunology · 2023 · PMID 37563310 · open access
Questions about rs3811621
What is rs3811621?
rs3811621 is a single position in the genome, in or near the SLC40A1 gene. Published research associates it with fibroblast growth factor 23 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs3811621 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 rs3811621 come from?
GWAS Catalog, Nature immunology 2023, PMID:37563310. 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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