Gut microbiome abundance (class Bacteroides sp. 32) (at 3 months)
FOXP1 · rs62244881
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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 693 European ancestry, South Asian ancestry, East Asian ancestry, African American or Afro-Caribbean, Other admixed ancestry ancestry, Hispanic or Latin American, Greater Middle Eastern (Middle Eastern, North African or Persian), South East Asian ancestry, NR ancestry individuals.
The effect
Each copy of the C allele shifted the measure 1.44 higher (95% confidence interval 0.98-1.89); p = 9 × 10−10.
Where it sits Chromosome 3, band 3p13 — in an intron of FOXP1.
What each result means
C/CTwo copies of the version the research linked to Gut microbiome abundance (class Bacteroides sp. 32) (at 3 months). 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 Gut microbiome abundance (class Bacteroides sp. 32) (at 3 months). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Gut microbiome abundance (class Bacteroides sp. 32) (at 3 months). This is the starting point the study compared everyone against.
The Journal of allergy and clinical immunology · 2025 · PMID 40187613
Questions about rs62244881
What is rs62244881?
rs62244881 is a single position in the genome, in or near the FOXP1 gene. Published research associates it with gut microbiome abundance (class bacteroides sp. 32) (at 3 months). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62244881 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 rs62244881 come from?
GWAS Catalog, The Journal of allergy and clinical immunology 2025, PMID:40187613. 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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