Gut microbiome abundance (class Bifidobacterium catenulatum) (at 3 months)
ARAP2 · rs10029045
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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 up to 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, unknown ancestry males.
The effect
Each copy of the T allele shifted the measure 1.05 lower (95% confidence interval -1.41--0.69); p = 2 × 10−8.
Where it sits Chromosome 4, band 4p14 — inside ARAP2.
What each result means
A/ANo copy of the version the research linked to Gut microbiome abundance (class Bifidobacterium catenulatum) (at 3 months). This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to Gut microbiome abundance (class Bifidobacterium catenulatum) (at 3 months). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Gut microbiome abundance (class Bifidobacterium catenulatum) (at 3 months). That is the strongest link of the three results. A link in a study is not a diagnosis.
The Journal of allergy and clinical immunology · 2025 · PMID 40187613
Questions about rs10029045
What is rs10029045?
rs10029045 is a single position in the genome, in or near the ARAP2 gene. Published research associates it with gut microbiome abundance (class bifidobacterium catenulatum) (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 rs10029045 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 rs10029045 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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