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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 8,894 European, Hispanic or African American individuals; replicated in up to 2,466 African American individuals, up to 15,619 European ancestry individuals, 1,734 Hispanic ancestry children.
The effect
Each copy of the G allele shifted the measure 0.441 higher (95% confidence interval 0.33-0.55); p = 2 × 10−14.
How common The G allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 16, band 16p11.2 — in an intron of SGF29.
What each result means
C/CNo copy of the version the research linked to Metabolite levels (methyl-4-hydroxybenzoate sulfate). This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Metabolite levels (methyl-4-hydroxybenzoate sulfate). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Metabolite levels (methyl-4-hydroxybenzoate sulfate). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2023 · PMID 37253714 · open access
Questions about rs9929532
What is rs9929532?
rs9929532 is a single position in the genome, in or near the SGF29 gene. Published research associates it with metabolite levels (methyl-4-hydroxybenzoate sulfate). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9929532 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 rs9929532 come from?
GWAS Catalog, Nature communications 2023, PMID:37253714. 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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