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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 6,136 Finnish ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.58 higher.
Where it sits Chromosome X, band Xq28 — in an intron of VBP1.
What each result means
A/ANo copy of the version the research linked to X-23666 levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to X-23666 levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to X-23666 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2022 · PMID 35347128 · open access
Questions about rs35296872
What is rs35296872?
rs35296872 is a single position in the genome, in or near the VBP1 gene. Published research associates it with x-23666 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs35296872 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 rs35296872 come from?
GWAS Catalog, Nature communications 2022, PMID:35347128. 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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