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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 5,284 Finnish ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.51 higher; p = 3 × 10−14.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 12, band 12q23.3 — in an intron of GLT8D2.
What each result means
A/ATwo copies of the version the research linked to Soluble VCAM-1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Soluble VCAM-1 levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Soluble VCAM-1 levels. This is the starting point the study compared everyone against.
Journal of medical genetics · 2019 · PMID 31217265 · open access
Questions about rs117238625
What is rs117238625?
rs117238625 is a single position in the genome, in or near the HSP90B1 gene. Published research associates it with soluble vcam-1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117238625 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 rs117238625 come from?
GWAS Catalog, Journal of medical genetics 2019, PMID:31217265. 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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