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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 9,869 European ancestry individuals, 1,363 African American individuals, 623 Chinese American individuals, 1,082 Hispanic American individuals; replicated in 12,177 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.11 lower (95% confidence interval 0.071-0.149); p = 3 × 10−10.
How common The T allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 11, band 11q24.2 — in an intron of ST3GAL4.
What each result means
C/CNo copy of the version the research linked to Soluble urokinase plasminogen activator receptor levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Soluble urokinase plasminogen activator receptor levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Soluble urokinase plasminogen activator receptor levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
The Journal of clinical investigation · 2022 · PMID 36194491 · open access
Questions about rs9704688
What is rs9704688?
rs9704688 is a single position in the genome, in or near the ST3GAL4 gene. Published research associates it with soluble urokinase plasminogen activator receptor levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9704688 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 rs9704688 come from?
GWAS Catalog, The Journal of clinical investigation 2022, PMID:36194491. 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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