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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 2,935 Qatari ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.479 higher (95% confidence interval 0.41-0.55); p = 3 × 10−37.
How common The A allele had a frequency of about 15% in the people studied.
Where it sits Chromosome 17, band 17q11.2 — between genes, 12.4 kb from LINC01992.
What each result means
A/ATwo copies of the version the research linked to Vitronectin 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 Vitronectin levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Vitronectin levels. This is the starting point the study compared everyone against.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs4497747
What is rs4497747?
rs4497747 is a single position in the genome, in or near the near LINC01992 gene. Published research associates it with vitronectin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4497747 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 rs4497747 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. 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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