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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 1,400,535 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0102 lower (95% confidence interval 0.0071-0.0133); p = 2 × 10−10.
How common The G allele had a frequency of about 19% in the people studied.
Where it sits Chromosome 10, band 10q23.1 — between genes, 55.6 kb from LINC02647.
What each result means
A/ANo copy of the version the research linked to Smoking cessation. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Smoking cessation. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Smoking cessation. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs11201563 is a single position in the genome, in or near the near LINC02647 gene. Published research associates it with smoking cessation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11201563 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 rs11201563 come from?
GWAS Catalog, Nature 2022, PMID:36477530. 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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