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Who was studied up to 820,192 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0113 lower (95% confidence interval 0.0083-0.0144); p = 6 × 10−13.
How common The G allele had a frequency of about 40% in the people studied.
Where it sits Chromosome 11, band 11p14.1 — between genes, 70 kb from LINC02758.
What each result means
A/ANo copy of the version the research linked to Smoking cessation (MTAG). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Smoking cessation (MTAG). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Smoking cessation (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2019 · PMID 30643251 · open access
Questions about rs59617050
What is rs59617050?
rs59617050 is a single position in the genome, in or near the near LINC02758 gene. Published research associates it with smoking cessation (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs59617050 linked to?
On MyGeneLog this position is linked to Smoking Behaviour and Nicotine Dependence. The research behind each link, and its sources, are set out on that condition page.
Does having rs59617050 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 rs59617050 come from?
GWAS Catalog, Nature genetics 2019, PMID:30643251. 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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