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Who was studied up to 931,815 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0117 higher (95% confidence interval 0.0079-0.0154); p = 1 × 10−9.
How common The C allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 5, band 5p12 — in an intron of HCN1.
What each result means
A/ANo copy of the version the research linked to Age of smoking initiation (MTAG). This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Age of smoking initiation (MTAG). That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Age of smoking initiation (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 rs62367520
What is rs62367520?
rs62367520 is a single position in the genome, in or near the HCN1 gene. Published research associates it with age of smoking initiation (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 rs62367520 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 rs62367520 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 rs62367520 come from?
GWAS Catalog, Nat Genet 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Age of smoking initiation (MTAG) (rs62367520). MyGeneLog™. https://www.mygenelog.com/variants/rs62367520