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Who was studied up to 146,117 European ancestry control.
The effect
Each copy of the C allele shifted the measure 0.0279 higher (95% confidence interval 0.02-0.036); p = 7 × 10−11.
How common The C allele had a frequency of about 68% in the people studied.
Where it sits Chromosome 20, band 20p12.1 — in an intron of MACROD2.
What each result means
C/CTwo copies of the version the research linked to Smoking behaviour (age at first cigarette). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Smoking behaviour (age at first cigarette). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Smoking behaviour (age at first cigarette). This is the starting point the study compared everyone against.
rs442467 is a single position in the genome, in or near the MACROD2 gene. Published research associates it with smoking behaviour (age at first cigarette). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs442467 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 rs442467 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 rs442467 come from?
GWAS Catalog, Biological psychiatry 2019, PMID:30679032. 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.
Smoking behaviour (age at first cigarette) (rs442467). MyGeneLog™. https://www.mygenelog.com/variants/rs442467