Standard

Smoking initiation (ever regular vs never regular) (MTAG)

near RNU6-679P · rs10073418

Where this position leads

Condition: Smoking Behaviour and Nicotine Dependence

rs10073418 Condition: Smoking Behaviour and Nicotine Dependence Smoking Behaviour and Nicotine Dependence Condition rs10073418 rs10073418 near RNU6-67…

What the study found

Who was studied up to 1,359,002 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0072 higher (95% confidence interval 0.005-0.0094); p = 2 × 10−10.

How common The A allele had a frequency of about 34% in the people studied.

Where it sits Chromosome 5, band 5p15.2 — between genes, 32.7 kb from RNU6-679P.

What each result means

A/A Two copies of the version the research linked to Smoking initiation (ever regular vs never regular) (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Smoking initiation (ever regular vs never regular) (MTAG). That is a smaller link than two copies.
G/G No copy of the version the research linked to Smoking initiation (ever regular vs never regular) (MTAG). This is the starting point the study compared everyone against.
Source

Questions about rs10073418

What is rs10073418?

rs10073418 is a single position in the genome, in or near the near RNU6-679P gene. Published research associates it with smoking initiation (ever regular vs never regular) (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 rs10073418 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 rs10073418 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 rs10073418 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.

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 initiation (ever regular vs never regular) (MTAG) (rs10073418). MyGeneLog™. https://www.mygenelog.com/variants/rs10073418

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