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Regular attendance at a pub or social club

LOC100130899 · rs139920

What the study found

Who was studied 124,047 European ancestry cases, 328,255 European ancestry controls.

The effect Each copy of the C allele shifted the measure 0.00581 lower (95% confidence interval 0.004-0.0076); p = 3 × 10−10.

How common The C allele had a frequency of about 49% in the people studied.

Where it sits Chromosome 22, band 22q13.1 — in the 3′ untranslated region of TNRC6B.

What each result means

C/C Two copies of the version the research linked to Regular attendance at a pub or social club. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Regular attendance at a pub or social club. That is a smaller link than two copies.
T/T No copy of the version the research linked to Regular attendance at a pub or social club. This is the starting point the study compared everyone against.
Source

Questions about rs139920

What is rs139920?

rs139920 is a single position in the genome, in or near the LOC100130899 gene. Published research associates it with regular attendance at a pub or social club. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs139920 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 rs139920 come from?

GWAS Catalog, Nat Commun 2018, PMID:29970889. 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.

Regular attendance at a pub or social club (rs139920). MyGeneLog™. https://www.mygenelog.com/variants/rs139920

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