Who was studied up to 357,854 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0327 lower (95% confidence interval 0.022-0.044); p = 4 × 10−9.
How common The T allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 16, band 16p12.1 — in an intron of TNRC6A.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Alcohol consumption (drinks per week) — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Alcohol consumption (drinks per week).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Alcohol consumption (drinks per week) compared to the general population.
rs17177078 is a single position in the genome, in or near the TNRC6A gene. Published research associates it with alcohol consumption (drinks per week). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17177078 linked to?
On MyGeneLog this position is linked to Alcohol Consumption. The research behind each link, and its sources, are set out on that condition page.
Does having rs17177078 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 rs17177078 come from?
GWAS Catalog, Biol Psychiatry 2018, 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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Alcohol consumption (drinks per week) (rs17177078). MyGeneLog™. https://www.mygenelog.com/variants/rs17177078