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Who was studied 388,538 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0119 higher (95% confidence interval 0.0078-0.016); p = 6 × 10−9.
How common The T allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 5, band 5q11.1 — between genes, 47.6 kb from RNU6-1296P.
What each result means
C/CNo copy of the version the research linked to Subjective well-being (MTAG). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Subjective well-being (MTAG). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Subjective well-being (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2018 · PMID 29292387 · open access
Questions about rs17820772
What is rs17820772?
rs17820772 is a single position in the genome, in or near the near RNU6-1296P gene. Published research associates it with subjective well-being (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 rs17820772 linked to?
On MyGeneLog this position is linked to Depression (Self-Reported Symptoms). The research behind each link, and its sources, are set out on that condition page.
Does having rs17820772 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 rs17820772 come from?
GWAS Catalog, Nature genetics 2018, PMID:29292387. 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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