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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 2,083,151 European ancestry individuals; replicated in 287,239 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0131 lower (95% confidence interval 0.0088-0.0174); p = 2 × 10−9.
How common The A allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 1, band 1p31.1 — between genes, 0.3 kb from LHX8.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Well-being spectrum (multivariate analysis) compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Well-being spectrum (multivariate analysis).
G/GPublished research associates this genotype with typical/baseline likelihood of Well-being spectrum (multivariate analysis) — no copies of the reported risk allele.
rs17622606 is a single position in the genome, in or near the near LHX8 gene. Published research associates it with well-being spectrum (multivariate analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17622606 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 rs17622606 come from?
GWAS Catalog, Nat Genet 2019, PMID:30643256. 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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