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Neuroticism

near MSRA · rs7813389

Where this position leads

What the study found

Who was studied 523,783 European ancestry individuals; replicated in 59,206 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.011 lower (95% confidence interval 0.0073-0.0146); p = 5 × 10⁻⁹.

How common The T allele had a frequency of about 40% in the people studied.

Where it sits Chromosome 8, band 8p23.1 — in an intron of MSRA-DT.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Neuroticism — no copies of the reported risk allele.

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Neuroticism.

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Neuroticism compared to the general population.

Source

Multivariate genome-wide analyses of the well-being spectrum

Baselmans BML, Jansen R, Ip HF, van Dongen J, Abdellaoui A, van de Weijer MP, Bao Y, Smart M, Kumari M, Willemsen G, Hottenga JJ, Boomsma DI

and 3 more — show all

de Geus EJC, Nivard MG, Bartels M

BIOS consortium · Social Science Genetic Association Consortium

Nature genetics · 2019 · PMID 30643256

Questions about rs7813389

What is rs7813389?

rs7813389 is a single position in the genome, in or near the near MSRA gene. Published research associates it with neuroticism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7813389 linked to?

On MyGeneLog this position is linked to Neuroticism. The research behind each link, and its sources, are set out on that condition page.

Does having rs7813389 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 rs7813389 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.

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.

Neuroticism (rs7813389). MyGeneLog™. https://www.mygenelog.com/variants/rs7813389

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