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Who was studied 270,059 British ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0112 higher (95% confidence interval 0.0078-0.0146); p = 9 × 10−11.
Where it sits Chromosome 8, band 8p23.1 — in an intron of FAM167A.
What each result means
A/ANo copy of the version the research linked to General factor of neuroticism. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to General factor of neuroticism. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to General factor of neuroticism. That is the strongest link of the three results. A link in a study is not a diagnosis.
Molecular psychiatry · 2020 · PMID 30867560 · open access
Questions about rs2736318
What is rs2736318?
rs2736318 is a single position in the genome, in or near the FAM167A gene. Published research associates it with general factor of 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 rs2736318 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 rs2736318 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 rs2736318 come from?
GWAS Catalog, Molecular psychiatry 2020, PMID:30867560. 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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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.
General factor of neuroticism (rs2736318). MyGeneLog™. https://www.mygenelog.com/variants/rs2736318