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General factor of neuroticism

ENSG00000239065 · rs12680442

Where this position leads

Condition: Neuroticism

rs12680442 Condition: Neuroticism Neuroticism Condition rs12680442 rs12680442 ENSG00000239…

What the study found

Who was studied 270,059 British ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.00997 lower (95% confidence interval 0.0066-0.0133); p = 6 × 10−9.

Where it sits Chromosome 8, band 8p23.1 — between genes, 34.3 kb from MIR124-1HG.

What each result means

C/C Two 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.
C/T One copy of the version the research linked to General factor of neuroticism. That is a smaller link than two copies.
T/T No copy of the version the research linked to General factor of neuroticism. This is the starting point the study compared everyone against.
Source

Questions about rs12680442

What is rs12680442?

rs12680442 is a single position in the genome, in or near the ENSG00000239065 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 rs12680442 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 rs12680442 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 rs12680442 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.

Quoting this page

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General factor of neuroticism (rs12680442). MyGeneLog™. https://www.mygenelog.com/variants/rs12680442

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