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Who was studied 270,059 British ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.00949 lower (95% confidence interval 0.0065-0.0125); p = 4 × 10−10.
Where it sits Chromosome 3, band 3p12.1 — in an intron of CADM2.
What each result means
C/CNo copy of the version the research linked to Anxiety/tension (special factor of neuroticism). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Anxiety/tension (special factor of neuroticism). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Anxiety/tension (special 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 rs9828679
What is rs9828679?
rs9828679 is a single position in the genome, in or near the CADM2 gene. Published research associates it with anxiety/tension (special 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 rs9828679 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 rs9828679 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 rs9828679 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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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.
Anxiety/tension (special factor of neuroticism) (rs9828679). MyGeneLog™. https://www.mygenelog.com/variants/rs9828679