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Neuroticism

SEMA6D · rs12442330

Where this position leads

Condition: Neuroticism

rs12442330 Condition: Neuroticism Neuroticism Condition rs12442330 rs12442330 SEMA6D

What the study found

Who was studied 449,484 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 6.38 z score higher (95% confidence interval -); p = 2 × 10−10.

Where it sits Chromosome 15, band 15q21.1 — in an intron of SEMA6D.

What each result means

C/C No copy of the version the research linked to Neuroticism. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Neuroticism. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Neuroticism. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs12442330

What is rs12442330?

rs12442330 is a single position in the genome, in or near the SEMA6D 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 rs12442330 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 rs12442330 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 rs12442330 come from?

GWAS Catalog, Nat Genet 2018, PMID:29942085. 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 (rs12442330). MyGeneLog™. https://www.mygenelog.com/variants/rs12442330

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