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Special factor anxiety/tension in mitochondrial haplogroup T

near LINC01613 · rs181210427

What the study found

Who was studied 26,893 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.152 lower (95% confidence interval 0.1-0.2); p = 3 × 10−9.

Where it sits Chromosome 9, band 9q33.1 — between genes, 211.8 kb from LINC01613.

What each result means

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

Questions about rs181210427

What is rs181210427?

rs181210427 is a single position in the genome, in or near the near LINC01613 gene. Published research associates it with special factor anxiety/tension in mitochondrial haplogroup t. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs181210427 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 rs181210427 come from?

GWAS Catalog, Nature communications 2023, PMID:37253732. 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.

Special factor anxiety/tension in mitochondrial haplogroup T (rs181210427). MyGeneLog™. https://www.mygenelog.com/variants/rs181210427

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