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Hypothyroidism

ARMC2 · rs12193858

Where this position leads

Condition: Hypothyroidism

rs12193858 Condition: Hypothyroidism Hypothyroidism Condition rs12193858 rs12193858 ARMC2

What the study found

Who was studied 58,783 European ancestry cases, 633,203 European ancestry controls.

The effect Each copy of the T allele carried 1.08 times the odds of Hypothyroidism (95% confidence interval 1.05-1.1); p = 1 × 10−10.

Where it sits Chromosome 6, band 6q21 — in an intron of ARMC2.

What each result means

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

Questions about rs12193858

What is rs12193858?

rs12193858 is a single position in the genome, in or near the ARMC2 gene. Published research associates it with hypothyroidism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs12193858 linked to?

On MyGeneLog this position is linked to Hypothyroidism. The research behind each link, and its sources, are set out on that condition page.

Does having rs12193858 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 rs12193858 come from?

GWAS Catalog, European journal of endocrinology 2024, PMID:39067062. 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.

Hypothyroidism (rs12193858). MyGeneLog™. https://www.mygenelog.com/variants/rs12193858

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