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Hypothyroidism

MACIR · rs2288786

Where this position leads

Conditions: Hypothyroidism, Thyroid Stimulating Hormone (TSH) Levels

rs2288786 Condition: Hypothyroidism Hypothyroidism Condition Condition: Thyroid Stimulating Hormone (TSH) Levels Thyroid Stimulating Hormone (TSH) Levels Condition rs2288786 rs2288786 MACIR

What the study found

Who was studied 98,805 European ancestry cases, 948,186 European ancestry controls, 14,588 cases, 117,082 controls; replicated in 34,835 European ancestry cases, 492,149 European ancestry controls.

The effect Each copy of the A allele shifted the measure 0.061 lower (95% confidence interval 0.051-0.071); p = 1 × 10−31.

How common The A allele had a frequency of about 32% in the people studied.

Where it sits Chromosome 5, band 5q21.1 — in an intron of MACIR.

What each result means

A/A 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.
A/G One copy of the version the research linked to Hypothyroidism. That is a smaller link than two copies.
G/G No copy of the version the research linked to Hypothyroidism. This is the starting point the study compared everyone against.
Source

Questions about rs2288786

What is rs2288786?

rs2288786 is a single position in the genome, in or near the MACIR 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 rs2288786 linked to?

On MyGeneLog this position is linked to Hypothyroidism, Thyroid Stimulating Hormone (TSH) Levels. The research behind each link, and its sources, are set out on that condition page.

Does having rs2288786 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 rs2288786 come from?

GWAS Catalog, Nature genetics 2025, PMID:41238958. 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 (rs2288786). MyGeneLog™. https://www.mygenelog.com/variants/rs2288786

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