Standard

Hypothyroidism

near IL2RA · rs7072793

Where this position leads

Condition: Hypothyroidism

rs7072793 Condition: Hypothyroidism Hypothyroidism Condition rs7072793 rs7072793 near IL2RA

What the study found

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

The effect Each copy of the C allele carried 1.08 times the odds of Hypothyroidism (95% confidence interval 1.07-1.1); p = 8 × 10−23.

Where it sits Chromosome 10, band 10p15.1 — between genes, 1.9 kb from IL2RA.

What each result means

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

Questions about rs7072793

What is rs7072793?

rs7072793 is a single position in the genome, in or near the near IL2RA 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 rs7072793 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 rs7072793 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 rs7072793 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 (rs7072793). MyGeneLog™. https://www.mygenelog.com/variants/rs7072793

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