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Hypothyroidism

near P2RY10 · rs57033802

Where this position leads

Condition: Hypothyroidism

rs57033802 Condition: Hypothyroidism Hypothyroidism Condition rs57033802 rs57033802 near P2RY10

What the study found

Who was studied 30,155 European ancestry cases, 379,986 European ancestry controls, 1,114 East Asian ancestry cases, 172,656 East Asian ancestry controls.

The effect Each copy of the T allele shifted the measure 0.13 lower (95% confidence interval 0.095-0.164); p = 1 × 10−13.

Where it sits Chromosome X, band Xq21.1 — between genes, 9.8 kb from P2RY10.

What each result means

C/C No copy of the version the research linked to Hypothyroidism. This is the starting point the study compared everyone against.
C/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 rs57033802

What is rs57033802?

rs57033802 is a single position in the genome, in or near the near P2RY10 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 rs57033802 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 rs57033802 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 rs57033802 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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 (rs57033802). MyGeneLog™. https://www.mygenelog.com/variants/rs57033802

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