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Thyroid stimulating hormone levels

near ATP5F1CP1 · rs10873079

What the study found

Who was studied 482,873 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.018 higher (95% confidence interval 0.014-0.022); p = 9 × 10−13.

How common The T allele had a frequency of about 75% in the people studied.

Where it sits Chromosome 14, band 14q22.2 — between genes, 144.8 kb from ATP5F1CP1.

What each result means

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

Questions about rs10873079

What is rs10873079?

rs10873079 is a single position in the genome, in or near the near ATP5F1CP1 gene. Published research associates it with thyroid stimulating hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10873079 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 rs10873079 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.

Thyroid stimulating hormone levels (rs10873079). MyGeneLog™. https://www.mygenelog.com/variants/rs10873079

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