Standard

Thyroid stimulating hormone levels

CD36 · rs10270183

What the study found

Who was studied 247,107 European ancestry individuals; replicated in 63,326 European ancestry individuals, 33,171 South Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0328 lower (95% confidence interval 0.025-0.041); p = 3 × 10−15.

How common The T allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 7, band 7q21.11 — in an intron of CD36.

What each result means

C/C No copy of the version the research linked to Thyroid stimulating hormone levels. This is the starting point the study compared everyone against.
C/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 rs10270183

What is rs10270183?

rs10270183 is a single position in the genome, in or near the CD36 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 rs10270183 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 rs10270183 come from?

GWAS Catalog, Nature communications 2023, PMID:37872160. 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 (rs10270183). MyGeneLog™. https://www.mygenelog.com/variants/rs10270183

← See all variants