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Free testosterone levels

near LINC01515 · rs10400066

What the study found

Who was studied 148,248 British ancestry men.

The effect Each copy of the C allele shifted the measure 0 nmol/L higher (95% confidence interval 0-0); p = 6 × 10−37.

How common The C allele had a frequency of about 40% in the people studied.

Where it sits Chromosome 10, band 10q21.3 — between genes, 27.2 kb from LINC01515.

What each result means

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

Questions about rs10400066

What is rs10400066?

rs10400066 is a single position in the genome, in or near the near LINC01515 gene. Published research associates it with free testosterone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10400066 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 rs10400066 come from?

GWAS Catalog, Science advances 2021, PMID:34321204. 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.

Free testosterone levels (rs10400066). MyGeneLog™. https://www.mygenelog.com/variants/rs10400066

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