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Total testosterone levels

NOL4L-DT · rs11697333

What the study found

Who was studied 230,454 European ancestry women.

The effect Each copy of the T allele shifted the measure 0.0192 higher (95% confidence interval 0.013-0.025); p = 2 × 10−10.

How common The T allele had a frequency of about 67% in the people studied.

Where it sits Chromosome 20, band 20q11.21 — in an intron of NOL4L-DT.

What each result means

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

Questions about rs11697333

What is rs11697333?

rs11697333 is a single position in the genome, in or near the NOL4L-DT gene. Published research associates it with total 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 rs11697333 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 rs11697333 come from?

GWAS Catalog, Nature medicine 2020, PMID:32042192. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Total testosterone levels (rs11697333). MyGeneLog™. https://www.mygenelog.com/variants/rs11697333

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