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Total testosterone levels

NR2F6 · rs202200760

What the study found

Who was studied 194,453 European ancestry men.

The effect Each copy of the C allele shifted the measure 0.12 higher (95% confidence interval 0.1-0.14); p = 9 × 10−48.

How common The C allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 19, band 19p13.11 — a missense change in NR2F6.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Total testosterone levels compared to the general population.
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Total testosterone levels.
G/G Published research associates this genotype with typical/baseline likelihood of Total testosterone levels — no copies of the reported risk allele.
Source

Questions about rs202200760

What is rs202200760?

rs202200760 is a single position in the genome, in or near the NR2F6 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 rs202200760 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 rs202200760 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 (rs202200760). MyGeneLog™. https://www.mygenelog.com/variants/rs202200760

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