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Total testosterone levels

near ETS1 · rs76299412

What the study found

Who was studied 230,454 European ancestry women.

The effect Each copy of the A allele shifted the measure 0.0349 higher (95% confidence interval 0.027-0.043); p = 2 × 10−20.

How common The A allele had a frequency of about 15% in the people studied.

Where it sits Chromosome 11, band 11q24.3 — between genes, 59.6 kb from ETS1.

What each result means

A/A 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.
A/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 rs76299412

What is rs76299412?

rs76299412 is a single position in the genome, in or near the near ETS1 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 rs76299412 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 rs76299412 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 (rs76299412). MyGeneLog™. https://www.mygenelog.com/variants/rs76299412

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