Standard

Total testosterone levels

MAP2K7 · rs8107967

What the study found

Who was studied 194,453 European ancestry men.

The effect Each copy of the G allele shifted the measure 0.0187 higher (95% confidence interval 0.013-0.025); p = 2 × 10−10.

How common The G allele had a frequency of about 57% in the people studied.

Where it sits Chromosome 19, band 19p13.2 — in an intron of MAP2K7.

What each result means

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

Questions about rs8107967

What is rs8107967?

rs8107967 is a single position in the genome, in or near the MAP2K7 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 rs8107967 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 rs8107967 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

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.

Total testosterone levels (rs8107967). MyGeneLog™. https://www.mygenelog.com/variants/rs8107967

← See all variants