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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 4,291 European ancestry men, 3,352 European ancestry women.
The effect
Each copy of the C allele shifted the measure 0.231 lower (95% confidence interval 0.15-0.31); p = 1 × 10−8.
How common The C allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 17, band 17p13.1 — in an intron of ZBTB4.
What each result means
C/CTwo copies of the version the research linked to Testosterone levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Testosterone levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Testosterone levels. This is the starting point the study compared everyone against.
The Journal of clinical endocrinology and metabolism · 2019 · PMID 31169883
Questions about rs3867595
What is rs3867595?
rs3867595 is a single position in the genome, in or near the ZBTB4 gene. Published research associates it with 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 rs3867595 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 rs3867595 come from?
GWAS Catalog, The Journal of clinical endocrinology and metabolism 2019, PMID:31169883. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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