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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 8,938 European ancestry male individuals; replicated in 5,491 European ancestry male individuals.
The effect
Each copy of the T allele shifted the measure 31.8 ng/dl higher (95% confidence interval 27.29-36.31); p = 1 × 10−41.
How common The T allele had a frequency of about 23% in the people studied.
Where it sits Chromosome 17, band 17p13.1 — in an intron of SHBG.
What each result means
G/GNo copy of the version the research linked to Testosterone levels. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Testosterone levels. That is a smaller link than two copies.
T/TTwo 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.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs12150660
What is rs12150660?
rs12150660 is a single position in the genome, in or near the SHBG 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.
What do people read about alongside rs12150660?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (1 papers), bones and fractures (1 papers), cholesterol and blood fats (1 papers), exercise and muscle (1 papers), fertility (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs12150660 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 rs12150660 come from?
GWAS Catalog, PLoS Genet 2011, PMID:21998597. 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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