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Total testosterone levels

MIR3681HG · rs62115715

What the study found

Who was studied 425,097 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0295 higher (95% confidence interval 0.022-0.037); p = 8 × 10−14.

How common The C allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 2, band 2p24.3 — in an intron of MIR3681HG.

What each result means

C/C Two copies of the version the research linked to Total testosterone levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Total testosterone levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Total testosterone levels. This is the starting point the study compared everyone against.
Source

Questions about rs62115715

What is rs62115715?

rs62115715 is a single position in the genome, in or near the MIR3681HG 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 rs62115715 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 rs62115715 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 (rs62115715). MyGeneLog™. https://www.mygenelog.com/variants/rs62115715

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