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Total testosterone levels

HAFML · rs371162363

What the study found

Who was studied 230,454 European ancestry women.

The effect Each copy of the G allele shifted the measure 0.0392 higher (95% confidence interval 0.029-0.049); p = 6 × 10−15.

How common The G allele had a frequency of about 90% in the people studied.

Where it sits Chromosome 4, band 4q34.3 — in an intron of HAFML.

What each result means

A/A No copy of the version the research linked to Total testosterone levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Total testosterone levels. That is a smaller link than two copies.
G/G 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.
Source

Questions about rs371162363

What is rs371162363?

rs371162363 is a single position in the genome, in or near the HAFML 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 rs371162363 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 rs371162363 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 (rs371162363). MyGeneLog™. https://www.mygenelog.com/variants/rs371162363

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